<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<source>
  <publisher>Regeneron Pharmaceuticals Inc.</publisher>
  <publisherUrl>https://www.regeneron.com/</publisherUrl>
  <lastBuildDate>Tue, 25 Aug 2026 17:02:20 GMT</lastBuildDate>
  <job>
    <title><![CDATA[HVAC Technician (Nights)]]></title>
    <date><![CDATA[Tue, 21 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46924]]></requisitionid>
    <referencenumber><![CDATA[R46924]]></referencenumber>
    <apijobid><![CDATA[r46924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46924/hvac-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an HVAC Technician to join our Facilities Maintenance team. In this role, you will be responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Working hours: Wednesday-Saturday 2:00pm-12:30am</li><li>Training hours: Monday-Friday 8:00am-4:30pm</li><li>Rensselaer, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers.</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work.</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC equipment</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Coordinating with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li></ul><br><h3>This role requires:</h3><ul><li>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level:</li><li>HVAC Technician II: AAS with 2+ years or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years or equivalent combination of education and experience</li><li>HVAC Technician IV: AAS with 8+ years or equivalent combination of education</li><li>Solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>EPA certified for refrigeration gases</li><li>Able to become fully gown qualified to work in production areas</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs (Standard Operating Procedures, cGMPs (current Good Manufacturing Processes), GDPs (Good Documentation Practices) and quality standards</li><li>Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney (Immunology & Inflammation)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47665]]></requisitionid>
    <referencenumber><![CDATA[R47665]]></referencenumber>
    <apijobid><![CDATA[r47665]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47665/director-patent-attorney-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Patent Attorney will work collaboratively with our research and development teams to develop, protect, and manage Regeneron’s valuable intellectual property pertaining to therapeutic molecules. This role will be responsible for patent activities relating to approved and pipeline therapeutic molecules in our Immunology & Inflammation (I&I) therapeutic area.</p><p><strong>This role is based 4 days onsite at Regeneron’s headquarters in Tarrytown, NY and is not open to fully remote work arrangements.</strong></p><p><strong>As a Director, Patent Attorney, a typical day might include:</strong></p><ul><li><p>Identifying and capturing new inventions relating to therapeutic antibodies, formulations of therapeutic antibodies, or methods of treatment based on preclinical or clinical research</p></li><li><p>Working with outside counsel to prepare and prosecute US and international patent applications</p></li><li><p>Managing the implementation of coordinated global patent strategies</p></li><li><p>Assisting in US or foreign patent administrative actions (e.g., post-grant oppositions, post grant reviews)</p></li><li><p>Monitoring clinical programs and continued research and development efforts, including reviewing related planned publications or disclosures</p></li><li><p>Conducting or assisting in patent landscape, freedom-to-operate, or competitive intelligence assessments relating to Regeneron’s therapeutic molecules</p></li><li><p>Assisting in litigation or transactional activities as needed.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Strong organizational skills and the ability to effectively manage multiple projects and competing priorities</p></li><li><p>Ability to work independently and handle a large and complex docket with minimal supervision</p></li><li><p>Excellent oral and written communication skills, including the ability to present complex information accurately and concisely</p></li><li><p>Strong interpersonal skills, including the ability to work effectively and build trust with colleagues and clients at all levels of the organization.</p></li></ul><p><strong>To be considered for this opportunity, you must:</strong></p><ul><li><p>Have a Ph.D. in the life sciences (e.g., molecular biology, cell biology, immunology, biochemistry, or related fields)</p></li><li><p>Have a J.D. from an accredited law school</p></li><li><p>Be admitted to practice before the USPTO and licensed to practice law in at least one state (member of the NY bar or eligible for in-house licensure in NY)</p></li><li><p>Have at least 4-5 years of experience in a law firm and/or corporate law department preparing and prosecuting patent applications in the life sciences</p></li><li><p>Have experience preparing and prosecuting patent applications related to large molecule biologics, especially antibodies.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - TRENTON, NJ]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48012]]></requisitionid>
    <referencenumber><![CDATA[R48012]]></referencenumber>
    <apijobid><![CDATA[r48012]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48012/medical-account-specialist-ii-neurology-trenton-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Trenton]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Trenton (Metro), NJ</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - BALTIMORE, MD]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48015]]></requisitionid>
    <referencenumber><![CDATA[R48015]]></referencenumber>
    <apijobid><![CDATA[r48015]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48015/medical-account-specialist-ii-neurology-baltimore-md/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Baltimore]]></city>
    <state><![CDATA[Maryland]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Baltimore (Metro), MD</li></ul><p><strong> </strong></p><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - FORT WORTH, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48063]]></requisitionid>
    <referencenumber><![CDATA[R48063]]></referencenumber>
    <apijobid><![CDATA[r48063]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48063/medical-account-specialist-ii-neurology-fort-worth-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fort Worth]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Fort Worth (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NEW HAVEN, CT]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48002]]></requisitionid>
    <referencenumber><![CDATA[R48002]]></referencenumber>
    <apijobid><![CDATA[r48002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48002/medical-account-specialist-ii-neurology-new-haven-ct/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New Haven]]></city>
    <state><![CDATA[Connecticut]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: New Haven (Metro), CT</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Nürnberg - Erlangen - Weiden - Regensburg - Ingolstadt - Pfaffenhofen]]></title>
    <date><![CDATA[Thu, 18 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48501]]></requisitionid>
    <referencenumber><![CDATA[R48501]]></referencenumber>
    <apijobid><![CDATA[r48501]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48501/sales-specialist-immunology-fmd-nuernberg-erlangen-weiden-regensburg-ingolstadt-pfaffenhofen/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our ENT (ear - nose - throat) division at key meetings. You will identify the key people in ENT, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><br><p><strong>Where:</strong></p><br><p><strong>Field based in the territory:</strong> <strong>Nürnberg - Erlangen - Weiden - Regensburg - Ingolstadt - Pfaffenhofen</strong></p><br><br><p><strong>Discover your role:</strong></p><br><ul><li>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</li><li>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</li><li>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</li><li>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</li><li>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</li><li>Regular reporting to the sales management</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>Deep understanding of the local healthcare economy, with the ability to identify key players in ENT</li><li>“Patient first” value system</li><li>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech/pharmaceutical sector</li><li>Respiratory experience is preferred</li><li>Proficiency in German as well as conversational English</li><li>Readiness for very frequent travel and a driver's license cl. 3/B.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Clinical Data Reporting]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47783]]></requisitionid>
    <referencenumber><![CDATA[R47783]]></referencenumber>
    <apijobid><![CDATA[r47783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47783/associate-director-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><p>As an Associate Director, Clinical Data Reporting, you will provide leadership and operational oversight for clinical and external data reporting across clinical development programs. You will drive the delivery of high-quality data programming outputs, reconciliation workflows, and reporting solutions that support clinical trial quality, compliance, and informed decision-making.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Leading program-level oversight for clinical data reporting and programming deliverables across development programs</p></li><li><p>Driving development of participant-level listings, exception reports, external data reconciliation outputs, and operational metrics</p></li><li><p>Establishing and maintaining reporting standards, templates, and scalable programming approaches</p></li><li><p>Providing subject matter expertise in data programming, transformation, and visualization to enhance reporting capabilities</p></li><li><p>Collaborating with cross-functional teams to align priorities and ensure timely delivery of reporting outputs</p></li><li><p>Ensuring adherence to regulatory requirements, quality standards, and inspection readiness expectations</p></li><li><p>Driving continuous improvement and automation of reporting workflows</p></li><li><p>Identifying and managing risks related to data quality and delivery timelines</p></li><li><p>Monitoring KPIs to assess reporting performance and enhance processes</p></li><li><p>Leading and mentoring reporting and programming teams to drive operational excellence</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Strong expertise in clinical data management, reporting, and data visualization</p></li><li><p>Experience working with clinical trial data, including eCRF and external data sources such as PK, biomarker, imaging, and ECG</p></li><li><p>Deep understanding of data transformation, validation, and reconciliation processes</p></li><li><p>Strong knowledge of regulatory standards such as ICH-GCP, CDISC, and 21 CFR Part 11</p></li><li><p>Experience with tools such as SAS, R, Tableau, Power BI, Spotfire, or similar reporting platforms</p></li><li><p>Proven ability to work cross-functionally and manage stakeholder expectations</p></li><li><p>Strong analytical, problem-solving, and communication skills</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s degree with 10+ years of relevant experience</p></li><li><p>10+ years of experience in clinical data management or related areas within pharma/biotech</p></li><li><p>At least 5+ years of leadership experience managing teams and mentoring staff</p></li><li><p>Strong experience in clinical data reporting, programming, and analytics</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Delivery and Operations Product Lead – Global Patient Safety]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48288]]></requisitionid>
    <referencenumber><![CDATA[R48288]]></referencenumber>
    <apijobid><![CDATA[r48288]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48288/delivery-and-operations-product-lead-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, the Associate Director, Product Lead for Global Patient Safety sits within the Global Development IT organization, and is a key member of the Delivery & Operations function, responsible for coordinating and guiding their team members in delivering, maintaining & enhancing business solutions. This role partners with key business collaborators to intake, design, implement and improve technology products.</p><p><strong>When & where:</strong> </p><p>This role is based at our Armonk, NY or Warren, NJ location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead implementation, operational support and improvements for Global Patient Safety technology products while guiding Product Analysts and other Delivery & Operations team members.</p></li><li><p>Intake, assess, prioritize, and validate domain specific needs/requirements including partnership with BSPs to ensure alignment between technology roadmaps and product priorities.</p></li><li><p>Act tactically and think strategically, switching leadership styles as needed to influence, guide, and mentor individuals and team.</p></li><li><p>Own end-to-end automating reporting solution, including driving quality and compliance by standardizing report templates, ensuring validated linkages to source data, and automating submission-readiness checks.</p></li><li><p>Harmonize narratives, data structures, and formatting rules to improve report consistency across markets, minimizing regional variability and instilling scientific and regulatory compliance in every output</p></li><li><p>Build relationships with key leaders, partners, and stakeholders to clarify and negotiate (when needed) on demands and solutions.</p></li><li><p>Responsible for identifying resourcing needs and for oversight of internal and vendor delivery, and manage service vendor associates, in support of product.</p></li><li><p>Lead steering committee meetings, working groups, system change requests, issue management, and release management for upgrades to existing product.</p></li><li><p>Accountable for the completion of all necessary project deliverables with responsibility for oversight of Product Analysts, Business Analysts, and other team members as applicable. </p></li><li><p>Responsible for end-to-end product management, including oversight of individual project execution and capability-roadmap planning.</p></li><li><p>Partner with Enterprise IT to help customize service offerings to meet Global Development needs where necessary.</p></li><li><p>Responsible for tracking quantifiable value delivered versus plan and preparing consolidated operational reports summarizing savings.</p></li><li><p>Serves as oversight, quality assurance and escalation point for products within team scope.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors Degree in a related field.</p></li><li><p>At least 10+ years relevant experience, including product owner experience of Global Patient Safety technology solutions (e.g., Argus)</p></li><li><p>Experience working on end-to-end GxP implementations from requirements gathering to IQ and PQ execution</p></li><li><p>Knowledge of the Information Technology Service Management Framework and ITIL v3x</p></li><li><p>Knowledge of Software Development Life Cycle, and agile methodologies and tools (e.g., Jira, Confluence)</p></li><li><p>Strong record of accomplishment of technology project management, stakeholder management, budget management and collaboration skills</p></li><li><p>Experience motivating and building skills within a team of direct reports, instilling a process improvement culture in junior level colleagues.</p></li><li><p>Experience participating in an end-to-end product launch or shut down across multiple teams.</p></li><li><p>Experience hiring, supervising, managing, and mentoring a team in service of complex issues.</p></li></ul><ul><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience</p></li><li><p>Ability to analyze business challenges and present technology solutions</p></li><li><p>Knowledge of pharmaceutical Global Development (e.g., Global Patient Safety, Regulatory Affairs, Clinical Quality) business capabilities, processes, systems, and key trends in the industry</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Information Security - GCC India & JAPAC]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48999]]></requisitionid>
    <referencenumber><![CDATA[R48999]]></referencenumber>
    <apijobid><![CDATA[r48999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48999/director-information-security-gcc-india-japac/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our</strong> <strong>future</strong> <strong>together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are strengthening our global Information Security organization to protect critical business, research, manufacturing, and patient-related assets. We are seeking a Director, Information Security – GCC India & JAPAC to build and lead our India-based Information Security Digital & Technology organization while serving as the regional Information Security leader for JAPAC. In this highly visible leadership role, you will establish a high-performing security organization, drive delivery excellence across multiple security domains, and act as a strategic partner within Regeneron's global security operating model. You will collaborate with senior leadership, regional collaborators, and cross-functional teams to advance security capabilities, manage risk, and ensure regulatory and compliance readiness across a complex global environment.</p><p><strong>When</strong> <strong>&</strong> <strong>where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></p><ul><li><p>Build, lead, and scale the India GCC Information Security organization, fostering a high-performance, inclusive culture focused on accountability, innovation, and continuous improvement.</p></li><li><p>Provide leadership across core security functions including Cyber Operations, Cyber Risk & Assurance, Data Protection & AI Security, Security Architecture, Identity & Access Management, and Attack Surface Management.</p></li><li><p>Lead end-to-end delivery across security engineering, operations, architecture, and data teams applying both agile and traditional delivery models.</p></li><li><p>Drive the adoption and optimization of security technologies including SIEM/SOAR, EDR/XDR, cloud-native security platforms, IAM/PAM, DLP, and vulnerability management solutions.</p></li><li><p>Establish the India GCC security organization as a strategic extension of the global security team, ensuring operational excellence, delivery predictability, and continuous process improvement.</p></li><li><p>Lead recruiting, onboarding, workforce planning, contractor-to-FTE conversions, and capability expansion across security functions.</p></li><li><p>Serve as the JAPAC Information Security lead, representing Regeneron’s security posture to business, regulatory, and partner collaborators throughout the Asia-Pacific region.</p></li><li><p>Design and oversee security governance, risk management, compliance, and control assurance programs aligned with industry frameworks and regulatory requirements.</p></li><li><p>Ensure continuous audit, inspection, and compliance readiness across security programs and technology environments.</p></li><li><p>Partner with executive leaders to translate business objectives into security strategies, investment priorities, and organizational initiatives.</p></li><li><p>Communicate complex security, technology, regulatory, and risk matters to executive, board-level, and operational audiences with clarity and credibility.</p></li><li><p>Evaluate and govern AI and GenAI capabilities to enhance security operations while maintaining compliance, privacy, and governance standards.</p></li></ul><p><strong>This role</strong> <strong>requires:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Information Technology, Cybersecurity, Engineering, or a related discipline.</p></li><li><p>Significant leadership experience managing enterprise Information Security organizations within global companies.</p></li><li><p>Deep expertise across cyber operations, incident response, cyber risk and assurance, data protection, AI security, security architecture, identity and access management, vulnerability management, and attack surface management.</p></li><li><p>Demonstrated success leading security engineering, operations, architecture, and delivery teams in complex global environments.</p></li><li><p>Experience with modern security technologies including SIEM/SOAR, EDR/XDR, cloud security, IAM/PAM, DLP, and vulnerability management platforms.</p></li><li><p>Strong knowledge of security frameworks and regulations including NIST CSF, ISO 27001, SOC 2, GDPR, HIPAA, SOX IT controls, and GxP data integrity requirements.</p></li><li><p>Experience evaluating, implementing, and governing AI and GenAI security capabilities within regulated environments.</p></li><li><p>Proven track record building, scaling, and retaining high-performing technical organizations.</p></li><li><p>Experience establishing or significantly expanding Global Capability Center (GCC) operations, including workforce transformation and organizational growth initiatives.</p></li><li><p>Strong strategic planning, business insight, and decision-making skills with the ability to translate ambiguity into actionable security strategies.</p></li><li><p>Exceptional written, verbal, and executive communication skills with experience engaging senior collaborators across multiple geographies and cultures.</p></li><li><p>Familiarity with APAC information security and privacy regulations, including India's Digital Personal Data Protection (DPDP) Act and related regional requirements.</p></li><li><p>Experience within pharmaceutical, biotechnology, life sciences, or other highly regulated industries.</p></li><li><p>Relevant certifications such as CISSP, CISM, CISA, CCSP, PMP, SAFe, Scrum, or cloud security certifications.</p></li><li><p>Experience operating security programs across multiple jurisdictions and compliance frameworks simultaneously.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47831]]></requisitionid>
    <referencenumber><![CDATA[R47831]]></referencenumber>
    <apijobid><![CDATA[r47831]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47831/director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><div><div><div><div><div><p><strong>Build Our Future Together</strong></p></div></div></div></div></div></div></div></div></div><p>As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is accountable for the delivery of support for one or more research & development programs, within their pharmacometrics discipline. In this capacity the Director is accountable for the timely and accurate delivery of needed quantitative analyses, interpretation, and messaging to PMx management, as well as the timely delivery of well-constructed and well-messaged reports for PMx review.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ, or Cambridge, MA</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects.</p></li><li><p>Works independently, with guidance in only the most complex situations.</p></li><li><p>Informs PMx management of important program and regulatory developments in a timely manner.</p></li><li><p>Ensures analyses and documentation are of the highest quality and accuracy.</p></li><li><p>Ensures that reports and other documents have the appropriate messaging and that a meaningful “story-line” is developed.</p></li><li><p>Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management.</p></li><li><p>Are fully knowledgeable of pharmacokinetic /pharmacodynamic principles, pharmacology, biology, and quantitative aspects of drug development as well as having an advanced knowledge of pharmaceutical drug development.</p></li><li><p>Possess a deep understanding of scientific literature and technical skills in a number of PK/PD methods and techniques. Has extensive knowledge base of the work in overall scientific community in own discipline.</p></li><li><p>Have extensive regulatory experience through authoring of regulatory briefing books, CTD summaries, contribution at HA meetings, HA negotiations through regulatory reviews and approvals of BLA or equivalent.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A PhD and 10+ years with a degree in Quantitative Pharmacology (Pharmacometrics) or related field.</p></li><li><p>Hands on usage of a broad range of quantitative tools and systems is required, as is a strong publication record in the field.</p></li><li><p>Proven experience developing Quantitative Pharmacology elements of regulatory strategy and interacting with regulatory agencies without supervision.</p></li></ul><p>#PMx</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior GD Training Operations Specialist]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48526]]></requisitionid>
    <referencenumber><![CDATA[R48526]]></referencenumber>
    <apijobid><![CDATA[r48526]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48526/senior-gd-training-operations-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The purpose of the <strong>Training Coordinator, Senior Specialist</strong> role is to ensure the smooth and effective execution of training projects by managing and coordinating the intake, development, deployment and collaborating with all key stakeholders to deliver successful learning programs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><p>Location: Armonk, NY or Warren, NJ</p></li><li><p>This role is not eligible remote</p></li></ul><h3><strong>Enable Process and Operational Excellence</strong></h3><ul><li><p>Applies seasoned Training Coordination experience to independently resolve a variety of complex problems that have significant impact on cost or efficiency of training operations</p></li><li><p>Identifies areas for possible improvements and proactively addresses problems within scope of responsibility</p></li><li><p>Regularly makes recommendations on new processes, tools and services that can impact projects in training operations</p></li><li><p>Modifies existing LCoE tools, techniques, and processes, with approval from leadership</p></li><li><p>Regularly contributes actionable ideas in logistics and quality meeting sessions</p></li><li><p>Ability to cross train in other overlapping LCoE areas (ie Onboarding, Training Quality and Compliance)</p></li></ul><h3><strong>Project Management</strong></h3><ul><li><p>Accountable for project lifecycle of a deliverable.</p></li><li><p>Independently tracks and manages key milestones.</p></li><li><p>Determines project and workload priorities</p></li><li><p>Makes recommendations on process improvement and streamlining</p></li><li><p>Invoicing & POs</p></li><li><p>Accountable for PO and Invoice management on the team.</p></li><li><p>Identify areas for improvement in the invoicing process.</p></li><li><p>Identify areas for cost reduction in POs raised</p></li><li><p>Archiving</p></li><li><p>Manage other team members to identify files for archiving at the end of each project.</p></li><li><p>Accountable for material upload</p></li><li><p>Continuously works to improve and automate the archiving process.</p></li><li><p>Demonstrates initiative with new project requests and serves as SME for training coordination and execution</p></li><li><p>Exercises effective interpersonal, communication, training, and problem-solving skills within Training Operations and when interfacing with key stakeholders on project execution</p></li><li><p>With limited guidance, works on moderately complex assignments/projects</p></li><li><p>Supports the Onboarding function of the LCoE team</p></li><li><p>Supports any operational audit initiatives</p></li></ul><h3><strong>UAT</strong></h3><ul><li><p>Performs all UAT testing on LCoE deliverables.</p></li><li><p>Leverage experience, identifies patterns in issues found and makes recommendations on resolution and development process improvement</p></li><li><p>Leverage relationships across the LCoE team to improve outputs.</p></li></ul><h3><strong>Support Training Sessions – Virtual and Face to Face</strong></h3><ul><li><p>Create and manage session schedules, invites, meeting links, rosters and room bookings</p></li><li><p>Reserve meeting rooms with appropriate A/V support for virtual or face to face</p></li><li><p>Coordinate catering and supplies for in person LCoE events</p></li><li><p>Provide online support during live virtual sessions</p></li><li><p>Support instructor logistics, including provision of travel guidelines and attendee rosters, and identifying room set-up/AV requirements.</p></li><li><p>Manage production and delivery of printed course materials where required</p></li><li><p>Manage all pre and post program activities and surveys for both face to face classroom and online training</p></li></ul><h3>This role requires:</h3><ul><li><p>A minimum of a Bachelors' degree and at least 2+ years of relevant experience</p></li><li><p>Preference for prior training operations experience</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Information Technology Operations Analyst]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48882]]></requisitionid>
    <referencenumber><![CDATA[R48882]]></referencenumber>
    <apijobid><![CDATA[r48882]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48882/sr-information-technology-operations-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are seeking a highly motivated and detail-oriented Senior Analyst, Information Technology Operations Management to support the execution and continuous improvement of Information Technology operational processes across Research and Preclinical Development Information Technology (R&pD-IT). This role will ensure reliable service delivery, operational stability, and compliance with enterprise policies and regulatory requirements.</p><p>The Senior Analyst will act as a key liaison between operational teams, engineering, and Information Security/GRC functions, translating enterprise standards into consistent, audit-ready execution. The ideal candidate will bring strong operational expertise, analytical capabilities, and a proactive mindset to improve processes, enhance system reliability, and support a regulated Information Technology environment.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><p>Information Technology Operations Execution</p><ul><li><p>Execute core Information Technology operational processes including system maintenance, patching, monitoring, asset lifecycle management, and service request fulfillment</p></li><li><p>Ensure adherence to standard operating procedures (SOPs) and operational runbooks</p></li><li><p>Support high availability and reliability of infrastructure and applications</p></li></ul><p>Controls, Compliance & Audit Readiness</p><ul><li><p>Execute and monitor operational controls related to system access, asset management, and security compliance</p></li><li><p>Maintain audit-ready documentation and evidence for audits</p></li><li><p>Identify control gaps and partner on remediation</p></li></ul><p>Process Improvement & Optimization</p><ul><li><p>Analyze workflows for inefficiencies and opportunities for automation</p></li><li><p>Drive continuous improvement initiatives</p></li><li><p>Contribute to SOP development and updates</p></li></ul><p>Cross-functional Coordination</p><ul><li><p>Collaborate with Information Technology, engineering, security, and business teams</p></li><li><p>Support shared ownership models and improve handoffs</p></li><li><p>Work with vendors for service delivery</p></li></ul><p>Operational Analytics & Reporting</p><ul><li><p>Track and report key operational metrics (SLAs, uptime, compliance)</p></li><li><p>Perform root cause analysis for incidents</p></li><li><p>Provide insights for improvement</p></li></ul><p>End-User Support & Communication</p><ul><li><p>Support issue resolution and communications</p></li><li><p>Assist with training and documentation</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>5+ years in Information Technology operations or service delivery roles</p></li><li><p>Bachelor’s degree in Information Technology or related field</p></li><li><p>Experience in regulated environments (GxP preferred)</p></li><li><p>Experience in LabIT environments</p></li></ul><p>Technical Skills</p><ul><li><p>Experience with ServiceNow or similar tools</p></li><li><p>Familiarity with monitoring and endpoint tools</p></li><li><p>Experience with reporting and analytics</p></li><li><p>Basic automation/scripting knowledge preferred</p></li></ul><p>General</p><ul><li><p>Strong understanding of Information Technology operations processes (incident, problem, change, asset)</p></li><li><p>Ability to manage multiple priorities</p></li><li><p>Strong communication and analytical skills</p></li><li><p>Detail-oriented with focus on compliance</p></li></ul><p>Domain Knowledge</p><ul><li><p>Information Technology operations lifecycle understanding</p></li><li><p>Operational controls and compliance awareness</p></li><li><p>ITIL familiarity</p></li><li><p>Asset and endpoint management knowledge</p></li><li><p>Incident and problem management experience</p></li></ul><p>Required Licenses & Certificates:</p><ul><li><p>(Optional: ITIL preferred)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - IT Applications Lab Systems]]></title>
    <date><![CDATA[Tue, 21 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47002]]></requisitionid>
    <referencenumber><![CDATA[R47002]]></referencenumber>
    <apijobid><![CDATA[r47002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47002/manager-it-applications-lab-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Manager — Lab Systems (Associate Manager or Manager) to join our IOPS IT team, leading the Laboratory Systems team responsible for the lifecycle development, maintenance, and compliance of laboratory software across our QC, Chemistry, Micro, and Virology labs. In this role, you will oversee system administration, validation, and compliance activities for benchtop and instrument software systems — while collaborating with QA, IT leadership, and cross-functional lab teams to ensure systems are maintained in a compliant and audit-ready state. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Lead and develop the Lab Systems team, overseeing system administration and enhancements for benchtop computer systems and instrument software including Endoscan V, SoftMax Pro, and DataPro2 across the Rensselaer site</li><li>Supervise team performance management and people development activities; serve as technical coach and mentor for direct reports</li><li>Coordinate requirements gathering, system design priorities, and implementation timelines across functional laboratory departments; develop and revise methods, record keeping, policies, and procedures in compliance with regulatory requirements</li><li>Collaborate with QA to ensure validated QC computers and software are maintained in a validated state; implement change control following established procedures and support Laboratory validation activities following SDLC design methodology</li><li>Investigate and resolve computer software and IT hardware issues with QC instrumentation; support preparation of teams for regulatory and internal audits</li><li>Partner with business teams and IT leadership to help develop strategy for a growing organization and team; manage operational budgets and contribute to longer-term Lab Systems planning</li><li>Knowledge of cGMP, GAMP, 21 CFR Part 11, and Annex 11; strong understanding of ALCOA+ principles and data integrity in biopharmaceutical production</li><li>ITIL certification and project management training preferred</li><li>Knowledge of helpdesk ticketing systems such as ServiceNow and Regulatory Asset Manager systems advantageous</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in Information Technology, Science, Engineering, Computer Science, or a related field</li><li>Associate Manager: 6+ years of relevant experience with 2+ years managing teams</li><li>Manager: 7+ years of relevant experience with 3+ years managing teams</li><li>May consider experience in lieu of education. Level is determined based on qualifications relevant to the role</li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - INLAND EMPIRE, CA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48963]]></requisitionid>
    <referencenumber><![CDATA[R48963]]></referencenumber>
    <apijobid><![CDATA[r48963]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48963/medical-account-specialist-ii-hematology-inland-empire-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - California]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: Riverside, Duarte, Loma Linda, Palm Springs</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - KANSAS CITY, MO]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49147]]></requisitionid>
    <referencenumber><![CDATA[R49147]]></referencenumber>
    <apijobid><![CDATA[r49147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49147/medical-account-specialist-ii-hematology-kansas-city-mo/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Kansas City]]></city>
    <state><![CDATA[Missouri]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Kansas City, MO</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - CHICAGO SOUTH, IL]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48950]]></requisitionid>
    <referencenumber><![CDATA[R48950]]></referencenumber>
    <apijobid><![CDATA[r48950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48950/medical-account-specialist-ii-hematology-chicago-south-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: <strong>Chicago - South, IL</strong></p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelor's degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Government Pricing]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46609]]></requisitionid>
    <referencenumber><![CDATA[R46609]]></referencenumber>
    <apijobid><![CDATA[r46609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46609/associate-director-government-pricing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Government Pricing (GP) position is a key member of Regeneron’s government pricing team, which includes supporting the accurate calculation and timely submission of all required government price reporting.</p><p>Included in this role is responsibility for assuring compliance with all pricing and reporting requirements legislated by the Centers for Medicare & Medicaid Services (CMS), the Department of Veterans Affairs and any state legislation required price reporting. This includes a full understanding of all current legislation and staying abreast of pending legislation. Government Pricing Calculations include: Medicaid, Medicare Part B, Public Health Service (PHS)/340B, and Federal Supply Schedule (FSS), which includes: TriCare and the Industrial Funding Fee (IFF). The Associate Director will work collaboratively with Contracting Strategy supporting the overall strategy, contracting and/or payment activities.</p><h3>When & where:</h3><ul><li>Remote with some travel when needed</li></ul><h3>Discover your role:</h3><ul><li>Ability to calculate, validate and report accurate monthly, quarterly, and annual government pricing.</li><li>Submit and monitor State Price Transparency regulations.</li><li>Complete understanding of calculation reasonable assumptions and methodologies and ability to research and communicate cause of variances of results when comparing current period to prior periods.</li><li>Perform all necessary processes needed to ensure compliant submissions including, but not limited to G/L reconciliations, Class of Trade (COT) review, and PHS/340b eligibility review.</li><li>Associate Director will review calculations with Senior Management and obtain approval signoff (and executes any other required Standard Operating Procedures (SOPs)) before communicating prices to the appropriate government agencies (Center for Medicare and Medicare (CMS), Veterans Affairs (VA)/Department of Defense (DOD), etc.) or internally.</li><li>Responsible for maintaining and updating SOP’s and reasonable assumptions, on a quarterly basis, as related to Government Programs/Pricing.</li><li>Monitor policies, procedures and processes supporting Government Pricing submissions and related areas to ensure ongoing compliance with external and internal requirements and guidance.</li><li>Understand and estimate impact of pricing and policy changes regarding government pricing.</li><li>Perform pricing research and analysis on special projects as assigned.</li><li>Ability to review and understand commercial contract language as pertaining to Best Price (BP), Average Sales Price (ASP) and FSS Tracking Customers.</li><li>Investigate Government pricing trends and cross channel impact. Also provide Government price inputs to the Gross to Net (GTN) team.</li><li>Monitor for Tracking customer violations, Bona Fide Service Fee treatments & Customer COT assignment.</li><li>Participate on cross-functional teams as a subject matter expert representing the Government Pricing and Contract Operations as required to evaluate and implement business strategies and initiatives.</li><li>Serve as a liaison with Commercial Leadership, Pricing, Trade, Brand and Accounting/Finance teams regarding a variety of issues impacting government pricing.</li><li>Familiar with Fair Market Value methodology while determining bona fide service fees paid to Wholesaler, Pharmacy Benefit Manager (PBM) and Group Purchasing Organizations (GPOs).</li></ul><h3>This role requires:</h3><ul><li>Bachelors degree and</li><li>7+ years prior experience in Government Pricing OR a related field such as finance, accounting, Medicare/Medicaid</li><li>Strong analytical skills</li><li>10+ years of professional experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing (Neuro)]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47880]]></requisitionid>
    <referencenumber><![CDATA[R47880]]></referencenumber>
    <apijobid><![CDATA[r47880]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47880/associate-director-hcp-marketing-neuro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director of HCP Marketing will lead healthcare professional marketing strategy and execution for the Rare Neurology product in the U.S. This highly visible role requires a forward-looking individual with deep marketing expertise and the ability to navigate a competitive landscape. The Associate Director will partner closely with cross-functional teams to advance the products growth, contribute to the brand's financial success, and help support the launch of the first neurology product at Regeneron.</p><h3>When & where:</h3><ul><li>Office Based for 4 days a week in Sleepy Hollow, NY</li></ul><h3>Discover your role:</h3><ul><li>Contributing and supporting the HCP marketing strategy, ensuring full integration with the broader brand strategy.</li><li>Acting as a key advocate for the brand strategy, clearly articulating priorities and ensuring alignment across Regeneron teams.</li><li>Overseeing the development of HCP engagement strategies, messages, and tactical campaigns tailored to Neurologist.</li><li>Building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</li><li>Driving strong cross-functional and alliance collaboration, partnering with Sales, Medical Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, and HEOR to deliver cohesive, compliant, and impactful initiatives.</li><li>Ensuring all marketing programs comply with corporate policies, regulatory/ethical frameworks, and alliance standards.</li><li>Tracking and managing marketing spend, timelines, and deliverables to meet budget, scope, and performance expectations.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; MBA strongly preferred</li><li>10+ years of progressive experience in the pharmaceutical/biotech industry or related field</li><li>8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas.</li><li>Preferred to have Rare Disease or Rare Neurology experience.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Insights & Analytics - Immunology]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49734]]></requisitionid>
    <referencenumber><![CDATA[R49734]]></referencenumber>
    <apijobid><![CDATA[r49734]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49734/executive-director-commercial-insights-analytics-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director to lead our <strong>Commercial Insights and Analytics (I&A), Immunology</strong> team.</p><p>The Executive Director, Commercial Insights and Analytics (I&A), Immunology, will report directly into the Vice President, Commercial Strategy and Insights & Analytics (CSI&A) within the CSI&A department. This role will lead the high-performing I&A team responsible for the Immunology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions across some of Regeneron’s leading brands. The role will partner with and serve as a strategic advisor for the SVP, Commercial Immunology CBU, and will partner with other leaders to grow and develop talent within the I&A organization.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Immunology team in providing business analytics, customer insights and competitive intelligence to deliver rich insights to solve key business problems </p><p>2) Set the strategic I&A direction that aligns with CBU priorities and helps drive commercial excellence </p><p>3) Serve as a member of the Immunology CBU Leadership Team, providing I&A expertise </p><p>4) Serve as a member of the CSI&A leadership team to drive cross-commercial innovation and best-in-class delivery </p><p><em>Develop</em></p><p>5) Translate complex analyses into compelling insights and recommendations that will be used to inform business decision-making for senior Regeneron teams, including the CBU, Chief Commercial Officer, Chief Executive Officer and Board of Directors </p><p>6) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent </p><p>7) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform brand differentiation, market growth and business impact; and <strong>b)</strong> consider business potential for pipeline products </p><p><em>Partnership and Collaboration</em></p><p>8) Collaborate with the Immunology CBU and other members of senior leadership to contribute to ongoing brand strategies and decisions, including long-term data, analytics and insights roadmap</p><p>9) Develop and maintain a mutually beneficial partnership with CBU stakeholders; ensure insight generation and feedback are embraced; strike a balance between project rigor, timelines and ability to influence decisions</p><p>10) Lead efforts to identify and crystalize insights that inform strategic plans for the Immunology CBU </p><p>11) Work with other CSI&A leaders to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analyses, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>12) Proactively communicate with the Immunology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>13) Construct and deliver integrated business reviews, I&A summary overviews with the Immunology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>This role requires:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with buy-and-bill brands in highly competitive markets is required</p></li><li><p>Minimum Bachelor’s degree in data science, public health, statistics, engineering, or a related field</p></li><li><p>Functional expertise in business analytics, customer insights, analog forecast development, market access, and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, customer insights, market access analytics, and competitive intelligence</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution with hands on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li><li><p>Master’s (MBA, MPH, MS) preferred</p></li><li><p>Experience with co-promotes, as well as the immunology disease category, is strongly desired</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Inspection Readiness]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47671]]></requisitionid>
    <referencenumber><![CDATA[R47671]]></referencenumber>
    <apijobid><![CDATA[r47671]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47671/senior-manager-clinical-study-inspection-readiness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Study Inspection Readiness to join our Clinical Trial Management function, supporting inspection readiness across one or more assigned clinical programs. In this role, you will lead GCP inspection readiness strategy and serve as the primary point of contact for all inspection-related activities, while collaborating closely with Program Operations Leaders, Clinical Study Leads, CRO partners, and Inspection Management.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Armonk, NY, Warren, NJ</p></li><li><p>Travel percentage: Up to 25%</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead GCP inspection readiness programs across complex, multi-program portfolios spanning internal teams, CRO partners, and Inspection Management</p></li><li><p>Own the inspection process end-to-end — mock, dry run, and actual — managing follow-up requests from inspectors and inspection management teams</p></li><li><p>Partner with Clinical Study Teams and functional areas to prepare Q&A responses and drive action items to closure</p></li><li><p>Guide CTM staff on compliance with SOPs, Business Practice Tools, and Work Instructions throughout the study lifecycle</p></li><li><p>Track inspection readiness meetings, action items, storyboards, and presentation requests with internal and CRO stakeholders through resolution</p></li><li><p>Manage the full inspection action item lifecycle — from pre-inspection readiness through post-inspection remediation, timelines, and closure — ensuring a complete audit trail</p></li><li><p>Champion use of AI-powered tools to accelerate high-quality deliverables, from executive summaries and storyboards to CAPA narratives and TMF gap analyses</p></li><li><p>Coach, develop, and set goals and accountabilities for direct reports, reviewing performance against quality and timeliness standards</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA degree and 8+ years of relevant clinical experience</p></li><li><p>Strong project management instincts, especially under the pressure of live inspection timelines</p></li><li><p>Preferred: hands-on clinical inspection experience (mock, dry run, or actual regulatory inspections)</p></li><li><p>Preferred: experience partnering with CROs and cross-functional clinical study teams</p></li><li><p>Preferred: familiarity with AI-powered productivity tools (e.g., Claude, Microsoft Copilot) in a documentation or compliance context</p></li><li><p>Proactive risk thinking — identifying Sites of Interest and documentation gaps before they become findings</p></li><li><p>Clear, confident communication across internal teams, CRO partners, and inspectors</p></li><li><p>Comfort leading and coaching others while staying hands-on with the details</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, Neurology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48596]]></requisitionid>
    <referencenumber><![CDATA[R48596]]></referencenumber>
    <apijobid><![CDATA[r48596]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48596/senior-medical-director-medical-affairs-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Neurology/Myasthenia Gravis Medical Affairs Team. The Senior Medical Director is responsible for the co-development of medical strategy and planning & execution of medical affairs activities at Regeneron. This hire will provide medical leadership and serve as a key scientific/medical resource.</p><p>The Senior Medical Director will report to Head of Medical Affairs, Neurology and work in a cross-functional, matrix organization. He/she will also collaborate with external stakeholders such as healthcare practitioners, key opinion leaders and payers.</p><p><strong>When & where:</strong></p><ul><li>Location: Sleepy Hollow, New York; Warren, New Jersey; or Cambridge, Massachusetts <em>*If hired in Warren, NJ or Cambridge, MA, frequent travel to Sleepy Hollow, MA may be required*</em></li><li>Travel: 25% to relevant conferences and congresses</li></ul><p><strong>Discover your role:</strong></p><ul><li>Maintain deep scientific and medical knowledge of Neurology / Myasthenia Gravis, treatment landscape and clinical decision making</li><li>Function as an integral member of the cross-functional Medical Team</li><li>Responsible for data generation, data analyses and interpretation as it relates to Phase 4 studies, including interventional and observational research</li><li>Responsible for the medical content of post-marketing study reports, analyses of clinical data, safety monitoring, and activities that ensure patient safety</li><li>Provide scientific and medical support for development of strategic medical, publications, communications and integrated evidence generation plans</li></ul><ul><li>Participate in developing and presenting medical content at congresses, symposia and advisory boards</li><li>Proactively bring patients' & physicians' voice on cross-functional teams, to enable effective and impactful decision making</li><li>Provide medical training for internal staff on investigational and/or approved products, disease state and unmet needs</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>An M.D. or equivalent with board eligibility or board certification in Neurology strongly preferred</li><li>A minimum of 8 years Pharmaceutical / Biotech industry experience (launch experience is preferred)</li><li>Direct experience in Myasthenia Gravis or Neurology Rare Disease is strongly preferred</li></ul><ul><li>Experience and ability in working in a dynamic, matrix environment; excellent collaboration and communication skills</li><li>Ability to demonstrate deep understanding of all medical affairs accountabilities</li><li>Thorough understanding of Neurology and Myasthenia Gravis healthcare environment and key stakeholders</li></ul><p>#MDJobs, #MDJobsMA, #GDMAJobs, #Neurology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager R&D Procurement]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48236]]></requisitionid>
    <referencenumber><![CDATA[R48236]]></referencenumber>
    <apijobid><![CDATA[r48236]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48236/associate-manager-rd-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager Global Procurement R&D Lab Consumables to join our Global Procurement team, supporting our Lab Consumables category in a hybrid work model. In this role, you will support category strategy development, strategic sourcing, supplier management, data-driven decision making, and cost optimization initiatives while collaborating with partners, suppliers, Procurement colleagues, the Law department, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Support the definition and implementation of global Lab Consumables category strategies that serve regional and global business needs.</p></li><li><p>Partner with collaborators and Procurement leadership to align category priorities and manage category-related discussions.</p></li><li><p>Lead sourcing activities, negotiations, supplier management, stakeholder engagement, and contracting initiatives for assigned Lab Consumables categories.</p></li><li><p>Drive value through cost savings, cash flow improvements, inventory insights, and broader category management efficiencies using spend and performance analytics.</p></li><li><p>Negotiate contract terms and conditions in collaboration with the Law department while ensuring alignment with business requirements.</p></li><li><p>Ensure category activities align with applicable GxP requirements and other relevant regulations while supporting supplier performance and service delivery.</p></li><li><p>Use market intelligence, benchmarking, supplier engagement, and data analytics to inform decisions and strengthen category outcomes.</p></li><li><p>You bring integrity, focus, and collaboration to help drive continuous improvement and positive outcomes across teams and supplier partnerships.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field of study and progressive procurement experience, including experience in Pharma or BioPharma.</p></li><li><p>Experience managing category processes and suppliers across a breadth of categories.</p></li><li><p>Demonstrated success working with cross-functional teams to deliver results in Lab Consumables or related categories through sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Experience providing insights on rates, unit costs, costing structures, cost models, and total cost of ownership models to support effective negotiations and sourcing decisions.</p></li><li><p>Experience using external data sources, market intelligence, supplier engagement, and supply market insights to evaluate sourcing opportunities and market dynamics.</p></li><li><p>Demonstrated success supporting global supply market evaluations using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Experience supporting supplier relationship management activities and building productive collaborator and supplier partnerships.</p></li><li><p>Working knowledge of sourcing and contracting tools, Enterprise Resource Planning (ERP) systems, and electronic Request for Proposal (eRFX) platforms, including Oracle, Zycus, Ariba, or similar systems.</p></li><li><p>Working knowledge and hands-on experience supporting sourcing platform technologies such as LabViva, Zageno, Science Exchange, Scientist.com, or similar platforms.</p></li><li><p>Ability to employ Word, Excel, and PowerPoint for communication, analysis, and presentations</p></li><li><p>Experience using data analytics, automation, and visualization tools such as Power BI, Tableau, and Power Automate to generate insights and communicate recommendations to partners and senior leadership.</p></li><li><p>Experience implementing inventory management programs and supporting technologies, including RFID, QR code solutions, consignment programs, vendor-managed inventory, single-use materials, bioreagents, and media.</p></li><li><p>Experience operating with integrity, focus, and clarity in ambiguous environments while motivating change and improvement.</p></li><li><p>Experience managing associate-level professionals preferred.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager -Indirect Category Management]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48246]]></requisitionid>
    <referencenumber><![CDATA[R48246]]></referencenumber>
    <apijobid><![CDATA[r48246]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48246/associate-manager-indirect-category-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager Indirect Category Management Procurement to join our Global Procurement team, supporting our Indirect Procurement categories in a hybrid work model. In this role, you will support category strategy development, sourcing activities, supplier evaluation, spend analysis, and category management enablement while collaborating with category teams, data and analytics teams, partners, and suppliers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Support the definition and implementation of indirect category strategies across Information Technology, Professional Services, Human Resources Services, and Travel & Meetings categories.</p></li><li><p>Support category teams in developing and implementing category strategies through market analysis, spend analysis, supplier evaluation, and risk management activities.</p></li><li><p>Maintain standardized category management templates, strategy decks, stage gate presentations, and repository materials to drive consistency across category teams.</p></li><li><p>Partner with data and analytics teams to employ internal and external data sources to identify trends, opportunities, and strategic insights.</p></li><li><p>Facilitate sourcing activities by supporting Requests for Information (RFI), Requests for Quotation (RFQ), and Requests for Proposal (RFP) processes, including response collection and analysis.</p></li><li><p>Summarize sourcing and supplier relationship management outcomes through comparative analysis of supplier responses, pricing, and evaluations.</p></li><li><p>Maintain category plans, opportunity analyses, presentations, supplier relationship management materials, and other category documentation within the central repository.</p></li><li><p>You bring a collaborative and improvement-focused attitude while supporting compliance activities, audit requests, procurement process enhancements, and category development initiatives.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field of study and progressive experience in procurement; experience within Pharma or BioPharma preferred.</p></li><li><p>Strong knowledge of category management principles, including sourcing, procurement, planning, supplier interactions, and negotiations.</p></li><li><p>Working knowledge of Enterprise Resource Planning (ERP) systems such as Oracle.</p></li><li><p>Experience with Source-to-Pay (S2P) platforms including Oracle, Zycus, Sievo, GEP, Ariba, or similar platforms preferred.</p></li><li><p>Proficiency in Word, Excel, and PowerPoint for communication, presentations, and data analysis.</p></li><li><p>Experience with spend analytics software preferred.</p></li><li><p>Excellent verbal and written English communication skills with the ability to present effectively to customers.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-Oncology-Mobile, AL - Tallahassee, FL]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49771]]></requisitionid>
    <referencenumber><![CDATA[R49771]]></referencenumber>
    <apijobid><![CDATA[r49771]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49771/medical-account-specialist-ii-oncology-mobile-al-tallahassee-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mobile]]></city>
    <state><![CDATA[Alabama]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where:</strong></p><ul><li><p>Field role</p></li><li><p>Reside in the Pensacola Territory (Mobile, AL - Tallahassee, FL)</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists.</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelors degree; Master’s degree or additional advanced education/certifications a plus.</p></li><li><p>Minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred).</p></li><li><p>Buy and bill experience with biologics required.</p></li><li><p>Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions.</p></li><li><p>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks.</p></li><li><p>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization.</p></li><li><p>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p></li></ul><p><strong>Salary range (annually)</strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist, Oncology Sales - Minneapolis, MN]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49682]]></requisitionid>
    <referencenumber><![CDATA[R49682]]></referencenumber>
    <apijobid><![CDATA[r49682]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49682/medical-account-specialist-oncology-sales-minneapolis-mn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minneapolis]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Minneapolis, MN</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them</p></li></ul><p>​</p><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred)</p></li><li><p>Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions</p></li><li><p>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. </p></li><li><p>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace</p></li><li><p>You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization</p></li><li><p>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Must have ability to travel and cover large geography territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Specialist Global Procurement]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49038]]></requisitionid>
    <referencenumber><![CDATA[R49038]]></referencenumber>
    <apijobid><![CDATA[r49038]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49038/sr-specialist-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior Specialist Global Procurement </strong>to join our <strong>Procurement </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Supporting the definition and implementation of the global Direct Category strategy to serve global and regional business needs</p></li><li><p>Assisting negotiations, supplier management activities, and stakeholder engagement activities for the Direct Category as assigned</p></li><li><p>Generating value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities</p></li><li><p>Supporting Global Procurement by participating in decisions with critical short and long-term impact on the success, efficiency, growth, and results of the category team</p></li><li><p>Demonstrating knowledge of efficient global procurement organisations and processes within the biopharmaceutical industry to support the growth and evolution of the Procurement organisation and using this knowledge to drive improvements within Regeneron</p></li><li><p>Contributing to category activities to ensure compliance with appropriate GxPs and other applicable regulations, as applicable</p></li><li><p>Using data to drive decision-making for successful category projects</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Establishing relationships with stakeholders and suppliers to get results for Regeneron</p></li><li><p>The candidate should demonstrate success supporting cross-functional teams to drive results through effective sourcing, negotiations, contracting, and supplier relationship management</p></li><li><p>Providing insights on rates, unit costs, and costing structures for efficient negotiations</p></li><li><p>Use external data sources, market information, and supplier engagement to constantly improve Regeneron’s knowledge of supply market dynamics</p></li><li><p>Experience operating with integrity, focus, and clarity in an environment of ambiguity to inspire change and improvement</p></li><li><p>Proven success supporting the global supply market evaluation process using all available market intelligence, risk, compliance, and financial assessment tools</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>The role requires a bachelor's degree in a relevant field of study plus relevant, progressive experience in procurement, including experience in Pharma/BioPharma</p></li><li><p>You are proficient with sourcing contracting tools, ERP’s, and eRFx systems preferred (Oracle, Zycus, Ariba, Other)</p></li><li><p>Ability to harness standard business applications for communicating, presenting and analyzing data (Word, Excel, Powerpoint).</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIE</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Compliance Specialist, Engineering & Automation]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49536]]></requisitionid>
    <referencenumber><![CDATA[R49536]]></referencenumber>
    <apijobid><![CDATA[r49536]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49536/compliance-specialist-engineering-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re looking for a Compliance Specialist focusing on engineering and automation. This position ensures and supports cGMP and procedural compliance for our Technical Operations Engineering & Automation Department. This includes conducting evaluations against documents and providing guidance to others on a variety of cGMP work. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm </li></ul><p><strong>What you’ll do:</strong></p><ul><li> Maintain up-to-date knowledge of cGMPs and Biotech/Pharmaceutical industry guidance (including emerging draft GxP guidance), and evaluate department practices against these standards</li><li>Support the authorship, review, and follow-through of department documentation and records, including change controls, investigations, root cause analyses, risk assessments, impact statements, CAPAs, SOPs/work instructions/job aids, periodic evaluation reports, logbooks, maintenance records/work orders, lifecycle documents, and policies</li><li>Serve as liaison between Engineering & Automation and Quality/Regulatory groups to identify and resolve compliance issues</li><li>Identify continuous improvement opportunities and support or lead related initiatives</li><li>Support audit/inspection coordination, author responses, and track/trend results across department quality, compliance, and regulatory audits/inspections</li><li>Maintain strong knowledge of cGMP biotech/pharma manufacturing operations and laboratory testing, regulatory and quality requirements/guidance, and root cause and risk management techniques, procedures, and documentation methods</li><li>Manage multiple tasks and meet deadlines</li><li>Present to large groups, including senior management and regulatory agencies</li><li>Communicate clearly and professionally in writing and interpersonal interactions</li><li>Apply working knowledge of word processing, spreadsheet, presentation, and database management software</li></ul><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Requires B.S in life sciences, engineering or related field; or equivalent combination of education and experience <ul><li>Associate Compliance Specialist: 0-2+ years of experience</li><li>Compliance Specialist: 2+ years of experience</li><li>Senior Compliance Specialist: 5+ years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Drug Product MSAT Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48564]]></requisitionid>
    <referencenumber><![CDATA[R48564]]></referencenumber>
    <apijobid><![CDATA[r48564]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48564/senior-drug-product-msat-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is seeking a Senior Drug Product (DP) Manufacturing Sciences and Technology (MSAT) Specialist to join our Process Science Drug Product Engineering department. The Drug Product Manufacturing Science and Technology (MSAT) Engineer supports equipment selection, management of equipment qualification, and process validation activities, and will be responsible for solving issues during technology transfer and cGMP start-up for internal or external manufacturing sites. They also provide on the floor support during operations, as needed, for internal or external manufacturing, reviews process data to ensure operational consistency, and provides support for investigations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li><li>Travel percentage: 25-50% domestic & occasionally international</li></ul><p><strong>Discover your role:</strong></p><ul><li>Provides drug product manufacturing process knowledge for new product introduction, technology transfer, process validation, process troubleshooting and issue resolution for biopharmaceutical drug products</li><li>With the support of multi-functional teams, acting as the technical lead, for technology transfer of the drug product manufacturing processes to manufacturing facilities</li><li>Tracking and reporting project milestones related to raw material/component procurement, equipment readiness, process transfer, manufacturing document creation, etc.</li><li>Reviewing and approving cGMP batch documentation (master batch records, component specifications, validation protocols, material specifications, etc.) required to support cGMP production at manufacturing facilities</li><li>Assisting with investigation and root cause determination and CAPA identification and implementation for manufacturing deviations</li><li>Trending process performance and collaborates with internal and external teams to establish/improve process performance, process capability to ensure process is operating within intended process control strategy</li><li>Authoring technical reports/protocols in support of cGMP activities</li><li>Supporting development of sampling plans for cGMP batches related to process characterization, process qualification, lot release, stability etc.</li><li>Assisting in equipment selection, qualification, and start up activities and working with manufacturing to ensure robust procedures are used for operation of equipment</li><li>Partnering with strategic sourcing/procurement to specify technical requirements associated with raw materials, components, equipment and services to ensure external vendor on time delivery</li><li>Supporting the drafting of regulatory filings and responding to regulatory information requests</li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering; chemical engineering or biomedical engineering preferred and 5+ years of relevant experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Device Development Engineer]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49477]]></requisitionid>
    <referencenumber><![CDATA[R49477]]></referencenumber>
    <apijobid><![CDATA[r49477]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49477/senior-device-development-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Device Development Engineer to join our New Technologies, Combination Products Innovation team. This engineer will be responsible for front-end innovation projects and scenario planning to support Regeneron’s growing pipeline, working cross-functionally to define patient, user, and business needs, identify and advocate for novel device solutions and opportunities, and manage early-stage device design and development programs.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead and influence drug-device combination product scenario planning for new and lifecycle management programs, collaborating cross-functionally to gather stakeholder input, drive strategic decisions, and gain buy-in on long-term device strategies within therapeutic areas</li><li>Research, monitor, and analyze drug delivery system industry and market trends, competitive landscapes, internal pipeline drug delivery needs, and patient/user needs to identify innovation opportunities and advise device strategy</li><li>Perform technical feasibility evaluations and due diligence assessments, working with external strategic partners to drive toward innovative device solutions</li><li>Lead early-stage drug delivery system design efforts with a multi-functional team, translating business needs and stakeholder requirements into comprehensive project plans and innovative product design</li><li>Generate insights through exploratory, user, and foundational research to inform the drug delivery system portfolio, collaborating with technical teams, human factors, commercial, clinical, and other subject matter experts as applicable</li><li>Maintain a culture of continuous improvement that strives to ensure safety and efficacy while accelerating delivery of commitments</li><li>Represent Regeneron and the device teams at appropriate industry meetings and forums</li><li>Demonstrate strong communication, presentation skills and can strategic alignment</li><li>Possess project management skills and can work effectively across multiple functional teams</li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering field; Biomedical Engineering or Mechanical Engineering is preferred<ul><li>Device Development Engineer: 2+ years of experience</li><li>Sr. Device Development Engineer: 5+ years of experience</li><li>Experience with design history file management (21 CFR 820.30)</li><li>Experience with delivery device branding/marketing is preferred </li></ul></li><li>Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Specialist LCoE Operations]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49941]]></requisitionid>
    <referencenumber><![CDATA[R49941]]></referencenumber>
    <apijobid><![CDATA[r49941]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49941/sr-specialist-lcoe-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist Learning Center of Excellence Operations - India to join our Learning Center of Excellence team, supporting our India Global Capabilities Center and regional learning initiatives in a hybrid work model. In this role, you will support regional training, onboarding, and learning delivery while collaborating with Regional Trainers, Training Business Partners, Human Resources, functional leaders, and onboarding teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Develop and adapt regional training programs and learning materials, ensuring content is localized, culturally relevant, and aligned with business needs.</p></li><li><p>Co-facilitate in-person and virtual training sessions, including systems, business process, functional onboarding, and role-specific learning programs.</p></li><li><p>Serve as a regional Learning Center of Excellence contact, responding to training requests, onboarding inquiries, and stakeholder needs when required.</p></li><li><p>Coordinate onboarding activities with Human Resources, functional leaders, and global onboarding teams to deliver a seamless new-hire experience for GCC colleagues.</p></li><li><p>Create, update, and maintain onboarding content including videos, reference guides, help materials, training communications, and SharePoint onboarding pages.</p></li><li><p>Administer Learning Management System activities including registrations, attendance reporting, scheduling coordination, and risk issue related to training plans.</p></li><li><p>Promote learning events, build networks of subject matter experts, and encourage strong engagement with training initiatives across the region.</p></li><li><p>You foster collaboration across global and local teams while continuously seeking opportunities to improve learning experiences and onboarding effectiveness.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Demonstrated experience creating training plans, curricula, and learning materials across multiple delivery modalities.</p></li><li><p>Experience supporting training design, development, facilitation, onboarding, and stakeholder engagement activities.</p></li><li><p>Ability to co-facilitate virtual and in-person training programs, including technical, functional, and onboarding learning sessions.</p></li><li><p>Experience developing and maintaining training content, onboarding resources, videos, reference guides, help documentation, and related learning assets.</p></li><li><p>Experience administering Learning Management System processes, including registration management and attendance reporting.</p></li><li><p>Experience managing SharePoint onboarding or learning-related sits and content repositories.</p></li><li><p>Ability to support the development of functional learning solutions using artificial intelligence and learning development applications.</p></li><li><p>Fluency in English and the language of the assigned region.</p></li><li><p>Ability to travel up to 25% as required.</p></li><li><p>Strong facilitation, presentation, communication, and collaboration skills.</p></li><li><p>Proven ability to coordinate projects, plan and execute initiatives, and work successfully within a matrix organization.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Pharmacovigilance Hub]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47624]]></requisitionid>
    <referencenumber><![CDATA[R47624]]></referencenumber>
    <apijobid><![CDATA[r47624]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47624/director-pharmacovigilance-hub/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director, Pharmacovigilance Hub</strong> to join our <strong>Global Patient Safety Operations</strong> team. The Director, PV Hub oversees country and/or regional level PV execution within their assigned region and ensures that local safety activities are performed in accordance with global standards, local regulatory requirements are met, and all country-generated safety data are accurately and timely integrated into the global PV system. This role serves as the escalation point for local execution issues and as the conduit between local operations and global oversight functions. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Maintain a comprehensive understanding of local legislation and Health Authority requirements and keep Worldwide Operations Office (WWOO) leadership informed of updates or changes to local requirements or processes (e.g., SOP addenda, safety communications, labeling updates, and local submission requirements) in alignment with country-specific regulatory requirements </p></li><li><p>Track local process status, changes, and risks to drive consistency and continuous improvement for hub’s geographic markets, including maintaining and monitoring via common tool (e.g., tracker, dashboard) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Ensure country compliance with the global PV quality system, supporting inspections, audits, CAPAs, and timely resolution of deviations or non-compliance </p></li><li><p>Serve as local safety PoC to coordinate with global GPS (e.g., PV Enablement, CER, SS) and non-GPS (e.g., Med Affairs, Regulatory) teams to: </p></li><li><p>Guide and inform global teams on local requirements and ensure compliance with local legislations </p></li><li><p>Coordinate with other PV hub(s) as needed for contributions to activities and/or local documentation </p></li><li><p>Shape compliant programs that provide high quality adverse event reports </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum Bachelor’s Degree (Advanced Degree preferred) with 12+ years of PV experience and demonstrated achievements in patient safety</p></li><li><p>Experience supporting regulatory inspections, audits, and quality issue management at the country or regional level </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Ability to coordinate across functions and cultures, operating effectively as an execution and escalation lead rather than a policy owner </p></li><li><p>Strong organizational and communication skills, with the ability to surface local risks early and drive resolution through global governance channels </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior QA Validation Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48401]]></requisitionid>
    <referencenumber><![CDATA[R48401]]></referencenumber>
    <apijobid><![CDATA[r48401]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48401/senior-qa-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Senior QA Validation Specialist</strong> to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><ul><li>Location: Raheen, Limerick</li><li>Some travel may be required.</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Generating, executing and/or reviewing master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria</li><li>Analysing the results of testing and determines the acceptability of results against pre-determined criteria</li><li>Investigating and troubleshooting problems which occur and determines solutions or recommendations for changes and/or improvements</li><li>Reviewing, editing and approval deviation notifications, deviation investigations, and corrective actions</li><li>Reviewing and approval of change controls, SOPs, reports and other documentation</li><li>Coordinating with other departments or outside contractors/vendors to complete validation tasks</li><li>Managing projects and prepares status reports</li><li>Providing oversight to contingent workers may be a requirement</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Ability to work independently or as part of a team</li><li>Ability to communicate with transparency</li><li>Meets commitments on scope and on time</li><li>Follows directions, performs well-defined tasks</li><li>Effective time management skills</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>To be considered for this opportunity you must have a BS/BA in Engineering, Chemistry or Life Science and requires at least 5 – 8+ years’ proven experience in Commissioning / Qualification experience with Large Scale Process equipment </li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQA </strong><strong>#REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49351]]></requisitionid>
    <referencenumber><![CDATA[R49351]]></referencenumber>
    <apijobid><![CDATA[r49351]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49351/principal-qa-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Principal QA Specialist </strong>to join our <strong>QA Compliance & Quality Systems </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Serving as a Quality Systems Subject Matter Expert (SME) with primary responsibility for Change Control governance, oversight, and continuous improvement activities.</p></li><li><p>Providing quality and compliance oversight of Quality System processes, including but not limited to: Change Control, Deviations, CAPA's, Audits, Customer Complaints and Risk Management.</p></li><li><p>Ensuring Quality System records are managed in compliance with regulatory requirements, company procedures, and data integrity expectations.</p></li><li><p>Reviewing and approving Quality System documentation, including Change Control records, Deviation investigations, CAPA plans and Risk assessments.</p></li><li><p>Leading or supporting governance forums, review boards, and cross-functional meetings associated with Change Control and Quality System management.</p></li><li><p>Monitoring, analysing, and communicating Quality System performance metrics and trends, finding opportunities to improve process effectiveness, efficiency, and compliance.</p></li><li><p>Performing quality review of complex, high-impact, and cross-functional changes to ensure appropriate assessment of product quality, regulatory, validation, and operational impacts.</p></li><li><p>Supporting regulatory inspections and customer audits, including preparation activities, presentation of Quality System processes, and response development for observations or commitments.</p></li><li><p>Identifying compliance risks, process gaps, and systemic issues within Quality Systems and leads or supports development and implementation of sustainable corrective actions.</p></li><li><p>Collaborating with Manufacturing, Quality Control, Engineering, MSAT, Supply Chain, Validation, Regulatory Affairs, and other site functions to ensure quality and compliance requirements are effectively integrated into business processes.</p></li><li><p>Leading and participating in continuous improvement initiatives aimed at enhancing Quality System performance, inspection readiness, and operational excellence.</p></li><li><p>Supporting the development, implementation, and maintenance of Quality System procedures, policies, and training programs.</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>Experience working with Quality Systems, including one or more of the following: Change Controls, Deviations, CAPA's, Audit Management and Risk Management</p></li><li><p>Working knowledge of cGMP requirements and regulatory expectations.</p></li><li><p>Strong organisational, communication, and stakeholder management skills, with the ability to effectively coordinate activities across multiple functional areas.</p></li><li><p>Able to prioritise, re-prioritise as needed and adapt to change.</p></li><li><p>Comfortable working in a fast-paced setting.</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>Requires BSc/BEng in scientific discipline or related field with 7+ years of relevant work experience in pharmaceutical or related industry.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - Chicago N, IL]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49629]]></requisitionid>
    <referencenumber><![CDATA[R49629]]></referencenumber>
    <apijobid><![CDATA[r49629]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49629/medical-account-specialist-ii-hematology-chicago-n-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: Chicago, North</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Monday-Friday 1st Shift]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47634]]></requisitionid>
    <referencenumber><![CDATA[R47634]]></referencenumber>
    <apijobid><![CDATA[r47634]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47634/calibration-technician-monday-friday-1st-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Calibration Technician</strong> to join our <strong>Technical Operations </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Shift Requirements: Monday - Friday 08.00am - 4.30pm</p></li><li><p>Location: Rensselaer, New York</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Calibrating various types of instrumentation including temperature, pressure, level, flow and analytical instruments</p></li><li><p>Performing loop check, tune, troubleshoot, and start-up of instrumentation</p></li><li><p>Working with medium and low voltages</p></li><li><p>Performing basic plumbing and tube bending jobs</p></li><li><p>Assisting the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</p></li><li><p>Performing daily Work Orders (WO) and Preventative Maintenance (PM) and efficiently coordinate the workflow and documentation of PMs and WOs</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</p></li><li><p>Following current Good Manufacturing Practices (cGMPs)</p></li><li><p>Occasionally working on other facility related work tasks/issues that are outside the calibration department’s normal work duties</p></li><li><p>May include planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</p></li><li><p>Participation in compliance investigations if and when necessary</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Ability to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li><li><p>Full gowning required when entering and working on production floor</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p></li></ul><p>Calibration Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p><p>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p><p>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p><p>Level will be determined based on qualifications relevant to the role</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p>#REGENTOSK </p><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Manufacturing Sciences & Technology Engineer]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49407]]></requisitionid>
    <referencenumber><![CDATA[R49407]]></referencenumber>
    <apijobid><![CDATA[r49407]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49407/principal-manufacturing-sciences-technology-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking a Principal MSAT Engineer to join our Process Sciences Drug Product Engineering department. This role supports and/or leads equipment selection, CMO selection strategy, management of equipment qualification and/or process validation activities and will be hands-on solving issues during technology transfer and cGMP start-up. The MSAT team establishes best practices for technical support of cGMP drug product manufacturing operations. The Engineer also provides floor support during operations of internal or external manufacturing, reviews process data to ensure operational consistency after processes are successfully transferred and provides support for investigations.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm </li><li>Travel percentage: 25-50% domestic & occasionally international</li></ul><p><strong>Discover your role:</strong></p><ul><li>Serves as technical lead and subject matter expert for drug product manufacturing process transfer, providing oversight for new product introduction, technology transfer, and process troubleshooting/issue resolution</li><li>Tracks and reports project milestones (raw material/component procurement, equipment readiness, analytical transfer, documentation) and partners with/leads cross-functional internal and external teams to ensure successful transfer execution</li><li>Reviews and approves cGMP batch documentation (master batch records, specifications, validation protocols) and authors policies, technical reports, protocols, and change controls in support of cGMP activities</li><li>Monitors cGMP compliance at drug product contract manufacturers to protect product integrity and company reputation</li><li>Trends process performance to establish and improve process capability, ensuring operations remain within the intended control strategy</li><li>Investigates deviations, determines root cause, and identifies/implements CAPA; develops sampling plans for GMP batches (lot release, stability, characterization)</li><li>Collaborates with internal/external teams to identify and drive opportunities for improved process performance and cGMP operations</li><li>Leads or assists in equipment selection, qualification, and start-up activities, and works with Manufacturing to ensure robust operating procedures</li><li>Partners with Strategic Sourcing/Procurement to define technical requirements for raw materials, components, equipment, and services, ensuring on-time vendor delivery</li><li>Works with DP MSAT management to define organizational structure, prioritize strategic initiatives, and assess staffing needs to support growth</li><li>Leverages subject matter expertise to resolve emerging issues and escalates to line management as needed to manage impact</li><li>Bring demonstrated technical knowledge in drug product manufacturing, product development, and validation, along with experience interacting with Contract Manufacturing Organizations</li><li>Apply strong knowledge of industry practices and regulations (cGMP, Annex I) across multiple health authorities, including FDA, EMA, and MHRA</li></ul><p><strong>This role requires: </strong></p><ul><li>BS/BA in Engineering, Chemical Engineering, Biomedical Engineering preferred<ul><li>Principal MSAT Engineer: 8+ years of relevant experience</li><li>Staff MSAT Engineer: 10+ years of relevant experience</li></ul></li><li>Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 15:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quality Assurance Validation Specialist (Oversight)]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49486]]></requisitionid>
    <referencenumber><![CDATA[R49486]]></referencenumber>
    <apijobid><![CDATA[r49486]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49486/senior-quality-assurance-validation-specialist-oversight/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Sr. QA Validation Specialist, you will support validation of equipment, utilities, software, cleaning and sterilization processes at our facility in accordance with regulatory requirements by implementing company manufacturing standard policies and procedures. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Generates, executes and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria</li><li>Analyzes the results of testing and determines the acceptability of results against pre-determined criteria</li><li>Investigation and troubleshooting problems which occur during validations and determines solutions or recommendation for changes and/or improvements</li><li>Coordinates with functional department to resolve issues from validations</li><li>Reviews, edits and approves deviation notifications, deviation investigations and corrective actions</li><li>Coordinates with other departments or outside contractors/vendors to complete validation tasks</li><li>Develop tracking mechanism of validation activity completion for various projects and prepare status report</li><li>Present validation project and program status reports to senior management on a routine basis</li><li>Ensures that validation status is maintained for equipment and software use in commercial and clinical manufacturing</li><li>Stays current with industry trends, regulatory requirement updates and communicating to teams</li><li>May present at both internal and external (regulatory) audits</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement <ul><li>QA Validation Specialist: 4 + years of experience</li><li>Sr. QA Validation Specialist: 6+ years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-New Brunswick, NJ]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49951]]></requisitionid>
    <referencenumber><![CDATA[R49951]]></referencenumber>
    <apijobid><![CDATA[r49951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49951/medical-specialist-i-allergyent-new-brunswick-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists, Otorhinolaryngologists (ENT) and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US</p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Allergy and Otorhinolaryngology (ENT) therapeutic areas to generate product utilization. The MS will develop strong working relationships with Allergy/ENT experts and clinicians in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: New Brunswick, NJ (Flemington, Bridgewater, Princeton, East Brunswick)</p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in Allergy/ENT/Dermatology and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41999]]></requisitionid>
    <referencenumber><![CDATA[R41999]]></referencenumber>
    <apijobid><![CDATA[r41999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41999/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team at our Menands campus with a Monday-Friday 8:00am-4:30pm shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p><strong>When & where:</strong></p><ul><li>Location: Menands, New York, United States</li><li>Work Shift: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover Your Role:</strong></p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p>This Role Requires:</p><p>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level. Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred.</p><ul><li>HVAC Technician II: AAS with 2+ years of relevant experience or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years of relevant experience or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Engineer]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49585]]></requisitionid>
    <referencenumber><![CDATA[R49585]]></referencenumber>
    <apijobid><![CDATA[r49585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49585/project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><strong>Build our future together:</strong></div><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Project Engineer </strong>to join our <strong>Project Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Designing and specifying cGMP process equipment, piping, and/or controls</p></li><li><p>Managing small projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li><li><p>Preparing process and instrument drawings and other related drawings</p></li><li><p>Developing Process Flow Diagrams for manufacturing processes.</p></li><li><p>Supporting the validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Assisting in investigations of process equipment and control system anomalies</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations for and executes modification change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>Problem-solving and continuous improvement skills</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>To be considered for this opportunity you should have a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Strategic Operations & Organizational Effectiveness]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46128]]></requisitionid>
    <referencenumber><![CDATA[R46128]]></referencenumber>
    <apijobid><![CDATA[r46128]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46128/director-strategic-operations-organizational-effectiveness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Strategic Operations & Organizational Effectiveness to join our IOPS Project Management team, leading the enterprise operating system for strategy across our Industrial Operations and Product Supply organization. In this role, you will drive clarity, alignment, and cohesive execution — translating organizational priorities into actionable objectives and reinforcing them through planning, communication, and performance management — while partnering with senior leadership, HRBPs, and cross-functional teams to build the capabilities that power our long-term strategy. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United Staes</li><li>Work model: Monday - Friday 8am - 4:30pm</li><li>Travel percentage: 10% to Ireland</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead annual and quarterly strategic planning and alignment processes; align senior leadership on long-term priorities and enterprise objectives; maintain strategy artifacts including goals, cascaded objectives, roles, decision rights, and ways of working</li><li>Establish and manage the enterprise operating rhythm — planning cycles, business reviews, and strategic forums — ensuring evidence-based decisions and consistent follow-through across the organization</li><li>Define enterprise KPIs and performance indicators; integrate resourcing and capacity into prioritization; maintain scorecards and synthesize performance trends and variance analysis into actionable leadership insights</li><li>Coordinate executive reviews and strategic forums; craft clear strategy narratives and communication materials that sustain organization-wide understanding of priorities and direction</li><li>Scan external trends and translate signals into strategic implications and internal actions; identify organizational capability gaps and partner with L&LD, Tech Training, and HRBPs to build skills aligned to strategy</li><li>Develop and maintain knowledge management frameworks, repositories, playbooks, and insight archives; leverage employee engagement and sentiment data to inform strategic alignment and change readiness efforts</li><li>Produce executive presentations, visual narratives, and alignment tools that communicate complex strategy clearly and compellingly to diverse audiences</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Business Administration, Engineering, Organizational Leadership, or a related field; Master's degree (MBA or Organizational Leadership) preferred</li><li>12+ years of relevant experience in strategy, enterprise operating model design, or organizational effectiveness; level determined based on qualifications</li><li>Demonstrated experience designing and running enterprise planning and review rhythms, cross-functional alignment processes, and operating model frameworks</li><li>Proven ability to influence and facilitate across diverse senior leaders; exceptional executive communication and presentation skills</li><li>Experience with KPIs, dashboards, and scorecards; strong data fluency with the ability to translate performance insights into strategic action</li><li>Background in organizational capability building and change management — shifting mindsets, skillsets, and behaviors at scale — preferred</li><li>Experience in a global, complex, matrixed organization required; manufacturing, operations, or life sciences industry experience a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst  – Therapeutic Focus Areas]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49040]]></requisitionid>
    <referencenumber><![CDATA[R49040]]></referencenumber>
    <apijobid><![CDATA[r49040]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49040/principal-business-analyst-therapeutic-focus-areas/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Principal Business Analyst Therapeutic Focus Areas, will work collaboratively with Research & Preclinical Development scientists, as well as other IT stakeholders, to understand and document scientific lab and data processes, and translate these into requirements for the development of data and technology solutions that support Regeneron’s scientific mission.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><p>As a Principal Business Analyst, a typical day might include the following:</p><ul><li><p>Translate business strategies, goals, and objectives into clear requirements; document problem statements with quantifiable business value</p></li><li><p>Document “as is” and “to be” business processes; identify, verify, and document functional and non-functional requirements using standard methodologies and tools</p></li><li><p>Map information system connections and data flows between systems; identify data elements and provide data mapping and data dictionaries</p></li><li><p>Write SQL statements to investigate data; understand data lake principles and different database types</p></li><li><p>Maintain and prioritize the backlog of requests; ensure the development team has absolute clarity on requirements; manage business stakeholder expectations</p></li><li><p>Work with scientists and laboratory personnel to understand business processes and suggest improvements; partner with research scientists and technical teams to define system goals and requirements</p></li><li><p>Pursue data quality issues to root cause; collaborate with business and IT partners to address issues intelligently</p></li><li><p>Handle a variety of tasks, effectively solve problems with complex variables, and shift priorities as needed in a fast-paced research environment</p></li></ul><p><strong>This role requires: </strong> </p><ul><li><p> Master’s degree in a life science with experience in computer science or information technology</p></li><li><p>8+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment.</p></li><li><p>Previous experience with biological laboratory techniques, bioinformatics methods, relational database concepts, IT project and software development lifecycle methodologies, and managing or leading software development projects is preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Digital & Technology - Law, Security, Compliance, Investor Relations]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50009]]></requisitionid>
    <referencenumber><![CDATA[R50009]]></referencenumber>
    <apijobid><![CDATA[r50009]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50009/executive-director-digital-technology-law-security-compliance-investor-relations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is a leading biotechnology company built on a simple but powerful mission: to use the power of science to bring new medicines to patients, over and over again. Founded and led by physician-scientists, we've turned that mission into one of the industry's most productive pipelines, nearly all of it homegrown in our own laboratories, powered by proprietary technologies like our VelociSuite® platform. From Dupixent and EYLEA to a rapidly expanding portfolio across oncology, cardiovascular and metabolic disease, neuroscience, and rare disease, our science is reaching millions of patients worldwide, and we're just getting started.</p><p>As we invest billions in new manufacturing capacity, expand our global footprint, and build the next generation of digital and technology capabilities to match the scale of our ambition, Regeneron offers a rare combination: the resources and reach of an industry leader, paired with the energy, curiosity, and relentless focus on invention of a company still writing its next chapter. This is a place where technology doesn't just support the business, it accelerates the science that changes patients' lives.</p><p><strong>Role Description</strong></p><p>Regeneron is seeking an Executive Director to lead the digital and technology portfolio for Law, Security, and Compliance, while also holding cross-portfolio accountability for critical operating disciplines across the broader G&A and Commercial Digital and Technology portfolio. This leader will partner with senior management to shape technology strategy, strengthen portfolio governance, and ensure disciplined execution across mission-critical capabilities, including SDLC quality and audit preparedness, business-facing communications, and value realization. Decisions carry enterprise-wide, measurable long-term impact, requiring a leader who can translate business priorities into scalable, secure, compliant, and outcome-driven digital capabilities.</p><p><strong>What You'll Lead</strong></p><ul><li>Define and execute the multi-year technology strategy and transformation roadmap for Legal, Security, Compliance, and Investor Relations, aligning with corporate objectives and regulatory requirements.</li><li>Lead and optimize technology platforms supporting legal operations, contract lifecycle management, governance, risk, compliance, privacy, investigations, and corporate security.</li><li>Build and lead a high-performing technology organization, developing talent and delivery capabilities across complex enterprise functions.</li><li>Drive business outcomes through improved contract management, compliance monitoring, investigations, security operations, automation, system reliability, and user productivity.</li><li>Modernize and streamline the application landscape through enhanced integrations, workflow simplification, analytics, reporting, and scalable enterprise solutions.</li><li>Advance AI and automation strategies, including responsible AI governance, to improve decision-making, operational efficiency, risk management, and controls effectiveness.</li><li>Standardize global processes and operating models across legal, compliance, privacy, security, and related shared services functions.</li><li>Oversee vendor management, technology investments, audit readiness, cybersecurity, business continuity, communications, and portfolio governance to ensure secure, compliant, and high-value service delivery.</li></ul><p><strong>What You Bring</strong></p><ul><li>BS/BA in Computer Science, Information Systems, Business, or a related field required; MS, JD or MBA preferred.</li><li>17+ years of progressive technology leadership, including teams supporting law, security, compliance, risk, governance, or other highly regulated enterprise functions.</li><li>Strong command of legal, security, compliance, GRC, privacy, investigations, contracts, investor relations, and enterprise workflow platforms, with the judgment to stay platform-agnostic.</li><li>Experience with enterprise platforms supporting Law, Security, Compliance, GRC, privacy, legal operations, contracts, investigations, service management, and analytics is preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp QC Analyst - Bioassay]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48429]]></requisitionid>
    <referencenumber><![CDATA[R48429]]></referencenumber>
    <apijobid><![CDATA[r48429]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48429/temp-qc-analyst-bioassay/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temporary QC Analyst - Bioassay </strong>to join our <strong>QC Biology and Biochemistry </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick.</li><li>12 Month contract position.</li></ul><div><div><div><div><div><div><div><div><div><p><strong>What you’ll do:</strong></p><ul><li><p>Conducting tests on, in-process, release, stability, and/or research samples.</p></li><li><p>Gathering data and documents test results for techniques such as cell-based potency and ELISA for Bioassay.</p></li><li><p>Performing cell biology techniques such as mammalian cell culture, preparing reagent aliquots and media for use in cell-based assays.</p></li><li><p>Reviewing test results to ensure compliance with standards; reports any quality anomalies.</p></li><li><p>Complying with all pertinent regulatory agency requirements.</p></li><li><p>Conducting testing on in-process, product, stability, and/or research samples.</p></li><li><p>Writing and revising control test procedures and SOPs.</p></li><li><p>Completing test records and reviews data.</p></li><li><p>Calibrating or verifying calibration of instruments/devices prior to use.</p></li><li><p>May assist in validation of methods.</p></li><li><p>Involved in establishing the transfer of methodology from R&D.</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Strong attention to detail, excellent written and oral communication skills.</p></li><li><p>Ability to prioritise, manage multiple tasks, and meet deadlines.</p></li><li><p>Ability to organise and maintain data or information.</p></li><li><p>Ability to learn through observation and hands on experience.</p></li><li><p>Preferably experience with molecular biology and cell biology techniques such as ELISA, Bioassay and mammalian cell culture.</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Requires BS/BA in Life Sciences or related field; will substitute relevant experience for education.</p></li><li><p>Experience with electronic systems such as LIMS, ViCell, SoftMax, Hamilton Venus, Labware is an advantage.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLQC</p></div></div></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - ALBANY, NY]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48003]]></requisitionid>
    <referencenumber><![CDATA[R48003]]></referencenumber>
    <apijobid><![CDATA[r48003]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48003/medical-account-specialist-ii-neurology-albany-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Albany]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Albany (Metro), NY</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div></div><div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - BOSTON, MA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48001]]></requisitionid>
    <referencenumber><![CDATA[R48001]]></referencenumber>
    <apijobid><![CDATA[r48001]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48001/medical-account-specialist-ii-neurology-boston-ma/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Boston]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Boston (Metro), MA</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div></div><div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p><p><br> </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -SAN FRANCISCO, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48076]]></requisitionid>
    <referencenumber><![CDATA[R48076]]></referencenumber>
    <apijobid><![CDATA[r48076]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48076/medical-account-specialist-ii-neurology-san-francisco-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Francisco]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: San Francisco (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CLEVELAND, OH]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48006]]></requisitionid>
    <referencenumber><![CDATA[R48006]]></referencenumber>
    <apijobid><![CDATA[r48006]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48006/medical-account-specialist-ii-neurology-cleveland-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cleveland]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Cleveland (Metro), OH</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - SAN ANTONIO, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48065]]></requisitionid>
    <referencenumber><![CDATA[R48065]]></referencenumber>
    <apijobid><![CDATA[r48065]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48065/medical-account-specialist-ii-neurology-san-antonio-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Antonio]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: San Antoinio (Metro), TX</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NEWARK, NJ]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48011]]></requisitionid>
    <referencenumber><![CDATA[R48011]]></referencenumber>
    <apijobid><![CDATA[r48011]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48011/medical-account-specialist-ii-neurology-newark-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Newark]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Newark (Metro), New Jersey</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager - Delivery & Operations Product Lead – Authoring Platform]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47587]]></requisitionid>
    <referencenumber><![CDATA[R47587]]></referencenumber>
    <apijobid><![CDATA[r47587]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47587/senior-product-manager-delivery-operations-product-lead-authoring-platform/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Global Development IT is seeking a strategic, hands-on Senior Product Manager to serve as Product Lead for Regeneron’s enterprise generative-AI document-authoring platform. You will be responsible for a multi-phase implementation that delivers governed, scalable AI capabilities across Clinical, Regulatory, Medical Affairs, Labeling, and other Global Development domains. Partnering with business and technology stakeholders, you will align platform strategy to scientific, regulatory, and operational needs, ensuring secure, compliant, and high-impact outcomes.</p><p>Reporting to the Associate Director, Product Management of Enabling Technologies, you will drive the full product lifecycle—from vision and roadmap through design, build, validation, launch, and optimization. Your blend of clinical-process know-how, agile product leadership, and deep AI expertise will accelerate content creation, improve quality, and reduce cycle times for regulated documents.</p><p><strong>In this role, a typical day might include the following:</strong> <br>- Leading stand-ups, refining backlogs, and approving user stories for AI-powered authoring features <br>- Facilitating workshops with Clinical, Regulatory, and Medical Affairs teams to gather requirements and prioritize enhancements <br>- Reviewing solution architecture to enforce security, privacy, and GxP compliance across RAG, MCP, LLM, Copilot, and Claude integrations <br>- Tracking sprint progress, surfacing risks, and updating program leadership on scope, budget, and return of investment<br>- Defining guardrails for citizen development and coordinating change-control / governance forums <br>- Monitoring platform adoption and performance to identify automation and continuous-improvement opportunities</p><p><strong>This job might be for you if you: </strong> <br>- Translate sophisticated Global Development document workflows into intuitive, AI-enabled products <br>- Excel at influencing cross-functional teams without direct authority and communicating clearly with executive stakeholders <br>- Thrive in agile environments, balancing tactical delivery with long-term platform strategy <br>- Enjoy partnering with data-science teams to embed generative AI into regulated processes <br>- Keep current on industry standard processes and proactively incorporate them into product roadmaps <br>- Maintain a “get-it-done” attitude and balance multiple high-priority initiatives simultaneously</p><p><strong>In order to be considered for this role, you must have: </strong><br>- BS/BA with 8–10 years validated experience (or MS/MBA with 6+ years as an equivalent), including 3 years in enterprise SaaS and 1+ year delivering generative/agentic-AI solutions <br>- Shown success leading end-to-end GxP implementations of AI document-authoring platforms, using agile/DevOps methods <br>- Validated expertise in RAG, MCP, LLMs, Copilot, Claude, and integration across Clinical, Regulatory, and Medical Affairs systems</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Market Access Director Oncology]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48536]]></requisitionid>
    <referencenumber><![CDATA[R48536]]></referencenumber>
    <apijobid><![CDATA[r48536]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48536/market-access-director-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director Market Access Oncology International to join our market access team, supporting our international oncology business in a hybrid work model. In this role, you will lead the development and execution of market access, pricing, and reimbursement strategies for an oncology portfolio while collaborating with commercial, health economics and outcomes research, medical affairs, clinical, marketing, and affiliate teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>Madrid - Spain<br>Hybrid</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead market access strategy and execution to enable successful in-country oncology launches, including value propositions, objection handlers, and launch readiness activities</p></li><li><p>Develop and implement pricing and reimbursement strategies across market archetypes to achieve optimal patient access and value</p></li><li><p>Synthesize payer insights and analyse market access environment trends, including competitor dynamics, to inform strategic decisions</p></li><li><p>Guide affiliates in preparing reimbursement dossiers and managing payer negotiations within defined price corridors to ensure timely access</p></li><li><p>Deliver recommendations on payer strategy, evidence generation, data collection, and value demonstration aligned to access objectives</p></li><li><p>Coordinate cross-functional input to address payer requirements throughout reimbursement processes and inform global pricing decisions</p></li><li><p>Develop annual tactical plans, manage project budgets and vendors, and maintain reimbursement tracking tools to monitor execution</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree with a minimum 10 years of in-country market access experience or global commercial strategy experience</p></li><li><p>Minimum 7 years of in-country oncology market access experience preferred</p></li><li><p>Proven experience supporting or leading product launch activities in a market access context</p></li><li><p>Experience developing pricing and reimbursement strategies and supporting payer negotiations and dossiers</p></li><li><p>Ability to integrate payer evidence needs into clinical development programs and identify evidence gaps</p></li><li><p>Strong project and process management skills with the ability to manage multiple priorities</p></li><li><p>Experience leading cross-functional or matrix teams</p></li><li><p>Demonstrated ability to build effective relationships with internal stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€96,000.00 - €160,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Commercial Solutions]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48998]]></requisitionid>
    <referencenumber><![CDATA[R48998]]></referencenumber>
    <apijobid><![CDATA[r48998]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48998/director-commercial-solutions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Commercial Solutions to join our Global Commercial Digital & Technology organization. In this leadership role, you will be responsible for building and scaling commercial technology capabilities within our Global Capability Center while serving as a strategic partner to global business and technology leaders. You will lead the delivery of innovative technology, data, and AI-enabled solutions that support commercial operations, customer engagement, analytics, market access, and patient services. This role offers a unique opportunity to shape the future of commercial digital transformation by combining deep commercial domain expertise, technology leadership, and organizational development within a highly collaborative global environment.</p><p>When & Where:</p><p><strong>Hyderabad,</strong> <strong>India</strong> <strong>(Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Lead and scale the Commercial Digital & Technology organization within the Global Capability Center, fostering a high-performance, inclusive, and innovation culture.</p></li><li><p>Build and expand commercial technology capabilities through hiring, onboarding, talent development, and organizational design.</p></li><li><p>Partner with global commercial and technology leaders to define and implement business-aligned technology strategies that support commercial growth objectives.</p></li><li><p>Lead end-to-end technology, architecture, data, and solution delivery across Agile and traditional delivery models.</p></li><li><p>Deliver and optimize commercial technology platforms including CRM, customer engagement, commercial analytics, data management, incentive compensation, and omnichannel solutions.</p></li><li><p>Establish operational excellence through delivery governance, performance metrics, process improvement, and continuous optimization.</p></li><li><p>Ensure compliance with applicable healthcare regulations, data privacy requirements, commercial governance frameworks, and audit readiness standards.</p></li><li><p>Drive adoption of AI and Generative AI capabilities by identifying practical business use cases while ensuring compliance in regulated commercial environments.</p></li><li><p>Act as a strategic advisor to senior stakeholders by translating complex business challenges into scalable and actionable technology solutions.</p></li><li><p>Communicate effectively with executive leadership and cross-functional teams across global regions, driving alignment and informed decision-making.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Information Technology, Engineering, Business, Life Sciences, or a related field; advanced degree preferred.</p></li><li><p>Significant leadership experience in pharmaceutical, biotechnology, healthcare, or other highly regulated industries.</p></li><li><p>Deep knowledge of pharmaceutical and biotechnology commercial operations, including Sales, Marketing, Omnichannel Engagement, Market Access, Commercial Analytics, Commercial Operations, and Patient Services.</p></li><li><p>Experience leading large-scale technology organizations and global delivery teams across architecture, engineering, and data rigors.</p></li><li><p>Strong understanding of commercial technology ecosystems including Veeva CRM, Salesforce platforms, Data Cloud, Marketing Cloud, master data management, commercial analytics, and customer engagement solutions.</p></li><li><p>Knowledge of healthcare industry regulations including GDPR, HIPAA, consent management, transparency requirements, and commercial compliance standards.</p></li><li><p>Experience establishing and expanding Global Capability Center (GCC) organizations or similar global operating models.</p></li><li><p>Demonstrated experience evaluating, implementing, and governing AI and Generative AI solutions that deliver measurable business value.</p></li><li><p>Proven ability to influence senior collaborators and operate effectively within complex global matrix environments.</p></li><li><p>Strong critical thinking, problem-solving, organizational leadership, and executive communication skills.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Nürnberg - Regensburg - Coburg - Hof]]></title>
    <date><![CDATA[Sun, 12 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49154]]></requisitionid>
    <referencenumber><![CDATA[R49154]]></referencenumber>
    <apijobid><![CDATA[r49154]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49154/sales-specialist-immunology-fmd-nuernberg-regensburg-coburg-hof/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Respiratory division at key meetings. You will identify the key people in Pneumology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><p><br></p><p><strong>Where:</strong></p><p><br></p><p>Field based in the territory: <strong>Nürnberg - Regensburg - Coburg - Hof</strong></p><p><br></p><p><strong>Discover your role:</strong></p><p><br></p><ul><li>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</li><li>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</li><li>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</li><li>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</li><li>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</li><li>Regular reporting to the sales management</li></ul><br><p><br></p><p><strong>This role requires:</strong></p><p><br></p><ul><li>Deep understanding of the local healthcare economy, with the ability to identify key players in Pneumology</li><li>“Patient first” value system</li><li>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech/pharmaceutical sector</li><li>Respiratory experience is preferred</li><li>Proficiency in German as well as conversational English</li><li>Readiness for very frequent travel and a driver's license cl. 3/B.</li></ul><p><br><br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Warehouse Associate]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49117]]></requisitionid>
    <referencenumber><![CDATA[R49117]]></referencenumber>
    <apijobid><![CDATA[r49117]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49117/lead-warehouse-associate/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Lead Warehouse Associate </strong>to join our <strong>Warehouse and Logistics </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: 24/7</li><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Unloading trucks, lifting heavy items, and operating a forklift.</li><li>Unpacking and checking goods received against purchase orders or invoices. Maintaining paper and/or electronic records of received goods.</li><li>Transferring materials physically to QA Release Area, appropriate storage location, or process area and documenting the transfers in computerised systems.</li><li>Preparing and maintaining paper and electronic records of materials received. Confirming the accuracy of inventory receipts as per the packing slip and/or Certificate of Analysis.</li><li>Examining, stocking, and distributing materials in inventory and to manufacturing.</li><li>Scheduling deliveries of incoming raw materials.</li><li>Packing out materials being shipped as per SOP’s Loads Trucks for shipment</li><li>Assisting with shipping of finished products for filling, labeling and distribution.</li><li>Assisting with receipt of finished product from fillers, labelers and any other source.</li><li>May participate in the Supplier Corrective Action Request (SCAR) program.</li><li>Participating in NOE’s, EOE’s, or CAPA’s as required.</li><li>Monitoring employees training to ensure that all requirements are met, including OJT.</li><li>Perform monthly performance feedback meetings with direct reports.</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Ability to think creatively, proactively and propose solutions with attention to detail.</li><li>Ability to effectively communicate issues and ideas with peers and with management.</li><li>Ability to build effective working relationships throughout the organisation.</li><li>Ability to operate independently while maintaining deadlines.</li><li>Self-starter with a resilient, can-do attitude.</li><li>Ability to adapt to a quickly changing environment.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Requires a HS Diploma/GED/Leaving Cert or equivalent, plus one year relevant experience.</li><li>Associate’s degree and/or warehouse experience preferred.</li><li>Experience in a cGMP environment preferred.</li><li>Experience operating a forklift, handheld scanner and or CDL is a plus.</li></ul><h3>Thrive today. Grow tomorrow.</h3><h3>#IRELIM #JOBSIEST #LI-Onsite</h3><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€18.54 - €28.99]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Information Technology Program Manager - Velocigene]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48890]]></requisitionid>
    <referencenumber><![CDATA[R48890]]></referencenumber>
    <apijobid><![CDATA[r48890]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48890/information-technology-program-manager-velocigene/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Information Technology Program Manager Velocigene will work collaboratively with business stakeholders in multiple scientific areas involved in our Genetically Modified Animal Pipeline to perform robust project and portfolio planning, and then execute upon that plan to completion; aligning to the project management triple constraint of scope, time and cost. We see this position as critical to executing IT projects for Regeneron and specifically, Velocigene . The candidate must have excellent time management skills to function in a fast-paced environment, demonstrating independent work skills, strong work ethic, and a passion for helping to fuel the Research IT pipeline. The candidate will be responsible for coordinating project activities from ideation through transition to the run team. The ideal candidate will have notable experience in planning, monitoring and closing projects, and coordinating multiple workstreams. We hope you are excited by this opportunity to transform Regeneron’s approach to IT project management and execution.</p><p><strong> </strong></p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Responsible for activities of a highly complex nature, which may include small projects or large programs involving multiple project workstreams, and act as a single point of contact for those activities</p></li><li><p>Actively manage large projects directly with varying degrees of complexity, and coordinate multiple project streams with inter-dependencies</p></li><li><p>Utilizing agile methodologies such as Scaled Agile Framework (SAFe)</p></li><li><p>Recommend and take action to direct the analysis and solution of problems</p></li><li><p>Communicate with stakeholders on an ongoing basis; estimate resources and participants needed to achieve project goals; draft and submit budget proposals and recommend subsequent budget changes where necessary; manage multiple projects as necessary</p></li><li><p>Plan and schedule project timelines and milestones using appropriate tools; track project milestones and deliverables; develop and deliver progress reports, proposals, requirements documentation and presentations</p></li><li><p>Acting as the go-to-person and single point of contact for status and plans involving complex and inter-dependent program</p></li><li><p>Coordinate with IT and department managers to assess and track plans, status, etc. for on-time delivery of critical projects and programs; this includes assisting teams and the project teams in removing impediments and resolving cross-team issues</p></li><li><p>Ability to define the project objectives clearly and rally a team around the value delivery plan</p></li><li><p>Ensure teams keep a laser focus on what needs to be completed, and when, to keep programs on track</p></li><li><p>Looking ahead anticipating risks before they are issues</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Bachelor’s degree in a life science with experience in computer science or information technology.</p></li><li><p>7+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment.</p></li><li><p>Someone adept at using a variety of technologies (Planview, Jira, MS tools, etc.) and processes (SDLC, PMO, etc.) Previous project management in a Research organization is preferred. Must be open to travel periodically (~5%) to represent Regeneron as needed and for internal meetings.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Information Technology Program Manager, Preclinical Manufacturing and Process Development]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48966]]></requisitionid>
    <referencenumber><![CDATA[R48966]]></referencenumber>
    <apijobid><![CDATA[r48966]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48966/information-technology-program-manager-preclinical-manufacturing-and-process-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we are looking for an outstanding Program Manager to implement IT projects for Preclinical Manufacturing & Process Development (PMPD). This role will work with PMPD stakeholders to perform robust project planning and execute upon that plan to completion, aligning to the project management of scope, time and cost.</p><p><strong>When & where:</strong> This role is based at Tarrytown, NY location with a minimum of 4+ days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead large-scale projects with varying degrees of complexity </p></li><li><p>Lead small projects involving multiple project workstreams, acting as a single point of contact for those activities </p></li><li><p>Utilize agile methodologies such as Scaled Agile Framework (SAFe) </p></li><li><p>Recommend and take action to direct the analysis and solution of problems </p></li><li><p>Communicate with stakeholders on an ongoing basis; estimate resources and participants needed to achieve project goals; draft and submit budget proposals and recommend subsequent budget changes where necessary; handle multiple projects as necessary </p></li><li><p>Plan and schedule project timelines and milestones using appropriate tools; track project milestones and deliverables; develop and deliver progress reports, proposals, requirements documentation and presentations </p></li><li><p>Act as the go-to-person and single point of contact for a specific process, product, function or system </p></li><li><p>Coordinate with IT and department managers to assess and track plans, status, etc. for timely delivery of critical projects and programs; this includes assisting teams and the project teams in removing impediments and resolving cross-team issues </p></li><li><p>Responsible for defining project objectives clearly and rally a team around the value delivery plan </p></li><li><p>Anticipating risks before they become issues </p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>A bachelor's degree</p></li><li><p>Proven work experience in research, pharmaceutical, biotechnology, or scientific laboratory environment implementing IT systems </p></li><li><p>Expert user of a variety of technologies (Planview, Jira, MS tools, etc.) and processes (SDLC, PMO, etc.)</p></li><li><p>Must be open to travel periodically (~5%) to represent Regeneron as needed and for internal meetings</p></li><li><p>Previous project management in a Research organization is preferred. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Strategy & Operations, Genetic Medicines]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48279]]></requisitionid>
    <referencenumber><![CDATA[R48279]]></referencenumber>
    <apijobid><![CDATA[r48279]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48279/associate-director-strategy-operations-genetic-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Regeneron Genetic Medicines Clinical Development Unit (RGM CDU). The Associate Director Strategy Planning & Operations reports to and works closely with the RGM CDU Leadership Team (LT) in support of the operational management of the department. The scope of this role includes supporting departmental meetings, objective and goal setting, support of cross-functional projects, review and tracking of RGM CDU top deliverables, headcount and resource forecasting, and team communications. The role also supports initiatives to establish a high-performing, strategic, effective, and quality-focused organization that is well-aligned and integrated with other functions, including RGM research, the Regeneron Genetic Center (RGC), and Global Development. A key expectation of this role is the active adoption and promotion of AI-powered productivity tools to elevate quality, speed, and impact of strategic work across the organization.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Tarrytown, NY</p><p><strong>Discover your role:</strong></p><ul><li><p>Act as a strategic partner across the RGM CDU Leadership Team (LT) and the broader organization, driving alignment in support of portfolio and departmental planning with an emphasis on long-term strategic objectives.</p></li><li><p>Provide comprehensive support to the LT including:</p></li><li><p>Overseeing the collation and tracking of critical program and departmental initiatives, ensuring alignment with organizational goals.</p></li><li><p>Leading cross-functional strategic initiatives, special projects, and organizational planning efforts to foster collaboration and innovation.</p></li><li><p>Developing and delivering high-impact presentations for the Head of the RGM CDU, covering key departmental topics such as pipeline progress, strategic issues, RGM overviews for external collaborators, financial performance updates, and organizational changes</p></li><li><p>Enhancing resource management strategies</p></li><li><p>Strategic mid-range planning for headcount needs, encompassing both permanent and contract staff, while proactively managing the approval process for permanent headcount</p></li><li><p>Guiding RGM line managers in performance and talent management discussions, while partnering with functional leaders to refine succession planning processes</p></li><li><p>Spearhead infrastructure and space planning initiatives, developing strategic recommendations for changes in collaboration with the RGM CDU LT to optimize operational efficiency</p></li><li><p>Lead the preparation and facilitation of monthly departmental meetings, including strategic planning, communications, agenda development, and comprehensive minutes' distribution to ensure accountability and follow-up on key action items</p></li><li><p>Identify and champion opportunities for continuous improvement, proposing innovative solutions to enhance operational efficiencies through regular engagement with RGM CDU & ES LT and their teams</p></li><li><p>Collaborate extensively with other Global Development Strategic Planning & Operations personnel to navigate process changes and address issues impacting RGM CDU and Global Development, ensuring alignment with broader organizational strategies</p></li><li><p>Champion the adoption of AI productivity tools (e.g. Claude, Microsoft Pilot) across RGM CDU to streamline operational workflows, accelerate document and presentation development, synthesize complex information, and enhance strategic output</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and 10+ years experience required; (e.g. MBA, PhD, Pharm D) preferred</p></li><li><p>Demonstrated depth of understanding of the drug development process</p></li><li><p>This role is both strategic and tactical and requires an agile problem solver with strong planning ability, interpersonal and communication skills, along with scientific and business acumen to work across the RGM CDU and with our partners to advance strategic planning and team communication</p></li><li><p>Demonstrated proficiency in AI-powered productivity tools (e.g., Claude, Microsoft Copilot, or equivalent) with a track record of applying them to accelerate knowledge work — including drafting, research synthesis, structured analysis, and presentation development</p></li><li><p>Comfort operating at the frontier of AI tool adoption, with curiosity and initiative to identify new applications, evaluate emerging tools, and guide others in their use</p></li><li><p>Demonstrated ability to prioritize and manage multiple projects simultaneously; Experience in contributing or leading cross-functional strategic change initiatives</p></li><li><p>Expertise in MS applications including (but not limited to) TEAMS, Project, PowerPoint, Word, Excel</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48188]]></requisitionid>
    <referencenumber><![CDATA[R48188]]></referencenumber>
    <apijobid><![CDATA[r48188]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48188/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br><br>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.<br><br><strong>When & where:</strong><br><br>Work Location: Uxbridge, UK</p><p><br>25% Travel may be required<br><br><br><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective action</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Finance Operations Associate Manager]]></title>
    <date><![CDATA[Sun, 26 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48492]]></requisitionid>
    <referencenumber><![CDATA[R48492]]></referencenumber>
    <apijobid><![CDATA[r48492]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48492/temporary-finance-operations-associate-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Associate Manager, Finance Operations Accounting to join our Finance Operations Team, supporting our Dublin in a hybrid work mode. In this role, you will ensure accuracy in financial data, optimize accounting workflows, and manage a team of professionals to support key financial goals while collaborating with cross-functional teams, Accounting leadership, and offshore teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. This is a temporary 6 month contract.</p><h3>When & where:</h3><p>Dublin — hybrid</p><h3>Discover your role:</h3><ul><li><p>Lead cross-functional initiatives to improve and automate accounting processes</p></li><li><p>Develop process models and workflow diagrams to support decision-making</p></li><li><p>Manage and support a team delivering accounting analysis and insights</p></li><li><p>Track performance metrics to identify improvements and support financial goals</p></li><li><p>Deliver reports, dashboards, and presentations to Accounting leadership</p></li><li><p>Partner with offshore teams to ensure timely accounting close deliverables</p></li><li><p>You collaborate effectively across teams in a global organisation</p></li><li><p>You manage competing priorities and drive results across multiple projects</p></li></ul><h3>This role requires:</h3><ul><li><p>Bachelor’s degree in Accounting and 6–8+ years’ accounting experience</p></li><li><p>Strong understanding of Sarbanes-Oxley (SOX) controls</p></li><li><p>Expertise in business process design and documentation</p></li><li><p>Experience working in a global multinational accounting environment</p></li><li><p>Knowledge of large-scale Enterprise Resource Planning systems preferred</p></li><li><p>Six Sigma certification preferred</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I - Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47874]]></requisitionid>
    <referencenumber><![CDATA[R47874]]></referencenumber>
    <apijobid><![CDATA[r47874]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47874/process-development-engineer-i-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer I</strong> to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) group, part of our Preclinical Manufacturing & Process Development (PMPD) department. In this exciting new role, you will develop manufacturing processes for the production of synthetic small molecules used in Regeneron's diverse range of therapeutic modalities, working in close collaboration with cross-functional teams to perform chemical process development and optimization using Quality by Design (QbD) principles for GMP production.</p><p>This position offers the opportunity to contribute to process scale-up and technology transfer of manufacturing workflows to Contract Development and Manufacturing Organizations (CDMOs), helping ensure timely and reliable entrance to the clinic and eventual commercialization.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours, with on-site presence during scale-up/GMP manufacturing activities as needed</li><li>Location: On-site laboratory setting</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support lab operations, with occasional travel to CDMO sites for technology transfer</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Work at the bench to design and develop scalable, robust, and controlled GMP-ready processes for synthetic small molecules</li><li>Collaborate with analytical groups within or outside the organization to establish supportive analytical characterization of synthetic intermediates and final products</li><li>Discuss plans and data in multi-functional teams to evaluate processes and determine developmental goals, ensuring integrated program success</li><li>Use statistical design of experiments (DOE) to optimize synthetic chemical processes, including reaction parameters, purification operations, and analytical characterization</li><li>Partner with the External Manufacturing group and other key partners at Regeneron's IOPS organization to provide technical assessment of CDMOs intended for GMP production and successfully transfer processes with immediate, first-time success</li><li>Research, identify, and develop new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT)</li><li>Author robust technology transfer documentation and support production with onsite presence during scale-up/GMP manufacturing activities</li><li>Analyze and present data in a clear and cohesive manner to a broad audience, facilitating data-driven decision-making</li><li>Author, review, or provide domain expertise for publications, reports, tech transfer documents, regulatory support documents, and patents</li><li>Coach and mentor junior team members of the organization as needed</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is a hands-on, on-site laboratory role requiring bench work to design and develop synthetic small-molecule processes, along with proactive compliance with lab safety and environmental safety expectations set by Regeneron and regulatory bodies such as the FDA and DoT.</li><li>Flexibility to multitask and work both independently and within cross-functional teams, along with occasional onsite presence during scale-up/GMP manufacturing activities, is required.</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><h3>Must-haves:</h3><ul><li>Bachelor's degree with 4 years of relevant experience, or Master's degree with 0-3 years of relevant experience, in active pharmaceutical ingredient (API) process development</li><li>Strong initiative and drive to complete challenging tasks and learn new technologies</li><li>Strong fundamental understanding of process chemistry and technology transfer principles</li><li>Excellent interpersonal, verbal, and written communication skills, with the ability to think critically and demonstrate problem-solving skills</li><li>Well-versed with purification techniques such as crystallization, extraction, and chromatography</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Experience with small molecules in the bioconjugates space</li><li>Hands-on experience with organic molecule synthesis and characterization tools such as mass spectrometry, NMR, IR spectroscopy, and HPLC</li><li>Proven experience scaling up synthetic small-molecule reactions and technology transfer to a GMP manufacturing facility</li><li>Experience handling highly potent compounds using appropriate containment and best-practice procedures</li><li>Well-versed with ICH/regulatory guidelines and their impact on process development of synthetic molecules and bioconjugates</li><li>Experience working with cross-functional CMC teams, and experience authoring publications, reports, tech transfer documents, regulatory support documents, and patents</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Automation Systems Administrator, Manufacturing & Lab Support]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48743]]></requisitionid>
    <referencenumber><![CDATA[R48743]]></referencenumber>
    <apijobid><![CDATA[r48743]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48743/principal-automation-systems-administrator-manufacturing-lab-support/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Automation Systems Administrator to join our IOPS team, providing technical leadership in the configuration and administration of automated and computerized systems, servers, and network infrastructure across our manufacturing and laboratory operations. In this role, you will serve as the technical SME bridging Automation and the business — driving validation, continuous improvement, and strategic vendor partnerships — while collaborating with Engineering, Quality, IT, and cross-functional teams across the organization. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Menands, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Develop system hardware and software specifications, code, and networking configurations and standards to meet cGMP and procedural requirements across IOPS</li><li>Provide advanced technical automation support, troubleshooting, and investigations in accordance with established SOPs, GAMP 5 guidelines, and departmental practices</li><li>Lead system SAT/FAT, validation, qualification, and improvement efforts; manage small to large interdepartmental and global projects related to corrective action, software and hardware improvement, and new equipment or infrastructure</li><li>Initiate, author, and review Software Lifecycle Documentation, SOPs, Change Controls, EOEs, NOEs, DNFs, risk assessments, impact statements, and corrective and preventive action plans</li><li>Act as technical liaison between Automation and the business, independently identifying alternative solutions to ambiguous problems and driving continuous improvement in processes, procedures, and architecture standards</li><li>Support selection and assessment of strategic automation partners and vendors; manage vendor relationships and deliverables in alignment with regulatory and business requirements</li><li>Provide training and mentoring to Engineering, Automation, and external departments; may supervise or mentor direct reports and contractors within the department</li><li>Direct experience in a pharmaceutical or biopharmaceutical manufacturing facility preferred</li><li>Advanced experience configuring and troubleshooting control, monitoring, and product release testing systems including design and installation</li><li>Advanced experience troubleshooting network infrastructure and server-based systems</li><li>Current knowledge of cGMP biotech and pharma operations, regulatory and quality policies, procedures, and documentation methods</li><li>Strong project management capabilities with the ability to lead changing priorities and make timely decisions across multiple departments and workstreams</li></ul><h3><strong>This role requires:</strong></h3><ul><li>BS/BA in Science, Engineering, or a related field</li><li>Principal Automation Systems Administrator: 8+ years of relevant experience</li><li>Staff Automation Systems Administrator: 10+ years of relevant experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - SAN FRANCISCO, CA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48961]]></requisitionid>
    <referencenumber><![CDATA[R48961]]></referencenumber>
    <apijobid><![CDATA[r48961]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48961/medical-account-specialist-ii-hematology-san-francisco-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: San Francisco, CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Artificial Intelligence Data Engineer]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44147]]></requisitionid>
    <referencenumber><![CDATA[R44147]]></referencenumber>
    <apijobid><![CDATA[r44147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44147/senior-manager-artificial-intelligence-data-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Global Development is embarking on a Digital Transformation project incorporating AI, machine learning, and automation to help us reduce cycle times, improve quality allowing us to focus on more meaningful work. We focus on developing and improving data pipelines, infrastructure, architecture, and analytic tools to allow resources to fuel our transformation. Working with a team of engineers, analysts, and scientists, you will contribute to modernizing our clinical data infrastructure. This highly visible role will be a technical and strategic liaison between the transformation projects and IT. </p><p>A key responsibility will be developing and optimizing schema and data models for clinical data. We ensure that those products are standard compliant and interoperable with other platforms and data sources. This role will also contribute to data governance strategy and to the development and management of tools improving and monitoring data quality. The data engineer will also develop processes to automate routine workflows. The engineer will also provide technical leadership and mentorship and will stay current with innovations in data engineering so that they may be evaluated for implementation. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where: </strong>Tarrytown, NY,<strong> </strong> Armonk, NY or Warren, NJ offices. </p><p><strong>Discover your role:</strong><br>• Work with a cross-functional team to optimize and implement our data strategy with a focus on optimization for digital transformation and the use of AI/ML<br>• Design and document end-to-end data architectures that support diverse analytic, operational, and research needs.<br>• Facilitate the implementation of a modern data platform (e.g. Snowflake, Databricks, etc.)<br>• Identify opportunities and implement solutions to increase data interoperability and standardization among systems and across other business units.<br>• Develop and implement pipelines to monitor and improve both internal and external (i.e., from CRO partners) data quality.<br>• Work with informatics and AI engineers optimizing the utility of data for their respective pipelines.<br>• Monitor and optimize the performance of data architectures and platforms.<br>• Develop or implement critical metrics to measure the impact of the overall data strategy.<br>• Stay up to date with the latest advances in the field and, as appropriate, evaluate them for adoption </p><p><strong>This role requires:</strong><br>An advanced degree in computer science, statistics, biomedical informatics, or a related field is preferred (PhD + 2 years of experience or an MS + 4 years of relevant experience). A minimum of 5 years’ experience developing and leading the implementation of data engineering solutions, including accountability for the success of the implementation, in life sciences or healthcare<br>• Demonstrated expertise in designing and maintaining infrastructure and architecture for clinical or biomedical data in a healthcare or life sciences setting.<br>• Expertise in modern data platforms (e.g., Snowflake, Redshift, BigQuery, Databricks) and programming languages such as Python, SQL, R, etc.<br>• Maintain and manage code repositories (e.g Bitbucket) ensuring clean, well-documented code with proper version control.<br>• Proficiency in cloud architecture (e.g. AWS, Azure, GCP) and DevOps practices. Recognized certifications are a plus.<br>• Experience building, scaling, and maintaining pipelines for structured and unstructured data. Ability to integrate pipelines across the enterprise is essential.<br>• Deep understanding of regulatory frameworks (HIPAA, GDPR, 21 CFR Part 11) and clinical data standards (CDISC, HL7, FHIR).<br>• Knowledge of machine learning pipelines and integration with clinical data platforms.<br>• May require travel up to 20%.</p><p><br>#AAI</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - PRINCETON, NJ]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48787]]></requisitionid>
    <referencenumber><![CDATA[R48787]]></referencenumber>
    <apijobid><![CDATA[r48787]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48787/medical-account-specialist-ii-hematology-princeton-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New Jersey]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Job Description</p><p><strong>Geography: Princeton, New Jersey</strong></p><p>The Hematology Oncology Account Specialist, is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li>Engage Hematology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of two bispecific agents to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Therapeutic Area Genetics (Immunology)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46254]]></requisitionid>
    <referencenumber><![CDATA[R46254]]></referencenumber>
    <apijobid><![CDATA[r46254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46254/associate-director-therapeutic-area-genetics-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We are looking for an extremely talented Scientist to join our Immunology Therapeutic Area Genetics (TAG) team. Within the Regeneron Genetics Center, the Immunology TAG team is using large-scale human exome sequencing for discovery and validation of new therapeutic targets in autoimmune and other immune-mediated disease. You will be responsible for designing and executing studies integrating large scale human genetics and multidimensional omics datasets derived from RGC and public resources in the immunology space to identify new targets for inflammatory and auto-immune diseases and accelerate target transition to novel therapeutics. You will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to catalyze therapeutic development for genetically-validated targets in immunologic diseases.</p><div><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY</p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><ul><li><p>Understand and leverage RGC and Regeneron datasets, external resources, and the scientific/medical literature to generate research questions and then generate relevant phenotypes from longitudinal clinical data, design and execute genetic association studies, and perform integrative omics analyses to address these research questions</p></li><li><p>Deploy computational methods to integrate genetic data with multiple omics data to more effectively identify/prioritize drug targets illuminated by genetic association data.</p></li><li><p>Work closely with other members of the Immunology and other TAG teams, Analytic Genetics, Sequencing, and GIDE in cross-functional initiatives within the RGC and Regeneron.</p></li><li><p>Collaboratively summarize insights of investigations into a variety of formats (e.g. documents, presentations, patent applications, publications, etc.) for audiences with broad backgrounds.</p></li><li><p>Partner with Clinical Development to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations.</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>PhD or MD preferred with 8+ years of experience in the use of WES/GWAS datasets, RNA-Seq, proteomics and other large-scale platforms for genomic/proteomics.</p></li><li><p>Demonstrated expertise in immunobiology, genetics, and mechanisms; familiarity with large genetic studies that deliver novel genetic findings and medically relevant gene discoveries;</p></li><li><p>Demonstrated ability to manage and collaborate in a multi-disciplinary team, to discover and evolve immunology-related drug discovery pipelines.</p></li><li><p>Individuals with proficiency in computational immunology research are particularly encouraged to apply.</p></li></ul><p>#MDJobs, #MDJobsRGC</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Genetics Medicine, MASH]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49566]]></requisitionid>
    <referencenumber><![CDATA[R49566]]></referencenumber>
    <apijobid><![CDATA[r49566]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49566/medical-director-clinical-development-genetics-medicine-mash/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our MASH/Metabolism team, supporting genetic medicine programs from First in Human through Phase 3. In this role, you will lead cross-functional study teams to shape clinical development strategy and ensure the scientific integrity of trials, while collaborating closely with discovery scientists, translational researchers, and regulatory colleagues.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location: </strong>Tarrytown, NY</li><li><strong>Work model/flexibility: </strong>On-site four days per week</li><li><strong>Travel percentage: </strong>10% to relevant conferences/congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Lead cross-functional teams to craft novel clinical development strategy for genetic medicines</li><li>Partner with discovery and translational scientists to understand emerging genetic targets across MASH, metabolism, rare diseases, and other therapeutic areas</li><li>Author and finalize protocols, amendments, monitoring plans, SAPs, and regulatory submissions</li><li>Evaluate the benefits and risks of assigned therapeutic candidates to inform program decisions</li><li>Oversee trial execution, including adverse event review and ongoing monitoring of patient health and data quality</li><li>Ensure team compliance with FDA, EMA, ICH, and GCP guidelines</li><li>Conduct literature reviews to identify development opportunities from mechanistic, pharmacological, and clinical perspectives</li><li>Represent clinical science in communications and meetings with regulatory agencies</li></ul><br><h3>This role requires:</h3><ul><li>M.D. degree (M.D./Ph.D. or prior research experience preferred)</li><li>Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred)</li><li>2-3+ years of clinical practice or industry experience preferred</li><li>Track record of success in clinical or scientific research settings</li></ul><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Centro (Ematologia)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49792]]></requisitionid>
    <referencenumber><![CDATA[R49792]]></referencenumber>
    <apijobid><![CDATA[r49792]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49792/key-account-manager-centro-ematologia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Costruiamo insieme il nostro futuro:</strong></p><p>In Regeneron utilizziamo la scienza e l’innovazione per sviluppare farmaci che cambiano la vita delle persone con malattie gravi. Cerchiamo un Senior Sales Specialist, Ematologia Commerciale, Italia da inserire nel nostro team vendite di ematologia. La posizione supporterà il business italiano con un modello di lavoro sul territorio. In questo ruolo, promuoverai la crescita del territorio e relazioni di valore con i professionisti sanitari. Collaborerai con i colleghi dell’area medica e con altre funzioni. Questa posizione offre l’opportunità di contribuire a un’organizzazione in rapida crescita, guidata dalla scienza e orientata ai pazienti.</p><p><strong>Quando e dove:</strong></p><p>Italia Centro<br>Posizione sul territorio, con trasferte frequenti.</p><p><strong>Scopri il tuo ruolo:</strong></p><ul><li><p>Costruire relazioni di qualità con i professionisti sanitari utilizzando conoscenze scientifiche aggiornate e messaggi di vendita approvati.</p></li><li><p>Attuare i piani commerciali e di marketing per raggiungere gli obiettivi di vendita e gli indicatori di performance.</p></li><li><p>Gestire gli account strategici attraverso pianificazione, targeting e segmentazione, in linea con le indicazioni regionali.</p></li><li><p>Sviluppare piani locali per gli account utilizzando dati di mercato e aggiornarli in base alle dinamiche del mercato.</p></li><li><p>Collaborare con i colleghi dell’area medica su programmi regionali a supporto delle esigenze dei professionisti sanitari.</p></li><li><p>Rappresentare Regeneron Ematologia in congressi e incontri regionali, nazionali e internazionali.</p></li><li><p>Utilizzerai canali diretti e digitali per ottimizzare il coinvolgimento e contribuire al miglioramento della pratica clinica.</p></li></ul><p><strong>Questo ruolo richiede:</strong></p><ul><li><p>Laurea o qualifica equivalente riconosciuta per i professionisti delle vendite.</p></li><li><p>Almeno cinque anni di esperienza nelle vendite farmaceutiche, inclusa un’esperienza essenziale in ematologia.</p></li><li><p>Conoscenza del Codice della Federazione Europea delle Industrie e Associazioni Farmaceutiche e delle normative locali applicabili.</p></li><li><p>Ottima conoscenza dell’italiano; la conoscenza dell’inglese costituisce un vantaggio.</p></li><li><p>Attitudine tecnica alla vendita basata sulla patologia e sui concetti scientifici.</p></li><li><p>Capacità di utilizzare dati, sistemi multipli e piattaforme di Customer Relationship Management.</p></li><li><p>Eccellenti capacità di coinvolgimento del cliente, presentazione, pianificazione e definizione delle priorità.</p></li><li><p>Capacità di lavorare autonomamente entro scadenze ristrette, dimostrando integrità e una comunicazione etica.</p></li><li><p>esperienza nel lancio di prodotti costituisce un vantaggio.</p></li></ul><p><strong>Salary Range (annually)</strong></p><p> € 59.325 - € 98.875</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Systems Administrator, Infrastructure]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48763]]></requisitionid>
    <referencenumber><![CDATA[R48763]]></referencenumber>
    <apijobid><![CDATA[r48763]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48763/senior-automation-systems-administrator-infrastructure/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Automation System Administrator to join our IOPS team, supporting the administration and compliance of automated and computerized system software and firmware across our biopharmaceutical manufacturing environment. In this role, you will specify and maintain software configurations for process, monitoring, and testing systems — ensuring systems remain in a qualified and compliant state throughout their lifecycle — while collaborating with Manufacturing, Quality Control, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Menands, New York, United States</li><li>Work model/flexibility: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Administer system applications including user access control, user groups, and security settings; monitor data backup and archival to ensure systems meet defined RTO and RPO targets</li><li>Maintain configuration management and recipe and method management; conduct system integration with existing platforms such as LIMS and Historian</li><li>Ensure systems remain in a compliant state by processing change control requests including requirement and design specifications, test plans, technical evaluations, and quality risk assessments</li><li>Author impact statements, Configuration Specifications, risk assessments, SOPs, Work Instructions, policies, and corrective and preventive action plans</li><li>Support and lead system SAT/FAT, validation, and qualification efforts; participate in, lead, or author investigations and root cause analyses for non-compliance issues</li><li>Provide end-user support including system functionality training, application-level troubleshooting, and hardware support in coordination with vendors</li><li>Lead aspects of work for contractors and provide guidance as applicable; drive continuous process improvement across automation systems and procedures</li><li>Evaluate new software for functional equivalence and support validation activities to demonstrate suitability across the system lifecycle</li><li>Experience with process control systems and product release testing systems in a regulated manufacturing or laboratory environment preferred</li><li>Familiarity with Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms a plus</li><li>Solid understanding of System Design Lifecycle and Quality Risk Management</li><li>Familiarity with regulatory and quality policies, procedures, and documentation methods in a cGMP environment</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Science, Engineering, or a related field</li><li>Automation Systems Administrator: 2+ years of relevant experience</li><li>Senior Automation Systems Administrator: 5+ years of relevant experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Corporate Compliance Coordinator – Risk Navigation and Advisory Services]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47747]]></requisitionid>
    <referencenumber><![CDATA[R47747]]></referencenumber>
    <apijobid><![CDATA[r47747]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47747/senior-corporate-compliance-coordinator-risk-navigation-and-advisory-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>Regeneron is looking for an outstanding Senior Corporate Compliance Coordinator to join our Risk Navigation and Advisory Services team within Corporate Compliance, reporting to the Senior Director, Corporate Compliance, in an on-site work model. In this role, you will provide day-to-day operational and administrative support and contribute substantively to project-based compliance initiatives, working closely with colleagues across Corporate Compliance.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Sleepy Hollow, NY</li><li>Work model/flexibility: 4 days Onsite</li></ul><h3>Discover your role:</h3><ul><li>Maintaining and administering compliance documentation, records, and tracking systems.</li><li>Proofreading and quality-reviewing guidance documents, standard operating procedures, communications, and other formal materials.</li><li>Crafting high-quality presentations, communications, and visual materials to support compliance training, leadership updates, and client communications.</li><li>Analyzing data and maintaining compliance metrics to inform communications, training, and monitoring efforts.</li><li>Supporting the planning and execution of compliance-related events, including live training and National Meetings.</li><li>Responding to routine internal inquiries related to compliance policies and escalating issues as appropriate.</li><li>Supporting special projects assigned by management in support of Corporate Compliance objectives.</li><li>Researching and evaluating approved AI and automation tools to improve compliance workflows, documentation, and analytical capabilities.</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree in Business, Law, Life Sciences, Communications, or a related field preferred.</li><li>0–2 years of relevant professional experience; prior internship or coursework in compliance, legal, regulatory, or related fields is a plus.</li><li>Strong proficiency in Microsoft Office Suite, with particular emphasis on Word (templates, formatting), Excel (data analysis, pivot tables, formulas), and PowerPoint (design, presentation development).</li><li>Proven knowledge of and hands-on experience with AI productivity tools (e.g., Microsoft Copilot, ChatGPT, or comparable platforms), and an eagerness to explore new AI applications in a business setting.</li><li>Must have strong organizational skills and attention to detail, with the ability to manage multiple tasks simultaneously.</li><li>Possess excellent written and verbal communication skills and prepare clear, professional materials for diverse audiences.</li><li>Comfortable engaging with colleagues across levels of the organization in an in-person office environment.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Dermatology Medical Specialist I - Dermatology - Phoenix North Territory]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49852]]></requisitionid>
    <referencenumber><![CDATA[R49852]]></referencenumber>
    <apijobid><![CDATA[r49852]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49852/dermatology-medical-specialist-i-dermatology-phoenix-north-territory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Phoenix North Territory</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus</p></li><li><p>We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience</p></li><li><p>Having a minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred.</p></li><li><p>This role requires the ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QC Microbiology Scientist]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49149]]></requisitionid>
    <referencenumber><![CDATA[R49149]]></referencenumber>
    <apijobid><![CDATA[r49149]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49149/qc-microbiology-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> QC Microbiology Associate Scientist / Scientist</strong> to join our <strong>QC Tech Resources </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Validating methods and equipment related to sterility, bioburden, endotoxin testing, and microbial identifications.</p></li><li><p>Writing technical documentation, including position papers, validation reports, and microbiological investigations.</p></li><li><p>Culturing organisms, conducting research, and characterizing them for use in investigations and cleaning development.</p></li><li><p>Reviewing new test procedures and assays for accuracy and compliance.</p></li><li><p>Evaluating and acquiring new methodologies, techniques, and equipment as needed.</p></li><li><p>Overseeing contract laboratory testing to ensure quality and compliance.</p></li><li><p>Setting product specifications and alert/action levels for microbiological standards.</p></li><li><p>Leading technical troubleshooting and problem investigations.</p></li><li><p>Reviewing assay, process, and equipment validation reports, as well as other technical documents for correctness and regulatory compliance.</p></li><li><p>Coaching junior team members on good microbiology lab practices and modern aseptic techniques.</p></li><li><p>Supporting and participating in regulatory inspections to ensure compliance.</p></li><li><p>Demonstrating investigational skills and working knowledge of microbiology assay development and validation.</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have a proven record to work independently or as part of a team.</p></li><li><p>Possessing a strong background in pharmaceutical microbiology, GMP working experience in QC labs, and aseptic techniques.</p></li><li><p>You possess strong trouble-shooting and problem solving skills.</p></li><li><p>You have strong attention to detail & excellent written and oral skills.</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>Assoc QC Microbiology Scientist: Minimum 0-2 years of Experience</p></li><li><p>QC Microbiology Scientist: Minimum 2 years of Experience</p></li><li><p>To be considered for this opportunity you should have a BS/BA or equivalent experience in Microbiology or related field and 2+ years of validated experience, or equivalent combination of education and experience.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQC</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Compliance Specialist External Manufacturing]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49404]]></requisitionid>
    <referencenumber><![CDATA[R49404]]></referencenumber>
    <apijobid><![CDATA[r49404]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49404/compliance-specialist-external-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Compliance Specialist External Manufacturing </strong>to join our <strong>Drug Product Manufacturing </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide</p><p><strong>When & where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Leading and managing CAPAs and change controls</p></li><li><p>Reviewing and maintaining procedures, polices and other instructional documents with a focus on continuous improvement</p></li><li><p>Generating and tracking performance metrics</p></li><li><p>Maintaining knowledge of current good manufacturing practices cGMPs</p></li><li><p>Performing periodic reviews of Drug Product Manufacturing documentation and records to assess for compliance with established quality standards, policies and procedures</p></li><li><p>Travelling to contract manufacturers or business partners, as required (25% or less)</p></li><li><p>Maintaining required training status on Regeneron specific work instructions and SOP’s</p></li><li><p>Assisting in maintenance of product integrity and company reputation by assisting in the monitoring of cGMP compliance at drug product contract manufacturers</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Able to prioritise, re-prioritise as needed and adapt to change</p></li><li><p>Comfortable working in a fast-paced setting</p></li><li><p>Ability to work independently or as part of a team</p></li><li><p>Meets commitments on scope and on time</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Associate Specialist: 0-2 years of related experience in cGMP manufacturing operations (clinical and/or commercial drug products)</p></li><li><p>Specialist: 2+ years of related experience in cGMP manufacturing operations (clinical and/or commercial drug products)</p></li><li><p>May consider equivalent combination of education and experience. Level will be determined based on qualification and experience relevant to the role</p></li></ul><p>Thrive today. Grow tomorrow.</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager - Hematology (f/m/d) - Germany North-East]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49847]]></requisitionid>
    <referencenumber><![CDATA[R49847]]></referencenumber>
    <apijobid><![CDATA[r49847]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49847/key-account-manager-hematology-fmd-germany-north-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hematology to join our International Hematology team, supporting Germany in a field-based work mode. In this role, you will drive account performance and regional contracting activities for our hematology portfolio while collaborating with Medical colleagues, pharmacists, hospital stakeholders, and commercial teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Field-based in Germany North-East</p><p><strong>Discover your role:</strong></p><ul><li><p>Establish high-quality healthcare professional relationships across the territory</p></li><li><p>Develop referral networks spanning hospital, outpatient, and office-based settings</p></li><li><p>Deliver portfolio value messages through face-to-face, remote, and digital engagement</p></li><li><p>Partner with Medical on regional programs and healthcare professional activities</p></li><li><p>Manage account planning, segmentation, targeting, and local account plans</p></li><li><p>Support regional contracting activities and adapt contract models to local needs</p></li><li><p>Analyze market trends and competitor activity to inform negotiations</p></li><li><p>Thrive in an agile environment and adjust priorities to account needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or recognized equivalent for sales professionals</p></li><li><p>5-7 years of progressive pharmaceutical or biotechnology sales experience</p></li><li><p>Knowledge of the German healthcare system and regional market structures</p></li><li><p>Experience using data, customer relationship management systems, and multiple business systems</p></li><li><p>Qualification in applicable pharmaceutical industry codes, including EFPIA Code or VFA Pharmakodex</p></li><li><p>Fluency in German and good working knowledge of English</p></li><li><p>Ability to manage a large territory independently with frequent travel</p></li><li><p>Strong customer engagement, negotiation, and communication skills</p></li><li><p>High integrity and ethical standards in all interactions</p></li><li><p>Hematology sales experience and an established network strongly preferred</p></li><li><p>Experience supporting hospital, purchasing group, or payer contract negotiations preferred</p></li><li><p>Product launch experience preferred</p></li></ul><p>Salary range (annually)</p><p>73,125 -121,875 €</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Biostatistics - Immunology & Inflammation]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46192]]></requisitionid>
    <referencenumber><![CDATA[R46192]]></referencenumber>
    <apijobid><![CDATA[r46192]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46192/senior-director-biostatistics-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Director </strong>to lead our <strong>Biostatistics </strong><strong>Immunology & Inflammation</strong> therapeutic area.</p></div><div><p>The incumbent will have responsibility for strategic and operational activities and for assisting the Head, Biostatistics in the development and implementation of departmental scientific policies, operational guidelines, and administrative structure. The incumbent could also serve as senior research expert, with demonstrated ability to be a leader within Global Development and within the field for specific statistical methodology or application. The successful candidate should have a track record in leading teams and the ability to effectively structure a function to manage the anticipated growth in the product pipeline. They must also possess excellent communication skills to interface with senior leadership on behalf of the department and work closely with medical study directors to provide and receive direction on clinical programs and have the ability to influence the medical and clinical teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Cambridge, MA or Warren, NJ</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Determining Department goals and resource allocation in conjunction with the Department Executive Director.</p></li><li><p>Ensure project teams have high quality statistical support for creation of clinical development plans, study design, and operational aspects.</p></li><li><p>Work with senior management to ensure statistical representation in key project decisions and regulatory meetings. Serve as departmental representative on corporate‐wise teams.</p></li><li><p>Oversee process for statistical reporting. Review critical documents, such as SAP, analysis results presentations, CSR, and integrated summaries. Ensure compliance with data submission guidelines.</p></li><li><p>Plan and track project activities, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization across projects or areas. Effect long‐range planning.</p></li><li><p>Ensure technical direction and mentoring for staff. Encourage personal development in the context of project work. Learn and apply techniques to promote teamwork, quality, and motivation. Recruit, develop, and retain high quality staff.</p></li><li><p>Maintain awareness of industry standards and regulatory requirements. Alert staff to new or changing standards. Within area of control, harmonize policies with departmental guidelines SOPs and with industry standards. Develop polices promoting application of corporate values in work practices.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D. in statistics or related discipline with 10+ years of experience (or MS in statistics or related discipline with 15+ years) in the biotechnology, pharmaceutical or health related industry, including significant interaction with both FDA and EMEA, history of successful project and people management (6+ years), and expertise in multiple therapeutic areas.</p></li><li><p>Active research interests in area related to clinical trial.</p></li><li><p>Demonstrated ability to work in a changing and busy environment and to exercise judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks.</p></li><li><p>Ability to work independently – self‐directed, high energy and strong work ethic. High degree of creativity, latitude and attention to detail required.</p></li><li><p>Demonstrated strong leadership, project management, teamwork and interpersonal skills.</p></li><li><p>Excellent presentation skills.</p></li><li><p>Experience and proven ability leading and managing major process and technology initiatives with utilization and impact across multiple functional groups.</p></li><li><p>Broad knowledge and superior understanding of advanced statistical concepts and techniques.</p></li><li><p>Outstanding ability and skills to effectively represent Biostatistics and Data Management in interactions with senior management or cross‐functional committees.</p></li><li><p>Thorough knowledge of pharmaceutical clinical development and life cycle management; ability to innovatively apply technical principles, theories and concepts to clinical drug development leading to regulatory approvals.</p></li><li><p>Thorough working knowledge of regulatory guidelines on drug development, regulatory submissions, and statistical practice.</p></li><li><p>Understanding of the drug discovery and development process, regionally and globally.</p></li><li><p>Strong administrative skills.</p></li><li><p>Ability to influence others to achieve results.</p></li></ul><p>#GDBDMJobs</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist, Talent Operations and Solutions]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49850]]></requisitionid>
    <referencenumber><![CDATA[R49850]]></referencenumber>
    <apijobid><![CDATA[r49850]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49850/senior-specialist-talent-operations-and-solutions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>We are looking for a Senior Specialist, Talent Operations to serve as a senior operational authority for Regeneron’s expanded Talent organization, reporting to the Manager, Talent Operations and Solutions. This role owns the data accuracy, vendor relationships, and process quality behind the events, procurement, and programs that enable our Talent Acquisition, Talent Management, Culture & Inclusion, and Learning & Development teams to deliver on their strategic priorities. You’ll evaluate how things run today, spot where processes break down across teams or geographies, and recommend fixes that hold up broadly — managing enterprise-facing events, owning the purchase order process end to end, building playbooks, and mentoring newer team members along the way.</p><br><h3>When & where:</h3><ul><li>Location: Sleepy Hollow, NY</li><li>Work model: Onsite 4 days per week</li></ul><br><h3>Discover your role:</h3><h3>Event Planning & Execution</h3><ul><li>Lead end-to-end logistics for enterprise-facing Talent events — leadership convenings, offsites, learning forums, recruiting/campus events, and signature internal conferences — and continuously improve event playbooks for consistency across teams.</li><li>Serve as the escalation point for complex logistical, vendor, or stakeholder issues, partnering with external vendors and cross-functional teams (AV, Security, Facilities, Creative Services, Procurement) to keep deliverables on track.</li><li>Oversee post-event logistics, asset management, and reporting to keep attendance, spend, and outcome data accurate for future planning.</li></ul><h3>Procurement & Purchase Order Administration</h3><ul><li><h3>Own and administer the purchase order process for the Talent organization, ensuring data accuracy and integrity of PO and spend records across all four functions.</h3></li><li>Advise stakeholders on procurement policy and vendor contract considerations, and continuously improve PO workflows and vendor management practices across the function.</li><li>Prepare metrics, analytics, and dashboards on committed and actual spend to support budget decisions and flag risk early.</li></ul><h3>Operations & Program Infrastructure</h3><ul><li>Own data accuracy and integrity across the Talent portfolio’s operational infrastructure — workplans, trackers, calendars, status updates, and decision records.</li><li>Resolve escalated inquiries from Talent Acquisition, Talent Management, Culture & Inclusion, and Learning & Development that require deeper program or policy knowledge.</li><li>Mentor less experienced coordinators and associates, serving as a subject matter resource on tools, systems, and processes.</li></ul><h3>TA Systems, Vendor & Candidate Support</h3><ul><li>Support enhancements to TA’s core systems (ATS, CRM, CMS), including issue resolution, reporting, and administration.</li><li>Own vendor relationships for the recruiting technology stack — product updates, contract renewals, and business reviews.</li><li>Serve as point of contact for external candidate inquiries, partnering with the careers website team to resolve issues.</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA in a related field plus 5+ years of experience in program operations, event management, HR/People operations, procurement administration, or a similar role.</li><li>Demonstrated proficiency in procedure writing, auditing, HRIS/TA systems, or vendor management.</li><li>Experience owning or administering a purchase order, procurement, or budget-tracking process.</li><li>Strong written and verbal communication skills, with the ability to advise stakeholders confidently.</li><li>Proficiency in Microsoft Office (PowerPoint and Excel in particular) and comfort working in Teams/SharePoint and managing trackers.</li><li>Familiarity with Workday, Beamery, or similar HR/talent platforms, and enterprise procurement/invoicing systems.</li><li>Experience in pharmaceutical, biotech, or large matrixed organizations.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Baltimore, MD]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48096]]></requisitionid>
    <referencenumber><![CDATA[R48096]]></referencenumber>
    <apijobid><![CDATA[r48096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48096/medical-specialist-i-pulmonology-baltimore-md/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Baltimore]]></city>
    <state><![CDATA[Maryland]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Baltimore, MD - representative must reside within the territory (e.g. Baltimore, Dover, Bel Air).</strong></p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups.</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p>​<strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Scientific Marketing Lead (NSCLC)]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49930]]></requisitionid>
    <referencenumber><![CDATA[R49930]]></referencenumber>
    <apijobid><![CDATA[r49930]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49930/director-scientific-marketing-lead-nsclc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, NSCLC Scientific Marketing Lead is a strategic leadership role within Regeneron's US Oncology Commercial organization. This position is responsible for leading the overall NSCLC Scientific Marketing strategy and organization, serving as the critical link between the commercial organization and the scientific community to drive awareness, education, and engagement for the product.</p><p>Reporting to the US NSCLC Brand Lead, the Director provides strategic leadership for scientific marketing initiatives, thought leader engagement, and field-based scientific marketing activities, ensuring alignment with the overall US brand strategy. The role is a 2nd line leader role with Scientific Marketers and field based marketers reporting up through to them.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY office for 4 days a week with travel approximately for Congresses, Ad Boards, POA including occasional weekend travel/meetings as business needs require (~25% of the time)</li></ul><h3>Discover your role:</h3><ul><li>Lead the development and execution of the US NSCLC Scientific Marketing strategy and annual business plan aligned with overall brand objectives</li><li>Own the scientific marketing budget, including resource allocation, investment decisions, forecasting, and delivery of key strategic initiatives</li><li>Establish and oversee NSCLC KOL engagement strategy, advocacy plan, and insight generation priorities</li><li>Build and maintain strategic relationships with leading academic and community oncology experts across NSCLC</li><li>Oversee advisory boards, steering committee engagements, speaker programs, congress activities, and other scientific engagement initiatives to generate actionable insights</li><li>Drive KOL mapping and engagement strategies across national, regional, and local levels to ensure comprehensive customer coverage and insight generation</li><li>Lead and evolve the US TLL strategy and scientific engagement model, ensuring alignment with brand priorities and customer needs</li><li>Serve as a key member of the US NSCLC Brand Team, providing ongoing tumor area expertise and delivering strategic recommendations based on market dynamics and customer insights</li><li>Partner closely with NSCLC Marketing leadership to ensure seamless integration and execution of brand strategy, customer engagement plans, and educational initiatives</li><li>Collaborate with Medical Affairs, Key Account Marketing, and other cross-functional partners to support aligned customer engagement strategies</li><li>Lead congress strategy and scientific presence planning, including sponsorship opportunities, scientific engagement activities, and collaborator interactions</li><li>Monitor and evaluate tactical plan effectiveness through key performance indicators, insight reporting, and business impact assessments</li><li>Ensure all programs, engagements, and materials follow legal, regulatory, corporate, and ethical requirements</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree required; advanced degree (MBA, PhD, PharmD, MD, MS, or equivalent) preferred</li><li>12+ years of pharmaceutical, biotechnology, healthcare, or related industry experience</li><li>8-10 years of experience in oncology marketing, scientific marketing, medical affairs, or commercial leadership roles</li><li>Demonstrated success developing and driving KOL engagement, thought leader advocacy, and scientific exchange strategies</li><li>Proven leadership experience managing and developing high-performing teams</li><li>Strong understanding of oncology clinical practice, scientific data, and treatment landscapes</li><li>Experience leading advisory boards, congress strategy, speaker bureau programs, and scientific engagement initiatives</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Imaging Scientific Director (Oncology)]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48148]]></requisitionid>
    <referencenumber><![CDATA[R48148]]></referencenumber>
    <apijobid><![CDATA[r48148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48148/clinical-imaging-scientific-director-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Clinical Imaging Scientific Director for Oncology</strong> will own the strategy and execution of sophisticated early and late phase oncology imaging in clinical trials where imaging plays a key role. Imaging includes all modalities with a special focus on PET and CT. In this role, you will champion the development of imaging endpoints and biomarkers and drive the scientific imaging aspects as well as tumor response assessment of oncology clinical studies.<br><br>The successful candidate will be an independent imaging scientific leader and a member of cross-functional program teams including Regeneron clinical and preclinical colleagues as well as external academic and industry partners. This position provides excellent opportunities to develop innovative imaging endpoints and biomarkers in support of clinical development and contribute to bringing new treatment options to patients.</p><p><strong>When & Where: </strong>Tarrytown, NY </p><p><strong>Discover your role:</strong></p><ul><li><p>Create fit-for-purpose imaging biomarker strategies and work closely with research, clinical imaging and the oncology therapeutic area for the development of imaging endpoints to inform and advance the Regeneron clinical pipeline.</p></li><li><p>Prepare and present clinical imaging strategies to senior management.</p></li><li><p>Manage a complex network of stakeholders across Regeneron.</p></li><li><p>Lead, design and implement multi-modality imaging measures as endpoints for oncology therapeutic clinical studies.</p></li><li><p>Collaborate closely with Regeneron clinical teams as imaging subject matter expert to ensure optimal design and execution of imaging strategy including development of protocols, imaging endpoints, imaging manuals, imaging charters, statistical analysis plans and clinical study reports.</p></li><li><p>Work closely with Clinical Imaging Operations and imaging contract research organizations to ensure the flawless conduct and data integrity of studies’ imaging components and endpoints.</p></li><li><p>Serve as Study Scientific Director for clinical trials focused on qualification and utilization of novel imaging biomarkers.</p></li><li><p>Lead the interaction with regulatory agencies for communications regarding imaging endpoints and procedures.</p></li><li><p>Lead the interaction with regulatory agencies and site ethics committees for approval of clinical imaging biomarker development studies</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD program with a minimum of 10+ years of clinical imaging experience (minimum of 7 years within oncology drug development).</p></li><li><p>Superior written/verbal communication and organization skills.</p></li><li><p>Experience implementing central efficacy assessments using tumor response criteria such as RECIST 1.1, iRECIST, PCWG3, Lugano and IMWG in oncology clinical trials is needed. </p></li><li><p>We also are looking for you to have had successful engagement experience with regulatory agencies and the ability to champion imaging innovations and lead projects effectively.</p></li><li><p>Experience as study scientific director of PET imaging biomarker clinical trials in Oncology.</p></li><li><p>Experience applying PET imaging as a quantitative endpoint in clinical and preclinical studies in Oncology.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Facilities Engineer]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47148]]></requisitionid>
    <referencenumber><![CDATA[R47148]]></referencenumber>
    <apijobid><![CDATA[r47148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47148/senior-facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><div><div><ul><li><p>Building and specifies cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</p></li></ul></div><ul><li><p>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</p></li></ul><div><ul><li><p>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</p></li></ul></div><div><ul><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li></ul></div><div><ul><li><p>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</p></li></ul></div><div><ul><li><p>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</p></li></ul></div><div><ul><li><p>Implementing corrective/preventative actions for existing equipment and maintenance processes</p></li></ul></div><div><ul><li><p>Preparing engineering evaluations and test plans for and executes modification change control documentation</p></li></ul></div><div><ul><li><p>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs </p></li></ul></div></div><div><div><ul><li><p>Maintains a clean and safe working environment by enforcing procedures, policies, and regulations</p></li></ul></div></div><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have strong analytical and interpersonal skills</p></li><li><p>You are able to prioritise and re-prioritise as needed and adapt to change</p></li><li><p>You are comfortable working in a fast-paced setting</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Sr Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 5 years’ experience </p></li></ul><div><ul><li><p>Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 2 years’ experience </p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director of Operations, CMC Regulatory Sciences]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49384]]></requisitionid>
    <referencenumber><![CDATA[R49384]]></referencenumber>
    <apijobid><![CDATA[r49384]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49384/director-of-operations-cmc-regulatory-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director to join our Regulatory Sciences team, to turn strategy into execution. Someone who is operationally minded, enjoys building and improving processes, develops high-performing teams, and isn't afraid to roll up their sleeves to remove roadblocks and drive results.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead and manage a team responsible for authoring and coordinating CMC regulatory submissions across all modalities — biologics, small molecule, cell and gene therapy, and combination products — from IND/CTA through NDA/BLA and post-approval lifecycle</li><li>Develop and implement global CMC regulatory strategies for product development and lifecycle management, aligning with business objectives and accelerating time to approval</li><li>Build and continuously improve team processes, templates, workflows, and submission tracking systems to increase throughput and consistency, enabling the team to reliably meet aggressive and shifting timelines</li><li>Establish and track operational metrics such as cycle time, submission quality, and on-time delivery to identify bottlenecks and drive measurable improvements in team efficiency</li><li>Manage team capacity and workload distribution across concurrent submissions, proactively identifying resourcing gaps and reallocating support during peak submission periods</li><li>Mentor, coach, and develop staff to build bench strength and technical capability; represent the company in industry professional associations to help shape the external regulatory environment</li><li>Demonstrated experience managing or leading a team with a track record of developing talent and scaling team output</li><li>Strong working knowledge of FDA, EMA, and international CMC regulations and guidance across multiple modalities</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>BS/BA in a life sciences discipline required</li><li>Associate Director: 10+ years of experience in the healthcare or biotech industry</li><li>Director: 12+ years of experience in the healthcare or biotech industry</li><li>Senior Director: 15+ years of experience in the healthcare or biotech industry</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$147,800.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Administrative Coordinator, Internal Medicine Clinical Development Unit]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49856]]></requisitionid>
    <referencenumber><![CDATA[R49856]]></referencenumber>
    <apijobid><![CDATA[r49856]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49856/senior-administrative-coordinator-internal-medicine-clinical-development-unit/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Administrative Coordinator</strong> to join our team, supporting the VP Therapeutic Area Lead and Cardiovascular Renal Metabolic (CVRM) Clinical Development team based on-site in Tarrytown, NY. In this role, you will proactively manage calendars, coordinate travel and meeting logistics, and help teams execute day-to-day objectives, while collaborating with leaders, administrative peers, and cross-functional partners like IT, Facilities, and Procurement.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY</p></li><li><p><strong>Work model/flexibility:</strong> 4 days a week on-site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Anticipate the needs of leaders and teams, solving logistics before they become problems</p></li><li><p>Own coordination of internal and external meetings, seminars, and events from start to finish</p></li><li><p>Bring organization to team town halls, offsites, and agendas that keep people aligned</p></li><li><p>Navigate ambiguity and shifting priorities with composure and good judgment</p></li><li><p>Build trusted relationships across all levels, while keeping sensitive information confidential</p></li><li><p>Step in as backup support for fellow coordinators when the team needs it</p></li><li><p>Stay curious and pick up new tools and systems quickly, for yourself and those you support</p></li><li><p>Bring a collaborative, solutions-first mindset to daily administrative workflows</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Associate's or Bachelor's degree preferred; 5+ years of administrative experience (years of relevant experience may be considered in lieu of degree)</p></li><li><p>2+ years of industry experience in a relevant business function, desirable</p></li><li><p>Strong written and verbal communication skills, with the ability to interact confidently across all levels of the organization</p></li><li><p>Demonstrated independence, sound judgment, and problem-solving ability</p></li><li><p>A track record of building effective relationships up, down, and across teams</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$33.80 - $52.93]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47968]]></requisitionid>
    <referencenumber><![CDATA[R47968]]></referencenumber>
    <apijobid><![CDATA[r47968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47968/senior-manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Regulatory Affairs Advertising and Promotion team. This position requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidance to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). They will provide regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with minimal guidance from the Regulatory Affairs, Advertising and Promotion Director. The Senior Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US and Global (if applicable) regulatory activities associated with advertising and promotion of the company’s marketed products, as well as commercial development of pipeline products. Manages commercial activities from a regulatory advertising and promotion perspective with minimal guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with minimal guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with minimal guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Provide input to direct management with respect to process improvement for promotional review activities and establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With minimal guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 3 to 4 years within regulatory affairs, preferably within advertising and promotion</p></li><li><p>At minimum, a Bachelor’s degree (BS) from an accredited College or University in Life Sciences. Advanced degree (Masters, Pharm D, Ph.D., MD or DO) preferred in the field of medicine or science. Regulatory experience can offset education requirements.</p></li><li><p>Advance knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and managing launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Ability to influence cross-functional teams and interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47967]]></requisitionid>
    <referencenumber><![CDATA[R47967]]></referencenumber>
    <apijobid><![CDATA[r47967]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47967/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager </strong>to join our<strong> Regulatory Affairs Advertising and Promotion</strong> team. In this role, you will apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY- SEATTLE, WA / PORTLAND, OR]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48074]]></requisitionid>
    <referencenumber><![CDATA[R48074]]></referencenumber>
    <apijobid><![CDATA[r48074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48074/medical-account-specialist-ii-neurology-seattle-wa-portland-or/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Seattle]]></city>
    <state><![CDATA[Washington]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Seattle (Metro), WA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 15:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology (CO, MO, KS, OK and NM)]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50063]]></requisitionid>
    <referencenumber><![CDATA[R50063]]></referencenumber>
    <apijobid><![CDATA[r50063]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50063/associate-director-field-medical-affairs-hematology-co-mo-ks-ok-and-nm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Territory: CO, MO, KS, OK and NM (ideally to reside in CO or St. Louis) <br><strong>Travel:</strong> Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. <br> </p><p>#medicalscienceliaison #msl #HFM #AD<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Facilities Maintenance]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49114]]></requisitionid>
    <referencenumber><![CDATA[R49114]]></referencenumber>
    <apijobid><![CDATA[r49114]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49114/senior-director-facilities-maintenance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Facilities Maintenance to lead equipment maintenance and calibration for our manufacturing, laboratory, and warehouse operations, ensuring systems supporting drug product filling, visual inspection, device assembly, and packaging remain validated, compliant, and operational. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Onsite, Monday-Friday 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Own the site's preventive and corrective maintenance programs and calibration program for equipment supporting drug product filling, visual inspection, device assembly, packaging, and other manufacturing, laboratory, and warehouse systems.</li><li>Partner with Manufacturing, Quality Assurance, Engineering, EHS, and Supply Chain leadership to align maintenance and calibration strategies with production schedules and business objectives.</li><li>Drive reliability-centered maintenance and continuous improvement initiatives to minimize downtime and maximize equipment availability; own maintenance planning, scheduling, and contractor/vendor oversight.</li><li>Establish and monitor KPIs (equipment uptime, mean time between failures, mean time to repair, maintenance backlog), leveraging OEE and CMMS data to drive condition-based and predictive maintenance.</li><li>Maintain calibration schedules and traceability to national/international standards, ensuring records and systems are always audit-ready; own or support equipment-related deviation investigations, CAPAs, and change controls.</li><li>Ensure all maintenance and calibration activities comply with cGMP, FDA, ISO 13485, and EU GMP Annex 1, and serve as a key stakeholder during regulatory inspections and audits.</li><li>Build, mentor, and develop a high-performing team, establishing clear accountability, succession planning, and career development pathways; champion a culture of safety, quality, and compliance.</li><li>Identify and lead initiatives to improve operational efficiency, reduce costs, and enhance equipment reliability, including support for facility expansion, equipment tech transfer, and new product introductions.</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA and 15+ years of progressive relevant experience in the pharmaceutical industry, or a MS degree and minimum 13 years of relevant experience.</li><li>Experience managing maintenance/calibration programs and CMMS systems (e.g., Blue Mountain, SAP PM, Maximo) required; experience supporting drug filling, visual inspection, device assembly, and/or packaging strongly preferred.</li><li>Strong working knowledge of cGMP, FDA, ISO 13485, and EU GMP Annex 1, with deep understanding of cleanroom systems and equipment supporting sterile/aseptic manufacturing.</li><li>Proven ability to lead cross-functional teams and influence at all levels, with strong financial acumen managing multi-million dollar operating and capital budgets.</li><li>Ability to work in a manufacturing environment, including cleanroom gowning and availability for after-hours facility emergencies, with excellent problem-solving, project management, and organizational skills, including communication during regulatory inspections.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 07:26:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Critical Utilities]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47222]]></requisitionid>
    <referencenumber><![CDATA[R47222]]></referencenumber>
    <apijobid><![CDATA[r47222]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47222/director-critical-utilities/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of Critical Utilities and Facility Management to join our Facilities and Engineering team, supporting our campus Central Utility Plant and MEP operations in an on-site work model. In this role, you will safeguard the reliability, safety, and compliance of our electricity, chilled water, steam, and emergency power systems, ensuring uninterrupted service for 24/7 research and operational needs while collaborating with Engineering, EH&S, and Business Resilience teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><h3>Discover your role:</h3><ul><li>Develop and implement long-term operational strategies for Critical Utilities and Facilities Maintenance programs across a complex pharmaceutical/biotech campus.</li><li>Lead organizational development efforts, including team structure design, workforce planning, and operational model optimization across internal staff and outsourced providers.</li><li>Establish and continuously improve maintenance, reliability, and capital planning programs to strengthen system performance, resiliency, and compliance.</li><li>Provide executive oversight of Central Utility Plant and Powerhouse operations, partnering with operational leadership to ensure safe, uninterrupted utility delivery.</li><li>Collaborate cross-functionally with Engineering, R&D Operations, EH&S, Quality, Procurement, and Capital Projects teams to support infrastructure initiatives and campus growth.</li><li>Drive governance, performance management, and strategic vendor oversight, including metrics development, operational reviews, budget planning, and risk mitigation.</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree in Mechanical, Electrical, Power, Marine, or Energy Engineering, or 15 years of equivalent experience (Navy Nuclear Power School plus 10 years accepted).</li><li>10+ years leading central utility or power-plant operations (chilled water, steam, emergency power) within a hybrid facility management model, plus strong contract-management and vendor-governance skills.</li><li>Proficiency with building automation system (BAS) platforms, such as Metasys, EcoStruxure, or Desigo.</li><li>Proven team-leadership abilities across internal staff and outsourced providers.</li><li>A valid NYS driver's license to support up to 25% travel.</li><li>Turning maintenance data into actionable reliability improvements.</li><li>Holding rigorous safety and regulatory standards in high-risk environments.</li><li>Communicating clearly with researchers, engineers, and executives, and being flexible with travel</li><li>Motivating and coordinating a mixed team of internal technicians, union trades, and third-party providers.</li><li>Balancing hands-on problem solving with strategic planning, budgeting, and long-range asset management.</li><li>Keeping utility plants, chillers, boilers, and generators running with zero unplanned downtime.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr AP Service Delivery Coordinator]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48258]]></requisitionid>
    <referencenumber><![CDATA[R48258]]></referencenumber>
    <apijobid><![CDATA[r48258]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48258/sr-ap-service-delivery-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are seeking a Senior AP Service Delivery Coordinator to join our Finance team. In this role, you will collaborate with Procurement, vendors, and business stakeholders to identify and resolve invoice holds across all sites. You will manage invoice workflows, investigate payment issues, support accounts payable operations, and contribute to process improvements that enhance efficiency and accuracy. This position offers the opportunity to work in a fast-paced global environment while supporting critical financial operations.</p><p><strong>When & Where:</strong></p><p><strong>Hyderabad (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Collaborate with Procurement, vendors, and business stakeholders to identify and clear invoice holds across all locations.</p></li><li><p>Serve as the primary point of contact for resolving invoice hold issues and payment-related inquiries.</p></li><li><p>Review, investigate, and resolve Quick Invoice and Duplicate Invoice queues.</p></li><li><p>Process invoices using 2-way and 3-way purchase order matching within AP workflow and ERP systems.</p></li><li><p>Review and reconcile vendor statements, identify discrepancies, and coordinate resolution with internal teams.</p></li><li><p>Request missing invoices, credit notes, and supporting documentation from vendors when necessary.</p></li><li><p>Manage accounts payable inquiries and ensure prompt resolution of vendor and end-user concerns.</p></li><li><p>Compile, analyze, and report on routine accounts payable transactions to support business requirements.</p></li><li><p>Support departmental objectives through assigned tasks, projects, and continuous process improvements.</p></li><li><p>Leverage AP automation tools, best practices, and accounting principles to improve operational efficiency and accuracy.</p></li><li><p>Build strong relationships with internal stakeholders and external vendors to ensure effective collaboration and issue resolution.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Accounting, Finance, Commerce, Business, or a related field.</p></li><li><p>Minimum 2+ years of Accounts Payable experience.</p></li><li><p>Strong understanding of accounting fundamentals and accounts payable processes.</p></li><li><p>Experience working in a high-volume, fast-paced environment.</p></li><li><p>Strong analytical and problem-solving skills.</p></li><li><p>Excellent organizational skills and attention to detail.</p></li><li><p>Effective verbal and written communication skills in English.</p></li><li><p>Proficiency in Microsoft Office applications, particularly Excel and Outlook.</p></li><li><p>Experience with document scanning, imaging systems, and invoice workflow tools.</p></li><li><p>Knowledge of Oracle ERP systems is preferred.</p></li><li><p>Ability to adapt quickly to changing priorities and business needs.</p></li><li><p>Strong interpersonal skills and commitment to delivering excellent customer service.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 05:26:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Combination Products (Sustaining)]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44518]]></requisitionid>
    <referencenumber><![CDATA[R44518]]></referencenumber>
    <apijobid><![CDATA[r44518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44518/associate-manager-combination-products-sustaining/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Join Regeneron’s Combination Products team and lead the engineering charge that keeps our commercial products safe, reliable, and continuously improving in the hands of patients and providers. As an Associate Manager, Sustaining Engineering, you’ll steer a high-performing team, own design changes from concept to launch, drive risk management with rigor, and orchestrate cross-functional problem solving that elevates patient experience and product quality. You’ll also expand our global reach by filing commercial products in new regions and supporting contract manufacturing operation changes and additions. </p><p><strong>When & where:</strong></p><ul><li><p>East Greenbush, New York, United States</p></li><li><p>Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Turn complaints into insight—feed real‑world experience directly into risk management</p></li><li><p>Partner with development team to share post market feedback for new product development </p></li><li><p>Lead and mentor sustaining engineers across multiple commercial combination products throughout the lifecycle</p></li><li><p>Implement targeted design changes to elevate quality and customer experience</p></li><li><p>Drive and document customer complaint investigations—identify root causes and implement corrective and preventive actions</p></li><li><p>Facilitate design transfer of existing products to new manufacturing sites with rigor and speed</p></li><li><p>Participate in cross‑functional design teams to resolve issues quickly and prevent recurrence</p></li><li><p>Build and grow strong relationships with internal stakeholders and key external partners</p></li><li><p>Demonstrate deep understanding of FDA regulations for combination products, including 21 CFR Part 3 and design controls per 21 CFR 820.30</p></li><li><p>Apply hands‑on expertise in Design History File management and sustaining engineering for medical devices and/or combination products</p></li><li><p>Apply strong analytical problem‑solving skills and deliver clear technical writing and crisp oral communication</p></li><li><p>Lead projects that balance business objectives with technical constraints and keep cross‑functional teams moving</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>B.S in Engineering; Biomedical Engineering, Mechanical Engineering, Industrial Engineering is preferred</p><ul><li><p>Associate Manager sustaining Engineering: 6+ years of experience</p></li><li><p>Manager sustaining Engineering: 7+ years of experience</p></li><li><p>Level will be determined based on experience</p></li></ul></li><li><p>Previous supervisory/ people leadership experience</p></li><li><p>Previous experience in manufacturing of medical devices and/or combination products</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 09:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Triage]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47759]]></requisitionid>
    <referencenumber><![CDATA[R47759]]></referencenumber>
    <apijobid><![CDATA[r47759]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47759/senior-manager-triage/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our safety team, supporting our operations in a hybrid role. In this role, you will lead Individual Case Safety Report triage while collaborating with healthcare professionals and medical reviewers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid - three days a week on site)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead healthcare professionals performing upfront medical triage in Argus Safety.</p></li><li><p>Assess seriousness, expectedness, causality, and reporting timelines for incoming cases.</p></li><li><p>Apply expedited reporting logic, including seven-day and 15-day requirements.</p></li><li><p>Verify source completeness, identify follow-up needs, and assign Argus workflows.</p></li><li><p>Escalate complex cases to the Lead Medical Reviewer.</p></li><li><p>Author structured summaries covering clinical course, causality, and review considerations.</p></li><li><p>Maintain SOP, data privacy, documentation, and inspection readiness standards.</p></li><li><p>You explore artificial intelligence technologies to improve operational efficiency.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>MD, MBBS, PharmD, BDS, MDS, or Nurse Practitioner qualification.</p></li><li><p>8+ years’ industry experience, including 5+ years in pharmacovigilance case processing.</p></li><li><p>Hands-on ICSR intake, Argus Safety, and expedited reporting experience.</p></li><li><p>Knowledge of ICH E2A, E2B, E2D, FDA, EMA, and Health Canada requirements.</p></li><li><p>Ability to interpret Investigator’s Brochures, US Prescribing Information, and Summaries of Product Characteristics.</p></li><li><p>MedDRA coding familiarity and high-volume case processing experience.</p></li><li><p>Strong clinical judgement and concise written communication under pressure.</p></li><li><p>Triage or first-line safety review experience preferred.</p></li><li><p>AI or generative AI experience or interest.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Hematology (f/m/d) - Austria & Switzerland]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50157]]></requisitionid>
    <referencenumber><![CDATA[R50157]]></referencenumber>
    <apijobid><![CDATA[r50157]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50157/key-account-manager-hematology-fmd-austria-switzerland/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hemato-Oncology to join our Commercial Oncology team, supporting Austria and Switzerland. In this role, you will drive sales performance and customer engagement while collaborating with cross-functional stakeholders and healthcare professionals. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Austria, field-based</p><p>Frequent travel across Austria and Switzerland. Occasional evening and weekend work.</p><br><p><strong>Discover your role:</strong></p><br><ul><li>Build scientific relationships with healthcare professionals across hematology-oncology.</li><li>Develop and update account plans using market insights and key data.</li><li>Execute marketing strategies aligned with territory and account priorities.</li><li>Deliver sales objectives through effective territory budget management.</li><li>Collaborate with stakeholders to achieve shared business objectives.</li><li>Peer-coach sales colleagues and share best practices across the team.</li><li>Contribute to special projects, events, and strategic business initiatives.</li><li>You bring a patient-focused mindset and create value in every interaction.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>Bachelor's degree or similar educational background as well as a successfully completed "Pharmareferentenprüfung" or equivalent academic qualification.</li><li>8-10+ years of biotech or pharmaceutical sales experience.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Previous experience in biologics and oncology disease areas.</li><li>Significant oncology and/or hematology experience across multiple disease areas.</li><li>Strong knowledge of Austrian and Swiss healthcare systems and market structures.</li><li>Established network of relevant healthcare professionals.</li><li>Knowledge of healthcare compliance codes and promotional regulations.</li><li>Fluency in written and spoken German and English.</li><li>Strong customer engagement, presentation, planning, and organizational skills.</li><li>Ability to work independently and execute strategic and tactical plans under tight timelines.</li><li>High integrity, ethical conduct, and effective communication skills.</li><li>Willingness to travel frequently across Austria and Switzerland.</li><li>Experience in Multiple Myeloma, Follicular Lymphoma, and/or DLBCL preferred.</li><li>Experience working across Austria and Switzerland preferred.</li></ul><br><br><p>For this position, the Collective Bargaining Agreement for Trade (Kollektivvertrag Handel) applies; depending on qualifications and professional experience, we offer a salary above the collectively agreed minimum.</p><br><p><strong>Salary Range (annually)</strong></p><p>72.075,00 € - 120.125,00 €</p><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Administrative Coordinator, Regulatory Affairs]]></title>
    <date><![CDATA[Fri, 21 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50068]]></requisitionid>
    <referencenumber><![CDATA[R50068]]></referencenumber>
    <apijobid><![CDATA[r50068]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50068/administrative-coordinator-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Administrative Coordinator to join our Regulatory Affairs team, supporting our Japan Regulatory Affairs organization in a hybrid work model. In this role, you will provide administrative and operational support to local and global Regulatory Affairs activities while collaborating with Regulatory Affairs, safety, Human Resources, Talent Acquisition, and global colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Arrange business meetings and provide meeting minutes for Regulatory Affairs and Marketing Authorization Holder activities.</li><li>Deliver administrative support, including office supplies, filing, business cards, postage, and phone coordination.</li><li>Create, process, and track purchase orders and invoices.</li><li>Coordinate domestic and international travel for Japan Regulatory Affairs members and global visitors.</li><li>Manage the Head of Japan Regulatory Affairs calendar, schedules, and expense reports.</li><li>Support internal communications and onboarding, hiring, and interview activities with Human Resources and Talent Acquisition.</li><li>Provide operational support to regulatory and safety teams in Japan.</li><li>You build trusted relationships while handling sensitive information with discretion.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Relevant degree or related discipline.</li><li>Minimum 5 years of experience as a Group Administrator or Administrative Coordinator in a global company.</li><li>5+ years of relevant experience, preferably within the pharmaceutical industry.</li><li>Ability to independently handle difficult inquiries using sound judgment.</li><li>Strong organizational skills with the ability to multitask and reprioritize work.</li><li>Ability to work under pressure while maintaining attention to detail.</li><li>Strong verbal, written, and interpersonal communication skills in Japanese and English.</li><li>Experience with Microsoft Word, Excel, PowerPoint, and Outlook.</li><li>Interest in helping establish and develop new local entities within global companies.</li><li>Team-oriented mindset and flexibility to support colleagues as needed.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 22 Aug 2026 02:56:17 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager - Statistical Programming, Central Services]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47788]]></requisitionid>
    <referencenumber><![CDATA[R47788]]></referencenumber>
    <apijobid><![CDATA[r47788]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47788/senior-manager-statistical-programming-central-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to expand our global footprint, our Global Capability Centers play a critical role in enabling scalable, high-quality operations and delivering impactful business services.</p><p>We are seeking a Senior Manager, Statistical Programming to join our Global Development function, supporting our Global Capability Center in Hyderabad in an on-site role. In this role, you will lead statistical programming activities across clinical programs, ensuring high-quality, compliant data outputs for regulatory submissions and integrated analyses, while collaborating with biostatisticians, data management, and cross-functional global teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>This position is office-based and will be on site at Regeneron’s Hyderabad office.</p><p><strong>Discover your role:</strong></p><ul><li><p>Serve as the technical lead for statistical programming across assigned clinical programs and regions.</p></li><li><p>Lead the development of integrated datasets and analysis outputs for clinical studies and regulatory submissions.</p></li><li><p>Coordinate the preparation and review of electronic submission packages (eCTD) for global regulatory bodies.</p></li><li><p>You bring strong analytical thinking and attention to detail, ensuring quality in every deliverable.</p></li><li><p>Drive process improvements and innovation to enhance efficiency and compliance across programming functions.</p></li><li><p>Partner with biostatisticians, data management, and cross-functional teams to deliver clinical reporting needs.</p></li><li><p>Mentor team members, building capability and fostering continuous learning across the function.</p></li><li><p>You thrive working across a global, matrixed organisation, building alignment with diverse team members.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>8+ years of experience in statistical programming within pharmaceutical, biotech, or clinical research, including leadership experience.</p></li><li><p>Proficiency in SAS programming with deep understanding of CDISC standards (SDTM, ADaM, Define-XML).</p></li><li><p>Proven experience supporting regulatory submissions to global bodies (FDA, EMA, PMDA).</p></li><li><p>Strong experience with clinical trial data and regulatory reporting processes.</p></li><li><p>Bachelor's degree in a relevant field.</p></li><li><p>Fluency in English with the ability to collaborate effectively across global teams.</p></li></ul><p><strong>Preferred:</strong></p><ul><li><p>Master's degree or higher in Statistics, Computer Science, Mathematics, Life Sciences, or related field.</p></li><li><p>Prior experience in global or Global Capability Center (GCC) environments.</p></li><li><p>Exposure to R or Python.</p></li><li><p>Experience with validation tools such as Pinnacle 21 (P21).</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 08:26:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manufacturing Support Technician]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48341]]></requisitionid>
    <referencenumber><![CDATA[R48341]]></referencenumber>
    <apijobid><![CDATA[r48341]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48341/manufacturing-support-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Manufacturing Support Technician</strong> to join our <strong>Manufacturing</strong><strong> </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & Where:</strong></p><ul><li><p>Location: Limerick</p></li><li><p>Shift: 24/7</p></li></ul></div><div><p><strong>What you’ll do:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as advised by Team Leads and Supervisors</p></li><li><p>Ensuring all associated documentation such as manufacturing batch records & logbooks are completed, accurate and verified in accordance with SOPs and cGMP Standards</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Maintaining housekeeping in designated area and adhering to the hygiene standards of the facility</p></li><li><p>Ensuring all required training is up to date and completed in a timely manner</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You will be working in a cleanroom where gowning is required</p></li><li><p>You enjoy working in a team that brings out the best in each other</p></li><li><p>You can adhere to the letter and spirit of policies and regulations</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Leaving Certificate qualification to include math's and a science or engineering subject as a minimum or equivalent qualification. Experience working shift in a GMP (Good Manufacturing Practice) environment/industry is preferred</p></li></ul><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IREADV #JOBSIEST #LI-Onsite #REGNIEEC #REGNIELSM</strong></p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€12.87 - €22.73]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Director Rare Disease Commercial EU4+UK Region]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50197]]></requisitionid>
    <referencenumber><![CDATA[R50197]]></referencenumber>
    <apijobid><![CDATA[r50197]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50197/sales-director-rare-disease-commercial-eu4plusuk-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sales Director Rare Disease</strong> to join our International Rare Disease team, supporting our EU4+UK region. In this role, you will lead a high-performing field organization and drive commercial execution across our rare disease portfolio while collaborating with cross-functional teams and regional leadership. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Location: Munich, Germany (multiple locations are being considered for this role) - Office based, Hybrid.</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead a sales team across EU4+UK to deliver company objectives.</p></li><li><p>Drive account targeting, segmentation, and multichannel customer engagement.</p></li><li><p>Set performance objectives and lead coaching, development, and succession planning.</p></li><li><p>Align incentive compensation plans with brand strategies and targets.</p></li><li><p>Partner with Commercial Operations on training, analytics, KPIs, Veeva CRM, and territory alignment.</p></li><li><p>Provide field insights on customer feedback, patient journey barriers, and competitive intelligence.</p></li><li><p>Partner with cross-functional team members to address market trends and dynamics.</p></li><li><p>You champion excellence, accountability, and patient-centricity across the organization.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree required.</p></li><li><p>Advanced degree in life sciences, pharmacy, medicine, or business strongly preferred.</p></li><li><p>Minimum 10 years’ experience in the pharmaceutical or biotechnology industry.</p></li><li><p>Minimum 3 years in a first-line field sales management role.</p></li><li><p>Proven success hiring, mentoring, developing, and retaining high-performing teams.</p></li><li><p>Experience in rare disease, specialized medicines, or gene therapy/ATMP commercialization preferred.</p></li><li><p>Ability to operate within sophisticated multi-stakeholder account environments.</p></li><li><p>Knowledge of market access and reimbursement frameworks across EU4+UK markets.</p></li><li><p>Ability to mentor teams on value-based and access-oriented payer engagement.</p></li><li><p>Experience with Veeva CRM, Salesforce effectiveness tools, data analytics, and digital promotion.</p></li><li><p>Proficiency in English and one additional European language highly desirable (French, German, Italian, or Spanish)</p></li><li><p>Knowledge of EFPIA and applicable national pharmaceutical industry codes.</p></li><li><p>Ability to travel 50% or more across EU4+UK and hold a valid driving licence.</p></li><li><p>Established KOL relationships in rare metabolic, musculoskeletal, or hearing loss areas are desirable.</p></li><li><p>Strong leadership, communication, and interpersonal skills in multicultural environments.</p></li></ul><p>(€110,250 - €183,750) </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Validation Engineer (Fill Finish)]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49821]]></requisitionid>
    <referencenumber><![CDATA[R49821]]></referencenumber>
    <apijobid><![CDATA[r49821]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49821/process-validation-engineer-fill-finish/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking a Process Controls & Validation Engineer to join our Process Sciences Drug Product Engineering department. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering and mathematical needs from the laboratory to the manufacturing floor. This non-lab based role focusing on fill finish operations provides technical support to manufacturing, quality and CMC Regulatory for manufacturing processes from technology transfer to post-commercial lifecycle management activities.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm </li></ul><p><strong>Discover your role:</strong></p><ul><li>Supports technology transfer, process control strategy, validation, and post-commercialization activities</li><li>Evaluates product and process risks throughout the process lifecycle</li><li>Analyzes data from development, characterization, and at-scale manufacturing</li><li>Collaborates with Manufacturing, QC, QA, and CMC Regulatory to support process lifecycle management</li><li>Authors protocols, reports, and technical documents based on process and product knowledge</li><li>Ensures SOPs, policies, and validation plans align with industry and regulatory standards (e.g., ICH guidelines)</li><li>Supports audits, inspections, and CMC regulatory submissions</li><li>Applies engineering principles to develop and execute process controls and validation strategies</li><li>Uses statistical and engineering methods to assess manufacturing process performance</li><li>Supports laboratory and manufacturing-scale studies</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li><p>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li></ul><p><strong>This role requires: </strong></p><ul><li>BS/BA in Engineering, Chemical Engineering, Biomedical Engineering preferred<ul><li>Process Controls & Validation Engineer: 2+ years of relevant experience</li><li>Sr. Process Controls & Validation Engineer: 5+ years of relevant experience</li><li>Level is determined based on qualifications relevant to the role</li></ul></li><li>A background in aseptic processing/ fill finish, technology transfer, drug product process development, or biopharmaceutical process validation is preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Program Head, Immunology]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48718]]></requisitionid>
    <referencenumber><![CDATA[R48718]]></referencenumber>
    <apijobid><![CDATA[r48718]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48718/executive-director-global-program-head-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Global Program Head to join our Immunology team, leading integrated program strategy for our Immunology portfolio from pre-IND nomination through BLA application. In this role, you will build and lead Strategic Program Teams, drive cross-functional program execution, and guide development of novel therapies for serious ophthalmic diseases while collaborating with research, clinical development, regulatory, commercial, and manufacturing partners across Regeneron.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY</li><li><strong>Work model/flexibility:</strong> 4 days a week on-site</li><li><strong>Travel: </strong>10% to relevant conferences/congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Build and lead Strategic Program Teams in developing long-term, end-to-end integrated program strategy</li><li>Drive scientific rigor and innovation into program development strategies</li><li>Orchestrate execution of program deliverables and governance interactions across functions</li><li>Hold sub-teams and their leads accountable for program strategy, plans, and timelines</li><li>Maintain financial oversight of program budgets and development costs</li><li>Identify and align key stakeholders across Regeneron and partner organizations throughout the program lifecycle</li><li>Oversee risk identification, assessment, and mitigation, making decisions informed by cross-functional input</li><li>Coach and support the professional development of Strategic Program Team members</li></ul><br><h3>This role requires:</h3><ul><li>MD, PhD, or PharmD</li><li>10-15 years of experience in broad drug development in Immunology or autoimmunity</li><li>Deep knowledge of the overall development of molecules for relevant disease areas</li><li>Expert knowledge of the competitive landscape and general regulatory requirements for drug approval</li><li>Experience or knowledge of biologics and alternative therapeutic modalities preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 20:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Development Program Management]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44512]]></requisitionid>
    <referencenumber><![CDATA[R44512]]></referencenumber>
    <apijobid><![CDATA[r44512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44512/manager-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Development Program Management to join our Development Program Management function, supporting drug development programs from preclinical through commercialization in a hybrid work model based in Warren, NJ or Tarrytown, NY. In this role, you will help drive strategic planning and execution of development program timelines, budgets, and goals while collaborating with cross-functional Strategic Program Team members across the organization. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><strong>Location:</strong> Warren, NJ or Tarrytown, NY</li><li><strong>Work model/flexibility:</strong> Onsite 4 days/week, 1 day remote</li></ul><p><strong>Discover your role:</strong></p><ul><li>Support subteam and functional area meetings, leading select working groups</li><li>Track deliverables, risks, and issues across assigned programs</li><li>Facilitate cross-functional alignment on key strategic documents</li><li>Manage project planning systems to keep programs on track</li><li>Communicate program status clearly to manager and stakeholders</li><li>Escalate risks and complex issues in a timely, appropriate manner</li><li>Build relationships and collaborate effectively across departments</li><li>Support resolution of team conflicts and roadblocks</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree and 5+ years of relevant project management experience</li><li>Experience in drug development/pharmaceutical industry preferred</li><li>Familiarity with cross-functional development team structures (e.g., Strategic Program Teams)</li><li>Demonstrated sound judgment and critical thinking</li><li>Ability to take feedback and setbacks constructively</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Quality Control (Microbiology)]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46658]]></requisitionid>
    <referencenumber><![CDATA[R46658]]></referencenumber>
    <apijobid><![CDATA[r46658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46658/supervisor-quality-control-microbiology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Supervisor, Quality Control</strong> to join our <strong>Quality Control (QC)</strong> team.</p><p>This position offers the opportunity to lead a team of quality control professionals supporting the manufacture and release of biopharmaceutical products for patients worldwide.</p><h3><strong>When & Where:</strong></h3><ul><li><p><strong>Location:</strong> Raheen, Limerick, Ireland</p></li><li><p>This is an onsite leadership role supporting Quality Control laboratory operations</p></li><li><p>The role involves supervising daily laboratory activities and supporting cross-functional business objectives</p></li></ul><h3><strong>What You'll Do:</strong></h3><ul><li><p>Lead and supervise QC personnel, allocating workload and monitoring team performance</p></li><li><p>Ensure laboratory activities comply with cGMP requirements, SOPs, and quality standards</p></li><li><p>Support investigations, troubleshooting activities, audits, and continuous improvement initiatives</p></li><li><p>Oversee documentation including SOPs, methods, protocols, reports, and training records</p></li><li><p>Manage employee development activities including scheduling, performance reviews, coaching, and training compliance</p></li></ul><h3><strong>The Environment and Physical Rhythms of This Role:</strong></h3><ul><li><p>Thrive in a fast-paced, GMP-regulated laboratory environment</p></li><li><p>Balance leadership responsibilities with operational priorities while maintaining a strong focus on quality and safety</p></li><li><p>Collaborate with cross-functional teams to support manufacturing and quality objectives</p></li><li><p>Foster a culture of continuous improvement, accountability, and employee development</p></li></ul><h3><strong>Let's Find Out if We're a Fit:</strong></h3><ul><li><p>Requires a BS/BA in Life Sciences or a related field; an MS degree is preferred</p></li><li><p>Requires 5+ years of relevant experience within the pharmaceutical, biotechnology, or related industry</p></li><li><p>Previous supervisory or people leadership experience is required</p></li><li><p>Experience working in a GMP-regulated environment with strong communication and problem-solving skills</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, CMC Regulatory Affairs]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50069]]></requisitionid>
    <referencenumber><![CDATA[R50069]]></referencenumber>
    <apijobid><![CDATA[r50069]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50069/manager-cmc-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, CMC Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan organization in a hybrid work mode. In this role, you will lead regulatory CMC activities across therapeutic areas while collaborating with Global Regulatory CMC, CMC Regulatory Science, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplement submissions.</li><li>Prepare Japanese application forms and support high-quality regulatory dossiers.</li><li>Drive regulatory decisions based on requirements while working across cross-functional teams.</li><li>Act as a local liaison with PMDA for CMC submissions and information requests.</li><li>Assess CMC change controls against regulatory filings to maintain compliance.</li><li>Review manufacturing processes and specifications against approved filings.</li><li>Participate in agency meetings and communicate regulatory positions and feedback.</li><li>You navigate ambiguity confidently and build effective partnerships across teams.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in a scientific discipline; Master's degree preferred.</li><li>Strong biopharmaceutical and regulatory Chemistry, Manufacturing and Controls (CMC) background.</li><li>15+ years of regulatory CMC experience, including health authority interactions, major submissions, and approvals in Japan.</li><li>Experience leading CTN, J-NDA, eCTD submissions, PCA, MCN, and PMDA responses.</li><li>Deep knowledge of Japanese regulatory requirements, guidance documents, and regulatory resources.</li><li>Experience managing submission timelines and delivering filings on schedule.</li><li>Ability to obtain and maintain Foreign Manufacturing Accreditation or Foreign Manufacture Registration.</li><li>High fluency in Japanese and English.</li><li>Ability to interpret regulations, communicate effectively, and think strategically.</li><li>Strong work ethic with proven collaboration across diverse teams.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Summer 2026 MD Intern, Internal Medicine]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43354]]></requisitionid>
    <referencenumber><![CDATA[R43354]]></referencenumber>
    <apijobid><![CDATA[r43354]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43354/summer-2026-md-intern-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>If you’re currently a medical school student interested in drug discovery and development, you may be a fit for an internship in our Internal Medicine Clinical Development Unit.</p><p><strong>In this role, a typical internship will include:</strong></p><ul><li><p>Achieving a general understanding of what happens in our global development organization</p></li><li><p>Completing a hands-on project that has an impact on the business</p></li><li><p>Engaging with Regeneron leadership</p></li><li><p>Collaborating with a specific hiring manager and other interns</p></li><li><p>Establishing connections with Regeneron’s diverse employee resource groups</p></li><li><p>Participating in professional development sessions</p></li><li><p>Showcasing the knowledge you gained through end of program presentation sessions</p></li><li><p>Getting paid for your hard work!</p></li></ul><p><strong>Internship Project Specifics:</strong></p><p>The summer intern will be placed on a project team in the Internal Medicine Clinical Development Unit at Regeneron. During this project the summer intern may visually and/or descriptively analyze clinical trial data from recent studies or databases. Disease areas that comprise the focus of the summer interns project may include: cardiovascular, pulmonary and/or immunological & inflammatory diseases.</p><p>The student will be trained on basic statistical modeling techniques using SAS JMP. The summer project may involve reviewing pharmacokinetic (PK) and pharmacodynamic (PD) data from clinical trials. Students will be trained on techniques for data cleaning, statistical analysis, and linear regression (univariate and multivariate). The student will work closely with the global program head, medical director and clinical pharmacology director during the project.</p><p>Additionally, students will be trained in Good Clinical Practice (GCP) standards for human clinical trials including relevant International Conference on Harmonization (ICH) and FDA Guidelines. The student will also attend relevant team meetings including: Strategic Project Team, Global Clinical Sub Team, Global Regulatory Sub Team and others as needed.</p><p>At the end of the summer internship period, the student will be expected to give a presentation/summary of their research experiences to an internal audience at Regeneron.</p><p>To be considered for this opportunity, you must be currently enrolled in medical school and returning to school the semester following the internship). A cumulative GPA of 3.0 is preferred. We want someone who is able to commit to 40 hours per week for a minimum of 6-8 weeks during a time-period from the end of May/ early June through August. The specific weeks of the internship are flexible and intended to accommodate the intern’s time out of school. Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community is also preferred.</p><p>Requirements:</p><ul><li><p>Medical student currently enrolled in an accredited US medical school (MD)</p></li><li><p>Must have completed at least the first-year basic science curriculum. Students who have completed the second year and beyond will also be considered but must have adequate time available during an elective or research rotation to be on site at Regeneron.</p></li><li><p>Familiarity with Microsoft Office tools (Word, Outlook, Powerpoint).</p></li><li><p>Prior research experience is preferred but not required. Understanding of biostatistics, experimental design and the scientific method is preferred. Experience with R studio, Python, SPSS, SAS or SAS JMP is a plus.</p></li><li><p>On site attendance at Regeneron offices in Tarrytown NY is expected 5 days per week</p></li></ul><p><strong><em>Please note our intern pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for Tarrytown, NY: $32.00-$40.70 per hour. </em></strong></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Category Management]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48239]]></requisitionid>
    <referencenumber><![CDATA[R48239]]></referencenumber>
    <apijobid><![CDATA[r48239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48239/associate-director-category-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking an Associate Director, Global Procurement Category Management to join our Global Procurement team, supporting our global categories in a hybrid work model. In this role, you will lead category management across global procurement categories while collaborating with team members, suppliers, Law, procurement colleagues and direct reports. This position offers the opportunity to help shape a procurement capability that acts as a competitive advantage to Regeneron.</p><p><strong>When & where:</strong></p><p>Hyderabad - (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead category management across a range of global categories.</p></li><li><p>Align category priorities with leaders, team members and suppliers.</p></li><li><p>Manage negotiations, supplier relationships and stakeholder engagement.</p></li><li><p>Drive cost savings, cash flow and efficiency improvements.</p></li><li><p>Negotiate contract terms with Law and business partners.</p></li><li><p>Use data and market insight to guide category decisions.</p></li><li><p>Coach procurement skills and career development across the team.</p></li><li><p>You bring clarity and integrity when driving change.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in a relevant field of study.</p></li><li><p>Progressive procurement experience, including Pharma or BioPharma experience.</p></li><li><p>Experience managing global category processes and suppliers.</p></li><li><p>S-u+ccess leading cross-functional teams across sourcing, negotiations and contracting.</p></li><li><p>Experience managing supply market evaluation using market intelligence, risk, compliance and financial assessment tools.</p></li><li><p>Working knowledge of sourcing, contracting, ERP and eRFx systems preferred, including Oracle, Zycus or Ariba.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - DETROIT North, MI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48047]]></requisitionid>
    <referencenumber><![CDATA[R48047]]></referencenumber>
    <apijobid><![CDATA[r48047]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48047/medical-account-specialist-ii-neurology-detroit-north-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Detroit]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Detroit North (Metro), Michigan </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHOENIX S, AZ]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48072]]></requisitionid>
    <referencenumber><![CDATA[R48072]]></referencenumber>
    <apijobid><![CDATA[r48072]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48072/medical-account-specialist-ii-neurology-phoenix-s-az/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Pheonix (South Metro), AZ</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LONG ISLAND, NY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48008]]></requisitionid>
    <referencenumber><![CDATA[R48008]]></referencenumber>
    <apijobid><![CDATA[r48008]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48008/medical-account-specialist-ii-neurology-long-island-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Garden City]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Long Island (Metro), NY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager - Delivery & Operations Product Lead - Business Process Management]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47515]]></requisitionid>
    <referencenumber><![CDATA[R47515]]></referencenumber>
    <apijobid><![CDATA[r47515]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47515/senior-product-manager-delivery-operations-product-lead-business-process-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Global Development Information Technology (GD IT) is seeking an outstanding Senior Product Manager to lead product delivery for innovative Business Process Management (BPM) applications that transform the way clinical studies are developed, planned, and assessed. As the Product Lead on the Enabling Technologies team, you will drive low-code BPM (Appian) and generative/agentic AI solutions that streamline study design, feasibility, and downstream planning.</p><p>You will be responsible for the full product lifecycle—roadmap, design, build, testing, launch, and operations, while ensuring alignment with business goals, regulatory standards, and data-privacy requirements. Your blend of clinical process expertise, agile leadership, and technical savviness will be critical to delivering measurable value across Global Development.</p><p><strong>In this role, a typical day might include the following:</strong> <br>- Leading stand-ups, grooming backlogs, and approving Appian user stories for study-design workflows <br>- Facilitating workshops with clinical stakeholders to map current vs. future processes and prioritize AI-enabled improvements <br>- Reviewing solution architecture to ensure secure, scalable integrations with data, analytics, and LLM-based services <br>- Supervise sprint progress, mitigating risks, and updating program leadership on timelines, budget, and return of investment.<br>- Monitoring platform performance and adoption, then identifying automation or reporting improvements <br>- Preparing and presenting demos or governance materials for steering committees and change-control boards </p><p><strong>This job might be for you if you: </strong><br>- Combine deep knowledge of clinical development processes with hands-on product and low-code platform expertise <br>- Enjoy partnering with clinical, data, and architecture leaders, to translate complex operational problems into clear, innovative digital solutions and roadmaps <br>- Excel at stakeholder management, influencing cross-functional teams without direct authority <br>- Thrive in agile environments, balancing short-term results with long-term strategy <br>- Enjoy working with data science teams to embed RAG, MCP, or LLM capabilities into business workflows <br>- Keep a “get-it-done” mentality, balancing multiple high-impact initiatives while maintaining quality </p><p><strong>In order to be considered for this role, you must have: </strong><br>- BS/BA with 8–10 years proven experience (or MS/MBA with 6+ years as an equivalent), including 3 years in enterprise SaaS and 1+ year delivering generative/agentic AI solutions <br>- Shown success implementing Appian or similar BPM platforms for clinical or regulated environments <br>- Proven track record driving process optimization, agile delivery, and cross-system integrations in Global Development</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -  CINCINNATI, OH]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48024]]></requisitionid>
    <referencenumber><![CDATA[R48024]]></referencenumber>
    <apijobid><![CDATA[r48024]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48024/medical-account-specialist-ii-neurology-cincinnati-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cincinnati]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Cincinnati (Metro), OH</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - COLUMBIA, SC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48019]]></requisitionid>
    <referencenumber><![CDATA[R48019]]></referencenumber>
    <apijobid><![CDATA[r48019]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48019/medical-account-specialist-ii-neurology-columbia-sc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbia]]></city>
    <state><![CDATA[South Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Columbia (Metro), SC</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager HR Business Partner]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48083]]></requisitionid>
    <referencenumber><![CDATA[R48083]]></referencenumber>
    <apijobid><![CDATA[r48083]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48083/senior-manager-hr-business-partner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, HR Business Partner to join our Human Resources function, supporting our France, Canada, and Belgium operations in a hybrid work mode. In this role, you will deliver the full spectrum of HR activities supporting the international Commercial business while collaborating with HR Centers of Excellence, business leaders, and the Legal team. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><br><br><h3><strong>When & where:</strong></h3><br><p>Paris, France; Hybrid</p><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Deliver full spectrum HR activities across employee lifecycle</li><li>Manage employee relations cases and regulatory compliance requirements</li><li>Partner with business leaders to align HR priorities and solutions</li><li>Lead labour relations engagement with works council representatives</li><li>Support talent acquisition, onboarding, and talent review processes</li><li>Drive organisational development initiatives with leadership teams</li><li>Navigate complexity and balance operational and strategic priorities</li><li>Build constructive relationships with employee representatives and stakeholders</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree in HR or related discipline, or equivalent experience</li><li>Minimum 8 years’ HR experience including international commercial support</li><li>Fluency in French and English languages</li><li>Demonstrated expertise in labour relations and works council engagement</li><li>Experience across full HR lifecycle from administration to strategic partnering</li><li>Strong data literacy and experience with HR systems and Microsoft tools</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€71,925.00 - €119,875.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lab Equipment Maintenance Technician III (2nd Shift: 3:00PM-11:30PM)]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41868]]></requisitionid>
    <referencenumber><![CDATA[R41868]]></referencenumber>
    <apijobid><![CDATA[r41868]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41868/lab-equipment-maintenance-technician-iii-2nd-shift-300pm-1130pm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Laboratory Equipment Maintenance Technician III to join our Equipment Services team supporting scientific operations across laboratory and vivarium environments. In this role, you will install, maintain, calibrate, and repair laboratory and vivarium equipment to ensure safe, reliable, and compliant operations that directly support research innovation and high-quality animal care.</p><p><strong>A Typical Day Might Include:</strong></p><ul><li>Conducting preventive and corrective maintenance on key laboratory and vivarium equipment, including:<ul><li>CO₂ incubators and biosafety cabinets</li><li>Cryogenic liquid nitrogen freezers</li><li>Autoclaves & sterilizers</li><li>Vivarium industrial tunnel and cage washers</li><li>Clean steam generation systems</li><li>RO/DI laboratory water purification system</li></ul></li><li>Troubleshooting electromechanical, control-system, and monitoring device issues to minimize equipment downtime</li><li>Responding to equipment and site emergencies, including 24/7 support</li><li>Responding to environmental and equipment alarms from Rees, Dickson, Watchdog EX, and related monitoring systems</li><li>Maintaining accurate electronic work order documentation, calibration records, and asset compliance data</li><li>Supporting audit and inspection readiness for AAALAC, IACUC, and internal compliance activities</li><li>Partnering closely with researchers, veterinarians, and animal care specialists to ensure equipment performance meets scientific study requirements</li></ul><p><strong>This Role Might Be for You If You:</strong></p><ul><li>Possess strong mechanical, electrical, and controls troubleshooting abilities</li><li>Communicate clearly and professionally with cross-functional partners</li><li>Demonstrate excellent attention to detail in regulated documentation</li><li>Stay calm and organized when prioritizing urgent research-impacting needs</li><li>Enjoy working in specialized laboratory areas with strict safety and cleanliness standards</li></ul><p><strong>In Order To Be Considered, You Must Have:</strong></p><ul><li>High school diploma or equivalent and 4+ years relevant technical experience in laboratory, or industrial equipment maintenance<ul><li>Trade school in a related field (Engineering Technology, Biomedical Technology, etc.) is a plus</li></ul></li><li>Hands-on experience with:<ul><li>Motors, pumps, valves, and sensors</li><li>VFDs and PLC-controlled systems</li><li>24 VDC, 3-Phase 208V, and 480V</li><li>Technical schematics and electrical diagrams</li></ul></li><li>Ability to lift and/or move equipment up to 100 lbs.</li><li>Willingness to work in vivarium research facilities as required (around animals)</li><li>Valid driver’s license recognized by the State of New York</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$29.81 - $46.63]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Direct and FC&L Procurement]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48234]]></requisitionid>
    <referencenumber><![CDATA[R48234]]></referencenumber>
    <apijobid><![CDATA[r48234]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48234/manager-direct-and-fcl-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Direct Materials Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will drive category strategy, sourcing, and supplier performance for direct materials while collaborating with cross-functional partners and global procurement colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Drive the definition and implementation of global direct material category strategies aligned to regional and global business needs</p></li><li><p>Partner with collaborators to manage category priorities, sourcing decisions, and procurement activities across direct materials</p></li><li><p>Lead negotiations, contracting, and supplier management to deliver cost savings, cash flow improvements, and operational efficiencies</p></li><li><p>Ensure category activities align with GxP and applicable regulatory standards</p></li><li><p>Collaborate with Legal to negotiate contract terms and conditions aligned to business requirements</p></li><li><p>Use market intelligence, supplier insights, and data analytics to inform decision-making and improve category performance</p></li><li><p>Contribute to organizational decisions and initiatives that shape global procurement capabilities and category outcomes</p></li><li><p>You operate effectively in a matrixed, global environment and build strong, trusted relationships with internal and external partners.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive experience in procurement, including Pharma/Biopharma.</p></li><li><p>Proven experience managing category strategies, sourcing, contracting, and supplier relationships across direct materials or related categories.</p></li><li><p>Strong negotiation capability with understanding of cost structures, rates, and supply market dynamics.</p></li><li><p>Demonstrated success working with cross-functional teams to deliver results across procurement activities.</p></li><li><p>Experience supporting supplier evaluation processes using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Knowledge of global procurement processes and operating models within the biopharmaceutical industry.</p></li><li><p>Ability to demonstrate data and analytics to drive category decisions and project outcomes</p></li><li><p>Experience managing or coaching professional-level employees preferred.</p></li><li><p>Working knowledge of sourcing and contracting tools, ERP systems, and eRFx platforms (e.g., Oracle, Zycus, Ariba) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint)</p></li><li><p>Strong communication, collaboration, and collaborator management skills with the ability to work effectively in ambiguous environments.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Southeast)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48131]]></requisitionid>
    <referencenumber><![CDATA[R48131]]></referencenumber>
    <apijobid><![CDATA[r48131]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48131/field-reimbursement-manager-neurology-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Atlanta]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Atlanta (Metro), GA Jacksonville (Metro), AL Fort Lauderdale, (Metro) FL, Miami (Metro), FL, Tampa (Metro), FL, Saint Petersburg (Metro), FL, Birmingham (Metro), AL, Mobile (Metro), AL</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48306]]></requisitionid>
    <referencenumber><![CDATA[R48306]]></referencenumber>
    <apijobid><![CDATA[r48306]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48306/specialist-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Specialist, External Data Acquisition and Delivery to join our Clinical Data Management team. In this role, you will manage non-Case Report Form data across assigned studies or Clinical Development Units while collaborating with external data vendors, CRO partners, Clinical Data Management and cross-functional stakeholders. This position offers the opportunity to support data integrity, improve external data delivery and strengthen compliant study execution.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Manage end-to-end non-Case Report Form data delivery.</li><li>Develop low-complexity Data Transfer Specifications for assigned studies.</li><li>Reconcile external vendor data with clinical database outputs.</li><li>Track specification status across data types and programmes.</li><li>Support data structure issue resolution and change requests.</li><li>Maintain documentation, audit trails and inspection readiness standards.</li><li>You collaborate across teams to resolve data discrepancies.</li><li>You support continuous improvement in external data processes.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in Science, Health, Mathematics, Engineering, Computational or related field.</li><li>2+ years in external clinical data acquisition or management.</li><li>Experience managing clinical data types such as biomarker, eCOA, imaging, ECG, PK, genomics and laboratory data.</li><li>Knowledge of 21 CFR Part 11, ICH-GCP and CDISC standards.</li><li>Experience extracting data into SAS, CSV and XML formats.</li><li>Knowledge of EDC platforms and external data reconciliation processes.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences]]></title>
    <date><![CDATA[Sun, 12 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47082]]></requisitionid>
    <referencenumber><![CDATA[R47082]]></referencenumber>
    <apijobid><![CDATA[r47082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47082/medical-director-clinical-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Clinical Sciences team, supporting our Japan clinical development programs in a hybrid capacity. In this role, you will support the scientific and clinical aspects of assigned clinical development programs while collaborating with the Global Clinical Sub Team and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Japan Local Country Office</li><li>Hybrid work model</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Support the Japan Clinical Development Lead in clinical components of assigned development programs and contribute to the Global Clinical Sub Team</li><li>Adapt clinical trial protocols, amendments, CRFs, IRB applications, informed consent forms, and recruitment materials for Japan-specific requirements</li><li>Provide clinical input for regulatory documents including CTN submissions, Investigator Brochures, J-NDA/J-CTD submissions, and PMDA responses</li><li>Review clinical data and prepare study reports, abstracts, manuscripts, and presentations</li><li>Assess clinical feasibility with local medical needs for Japan's participation in global studies and provide enrollment input</li><li>Build KOL and investigator site relationships with Clinical Trial Liaisons, Clinical Operations, and Medical Affairs teams</li><li>You will stay current on scientific progress in assigned therapeutic areas and represent the company at conferences</li><li>Collaborate with regulatory affairs, project management, clinical operations, medical affairs, and Global Patient Safety teams</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>MD or MD/PhD degree</li><li>Minimum 5 years pharmaceutical industry experience with at least 3 years in clinical development</li><li>Experience contributing to regulatory filings and clinical documents, particularly CTN and J-NDA/J-CTD submissions</li><li>Clinical trial design expertise across Phase I, II, and III studies</li><li>Experience with protocol design, clinical data review, and medical monitoring activities</li><li>Business-level English proficiency with strong communication skills in Japanese and English</li><li>Strong analytical, problem-solving, and influencing skills</li><li>Ability to work effectively within matrix environments and cross-functional teams</li><li>Strong presentation and medical writing skills</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development IT & Digital]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45997]]></requisitionid>
    <referencenumber><![CDATA[R45997]]></referencenumber>
    <apijobid><![CDATA[r45997]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45997/senior-manager-global-development-it-digital/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong> Tokyo, Japan</p><p>We are seeking a dedicated and innovative <strong>Global Development IT & Digital Manager</strong> to join our team in Tokyo. This pivotal role supports our Global Clinical Development, Patient Safety, Regulatory Affairs, and Medical Affairs organizations by leveraging IT solutions to drive high business value. As a trusted partner, you will collaborate across diverse teams, blending technical expertise with a deep understanding of pharmaceutical industry processes to deliver impactful results.</p><p>If you are passionate about IT, thrive on solving complex challenges, and are eager to make a meaningful difference in the pharmaceutical space, this role offers an exciting opportunity to grow and lead in a globally connected environment.</p><p><strong>A Typical Day:</strong><br>In this role, you will:</p><ul><li>Develop and implement IT action plans aligned with global and local business strategies.</li><li>Collaborate with local business units to understand and address goals, challenges, and regulatory requirements.</li><li>Manage IT projects and products, ensuring compliance with GxP regulations.</li><li>Promote IT-based business improvements using automation, data utilization, and cloud technologies.</li><li>Drive digital transformation initiatives leveraging AI, cloud, and data analytics.</li><li>Facilitate meetings and presentations in business-level English while coordinating with international teams.</li><li>Build and maintain a stable IT infrastructure, ensuring operational excellence.</li><li>Utilize development methodologies (agile, waterfall, hybrid) tailored to business needs.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You enjoy connecting IT with business needs and bridging different viewpoints through structured thinking and effective communication.</li><li>You have a curious and open mindset toward understanding multiple business domains and perspectives.</li><li>You thrive in collaborative environments and build trusted relationships with stakeholders.</li><li>You excel at problem-solving and are motivated by continuous improvement.</li><li>You are detail-oriented and capable of translating complex ideas into clear, actionable plans.</li><li>You are proficient in business-level English and skilled in facilitating conferences and delivering impactful presentations.</li></ul><p><strong>To Be Considered:</strong><br>You must have:</p><ul><li>Over five years of experience in the pharmaceutical industry, specifically in IT for development and medical departments.</li><li>A solid understanding of operational processes in drug development, clinical trials, and medical affairs.</li><li>Proven experience as an IT business analyst, IT project manager, or IT product manager.</li><li>Knowledge of GxP, regulatory compliance, and Computer System Validation (CSV).</li><li>Basic programming knowledge and familiarity with IT infrastructure (hardware, software, databases, networks, cloud).</li><li>Experience with agile and waterfall development methodologies.</li></ul><p>Preferred qualifications include:</p><ul><li>Execution and stakeholder management skills demonstrated through collaboration and accountability.</li><li>A constructive, positive approach to challenges and problem-solving.</li></ul><p>Join us to shape the future of IT-driven innovation in the pharmaceutical industry. Apply today to become part of a team that values curiosity, collaboration, and excellence.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst – Science Data Portal]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48904]]></requisitionid>
    <referencenumber><![CDATA[R48904]]></referencenumber>
    <apijobid><![CDATA[r48904]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48904/principal-business-analyst-science-data-portal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Principal Business Analyst Science Data Portal (SDP), will work collaboratively with Research & Preclinical Development scientists as well as other IT stakeholders, to understand and document scientific drug discovery data challenges and translate these into requirements for the development of data and technology solutions that help scientists to leverage their data for broader/deeper insights. Artificial Intelligence will be a large part of this process and of the solution landscape moving forward. </p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Translate business strategies, goals, and objectives into clear requirements; document problem statements with quantifiable business value </p></li></ul><ul><li><p>Document “as is” and “to be” business processes; identify, verify, and document functional and non-functional requirements using standard methodologies and tools </p></li></ul><ul><li><p>Map information system connections and data flows between systems; identify data elements and provide data mapping and data dictionaries </p></li></ul><ul><li><p>Write SQL statements to investigate data; understand data lake principles and different database types </p></li></ul><ul><li><p>Maintain and prioritize the backlog of requests; ensure the development team has absolute clarity on requirements; manage business stakeholder expectations </p></li></ul><ul><li><p>Work with scientists and laboratory personnel to understand business processes and suggest improvements; partner with research scientists and technical teams to define system goals and requirements </p></li></ul><ul><li><p>Pursue data quality issues to root cause; collaborate with business and IT partners to address issues intelligently </p></li></ul><ul><li><p>Handle a variety of tasks, effectively solve problems with complex variables, and shift priorities as needed in a fast-paced research environment </p></li></ul><ul><li><p>Work alongside stakeholders to test solutions for accuracy and consistency of results </p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Master’s degree in a life science with experience in computer science or information technology.</p></li><li><p>7+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment. </p></li><li><p> Previous experience in the biotechnology and/or pharmaceutical industry is required. We need someone who is adept at using a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, data and process modeling frameworks, data visualization tools such as Spotfire or Tableau) in order to perform business analysis, elicit and document requirements, map data flows, model data solutions, and drive data quality improvements in a research-focused environment.</p></li><li><p>Previous experience with drug discovery program management, biological laboratory techniques, bioinformatics methods, relational database concepts, databricks, Large Language Models, IT project and software development lifecycle methodologies, and managing or leading software development projects is preferred. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Biotech Production - Downstream (Shift)]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49287]]></requisitionid>
    <referencenumber><![CDATA[R49287]]></referencenumber>
    <apijobid><![CDATA[r49287]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49287/supervisor-biotech-production-downstream-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Supervisor Biotech Production</strong> to join our <strong>Manufacturing </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li><li><p>Other information: You will be required to work shift (days, nights, weekends)</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Supervising commercial scale manufacturing of recombinant proteins according to approved protocols, regulation, and schedule</p></li><li><p>Supervising a team responsible for the manufacture of bulk drug substance in a cGMP regulatory environment</p></li><li><p>Ensuring that the highest safety and housekeeping standards are maintained</p></li><li><p>Supervising all aspects of respective areas of operations</p></li><li><p>Reviewing and edits batch records in accordance with cGMP standards</p></li><li><p>Ensuring availability of production batch records for upcoming lots</p></li><li><p>Scheduling duties and batch tasks based on master production schedule</p></li><li><p>Ensuring equipment readiness and coordinates regular equipment maintenance and calibrations; troubleshoots equipment</p></li><li><p>Performing cGMP audits of production area</p></li><li><p>Performing people management duties including time sheet submissions, scheduling of vacations, personnel development, disciplinary actions, hiring, terminations, and performance evaluations</p></li><li><p>Scheduling individual and ongoing training</p></li><li><p>Interfaces with other departments, such as Facilities, Process Development, Process Analytical Sciences, Regulatory, Quality Assurance and Quality Control</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You possess logical troubleshooting and problem-solving skills</p></li><li><p>You have excellent analytical, written and oral communication skills</p></li><li><p>You demonstrate an ability to work with and supervise a successful team</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>Requires BS/BA in Life Sciences or related field with 5+ years of relevant cGMP manufacturing experience and some previous supervisory/leadership experience. Will substitute relevant experience in lieu of educational requirement.</p></li></ul><h3>Thrive today. Grow tomorrow.</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Study Associate Manager]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48805]]></requisitionid>
    <referencenumber><![CDATA[R48805]]></referencenumber>
    <apijobid><![CDATA[r48805]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48805/clinical-study-associate-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Associate Manager to join our Clinical Trial management team. In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial delivery, applying to both internally sourced studies and studies out-sourced to CROs, while collaborating with the study team internally and externally with vendors such as CROs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Armonk, NY, Warren, NJ, Cambridge, MA</p></li><li><p>Travel percentage: May require 25% travel</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with global study plans, and may contribute to global planning and management of the study</p></li><li><p>Contributes to risk assessment and helps identify risk mitigation strategies, and supports feasibility assessment to select relevant regions and countries</p></li><li><p>Oversees and provides input to the development of study specific documentation (e.g., CRF, data management plan, monitoring plan, monitoring oversight plan) and reviews site level informed consents and other patient-facing study start-up materials</p></li><li><p>Oversees setting up and maintenance of study systems including CTMS and TMF, and contributes to investigator meeting preparation and execution</p></li><li><p>Oversees engagement, contracting and management of required vendors for the study, and oversees and provides input to study drug and clinical supplies' forecasting, drug accountability and drug reconciliation</p></li><li><p>Provides regular status reports to collaborators as requested by the Clinical Study Lead, and contributes to development of and oversees implementation of recruitment and retention strategies</p></li><li><p>Monitors recruitment and retention, and monitors progress for site activation and monitoring visits</p></li><li><p>Supports data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites, and escalates data flow and data quality issues to Clinical Study Lead</p></li><li><p>Oversees the execution of the specific clinical study deliverables against planned timelines, escalates issues related to timelines or budget to Clinical Study Lead, and supports accurate budget management and scope changes</p></li><li><p>Contributes to clinical project audit and inspection readiness throughout the study lifecycle, and supports internal and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages aspects of study close-out activities including database lock, reconciliation of vendor contract, study budget, TMF and study drug accountability, may mentor clinical trial management staff, and may be assigned unmasked tasks for studies (e.g., unmasked TMF management, unmasked data review, IVRS point of contact)</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's Degree and 4+ years of relevant industry experience</p></li><li><p>A data driven approach to executing and problem solving, and attention to details for the ability to deliver on specific study activities</p></li><li><p>Technical proficiency in trial management systems and MS applications including Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, TMF</p></li><li><p>Budget awareness with the ability to participate in various aspects of budget management</p></li><li><p>Familiarity with medical terms, and vendor management experience</p></li><li><p>Experience in clinical trial operations including experience developing key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Applied AI, Advanced Informatics]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48861]]></requisitionid>
    <referencenumber><![CDATA[R48861]]></referencenumber>
    <apijobid><![CDATA[r48861]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48861/manager-applied-ai-advanced-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Applied AI to join our Advanced Informatics team, supporting health data systems and analytical pipelines across the organization. In this role, you will design and validate applied AI/ML solutions against complex health data and clinical ground truth, while collaborating with senior applied AI leaders, clinical informaticists, data engineers, and production ML engineers to build reusable analytical capabilities the broader informatics team depends on.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Tarrytown, NY, Armonk, NY, or Warren, NJ</p><p><strong>Discover your role:</strong><br>• Frame clinical and business informatics challenges into well-scoped AI/ML problem statements with clear success criteria<br>• Design and build ML pipelines — data ingestion, feature engineering, training, and evaluation — alongside production engineering<br>• Run experiments, benchmarks, and ablation studies to validate model performance and guide modeling decisions<br>• Partner across clinical informatics, data engineering, and ML engineering to bring models into real informatics workflows<br>• Track advances in foundation models, LLMs, and retrieval-augmented generation, and apply them to biomedical and health data<br>• Document research findings and contribute to internal reports, publications, or conference presentations<br>• Explain model behavior, limitations, and performance in terms both technical and non-technical team members can act on</p><p><strong>This role requires:</strong><br>• Bachelor's degree in Computer Science, Machine Learning, Data Science, Biomedical Informatics, Statistics, or related field; Master's or Ph.D. strongly preferred with 4–6 years + of progressive experience in applied AI/ML, with demonstrated ability to independently develop and evaluate models (Ph.D. graduates with relevant research experience may be considered) <br>• Solid grounding in supervised, unsupervised, and self-supervised learning, deep neural networks, and modern ML frameworks (PyTorch, TensorFlow, or equivalent)<br>• Strong Python skills across the scientific ML stack (scikit-learn, HuggingFace Transformers, pandas, NumPy)<br>• Experience designing and evaluating NLP or multimodal models, including LLM fine-tuning or prompt engineering<br>• Comfort with experiment tracking, model versioning, and reproducible research practices (MLflow, W&B, DVC, or similar)<br>• Familiarity with cloud-based ML infrastructure (AWS SageMaker, GCP Vertex AI, Azure ML, or equivalent).<br>• Experience with health or life sciences data — EHR/EMR, claims, clinical notes, genomic, or imaging data<br>• Familiarity with medical terminologies and ontologies (SNOMED CT, ICD-10/11, LOINC, RxNorm, OMOP CDM)<br>• Published work or open-source contributions in applied ML, NLP, or computational biomedicine<br>• Experience with MLOps, CI/CD for ML, or model observability in production<br>• Familiarity with federated learning, privacy-preserving ML, or regulated-environment data use agreements</p><p>#AAI</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47668]]></requisitionid>
    <referencenumber><![CDATA[R47668]]></referencenumber>
    <apijobid><![CDATA[r47668]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47668/principal-business-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Job Description</p></div><div><p><strong>Build our future together:</strong></p><p>Regeneron is looking for an outstanding Principal Business Analyst to drive consistency across the Global Development (GD) IT team, and be a member of the GD Digital Transformation Program. This individual will work closely with GD IT leadership, and GD partners such as Business Process Owners, Subject Matter Experts, Training and Process & Procedures teams members in support of the overall Program and specific use cases.</p><p><strong>Where: </strong>Based at our Warren, NJ location</p><p><strong>When: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p></div><ul><li><p>Collaborate with GD IT Leadership to support the GD Digital Transformation Program, including overall program management.</p></li><li><p>Support the delivery of a GD Digital Transformation Program “use case” (new digital solution to improved efficiency and ways of working across GD)</p></li><li><p>Develop frameworks to gather accurate, measurable requirements that dictate project outcomes</p></li><li><p>Build flexible processes and frameworks in support of traditional (e.g., waterfall) and hybrid (e.g., agile) delivery methods</p></li><li><p>Collect GD IT operational metrics, analyze, identify & develop action plans for areas of improvement</p></li><li><p>Introducing new insights, approaches, solutions and technologies for GD IT</p></li><li><p>Collaborating with GD IT agile Delivery & Operations and Data Enablement leads to ensure that solutions are appropriately planned, accomplished, and improved upon</p></li><li><p>Provide direction on projects and technology products to optimally manage user expectations, timelines, budget and overall efforts for value realization</p></li><li><p>Work collaboratively with GD functions, Corporate IT, and other relevant functions in the management of enterprise systems, including development and adherence to standards and governance</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Bachelor's degree in a related field BS/BA Degree </p></li><li><p>7+ years of relevant work experience</p></li><li><p>Knowledge of pharmaceutical Global Development business capabilities, processes, applications, and key trends in the industry</p></li><li><p>Experience in one or more of the following Clinical Development functions in support of IT: Medical Affairs, Regulatory Affairs, Global Patient Safety, Clinical Operations, Biostatistics & Data Management, Clinical Quality, etc.</p></li><li><p>Robust business acumen and analytical expertise, to consistently drive operational enhancements and work practices' optimization</p></li><li><p>Self-drive & ability to work in ambiguity, with minimal oversight</p></li><li><p>Basic to intermediate proficiency in AI tools (e.g. CoPilot), and building AI agents</p></li><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders</p></li><li><p>Experience with Waterfall/Hybrid/Agile project methodologies and associated tools (e.g., Jira, Confluence)</p></li><li><p>Strong track record of technology project, stakeholder, and budget management </p></li><li><p>Ability to coordinate, influence and empower diverse teams to achieve goals</p></li><li><p>Experience working within and knowledge of GXP/GCP and regulatory ICH 6 guidelines</p></li><li><p>Expertise with MS Office Suite</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Precision Medicine Operations]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49775]]></requisitionid>
    <referencenumber><![CDATA[R49775]]></referencenumber>
    <apijobid><![CDATA[r49775]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49775/manager-precision-medicine-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build Our Future Together</strong></p></div><div><div><div><div><div><div><div><div><div><p>The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology. In this role, you will be a key driver of precision medicine operational execution partnering with Precision Medicine Strategy Lead (PMSL), clinical study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL), Clinical Laboratory Study Manager (CLSM), and Clinical Laboratory Project Management (CLPM) groups to deliver high-quality samples and data. Through strong cross functional collaboration and operational excellence, you will help ensure biomarker and non-biomarker strategies are executed seamlessly, enabling the translation of innovative science to medicines for patients.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Dublin, Ireland</p></li><li><p>Work model/flexibility: 3 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Works with project manager and set-up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics</p></li><li><p>Monitor’s acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensure compliance with ICF permissions</p></li><li><p>Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing </p></li><li><p>Work closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries.</p></li><li><p>Oversees Study start up, closeout and overall life-cycle activities for assigned studies at central lab/specialty labs to support all samples and testing</p></li><li><p>Provides input on sample-related section in clinical trial-related (e.g. protocols and ICF) and other supporting documents</p></li><li><p>Works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials.</p></li><li><p>Enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor's degree with a minimum of 8 years of pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams.</p></li><li><p>Minimum of 5 years' experience with Clinical Trials, focus on clinical sample collection</p></li><li><p>Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested.</p></li><li><p>Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required.</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€74,000.00 - €120,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  MILWAUKEE, MADISON, WI]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48951]]></requisitionid>
    <referencenumber><![CDATA[R48951]]></referencenumber>
    <apijobid><![CDATA[r48951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48951/medical-account-specialist-ii-hematology-milwaukee-madison-wi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madison]]></city>
    <state><![CDATA[Wisconsin]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Madison & Milwaukee, WI</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-Philadelphia, PA]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49760]]></requisitionid>
    <referencenumber><![CDATA[R49760]]></referencenumber>
    <apijobid><![CDATA[r49760]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49760/medical-account-specialist-ii-philadelphia-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Philadelphia, PA</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred)</p></li><li><p>We are also seeking Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions</p></li><li><p>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks</p></li><li><p>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace</p></li><li><p>You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization</p></li><li><p>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Must have ability to travel and cover large geography territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I - Analytics Automation Development]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47917]]></requisitionid>
    <referencenumber><![CDATA[R47917]]></referencenumber>
    <apijobid><![CDATA[r47917]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47917/process-development-engineer-i-analytics-automation-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an energetic <strong>Process Development Engineer I</strong> to join our Preclinical Manufacturing and Process Development (PMPD) department, supporting research and development efforts in an on-site capacity. In this role, you will execute experiments with minimal supervision, developing and validating automated methods for platform analytical assays and routine sample characterization, while planning, programming, and maintaining automated systems in a fast-paced, collaborative environment.</p><p>This position offers the opportunity to contribute to additive manufacturing and data automation initiatives within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><strong>Shift Requirements:</strong> Full-time, standard business hours in a fast-paced laboratory environment</li><li><strong>Location:</strong> On-site</li><li><strong>Flexibility & travel:</strong> Minimal to no travel; consistent on-site presence required to support lab operations</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Develop, implement, and troubleshoot automated workflows on automated systems including Hamilton Robotics, Biosero, and HighRes</li><li>Increase efficiency and throughput while improving data quality through process and tooling innovations</li><li>Provide hands-on support for operation, troubleshooting, and maintenance of automated systems and peripheral devices</li><li>Evaluate and recommend new technologies; assess their impact on existing workflows</li><li>Contribute to programming projects that support automated data initiatives</li><li>Ensure GLP-compliant work and documentation for automated assay verification; maintain a clean, safe, and compliant laboratory</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is an on-site, hands-on laboratory role requiring a good understanding of core laboratory techniques (e.g., pipetting) and the ability to execute experiments with minimal supervision</li><li>The role involves regular hands-on operation, troubleshooting, and maintenance of automated liquid-handling and lab-automation systems</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><ul></ul><h3><strong>Must-haves:</strong></h3><ul><li>BS in an<strong> </strong>Engineering discipline with 3+ years of experience, or MS with 0–3 years of experience</li><li>Strong lab automation experience, including programming liquid handlers (e.g., Hamilton) and integrating work cells with scheduling software (e.g., Green Button Go, Cellario)</li><li>Self-starter who is highly organized, a good problem solver, and detail-oriented</li><li>Strong analytical and written/oral communication skills</li><li>Team-oriented, with experience working in a diverse and multicultural environment</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Experience developing and validating automated methods for platform analytical assays and routine sample characterization</li><li>Experience planning, programming, and maintaining automated systems</li><li>Interest or experience contributing to additive manufacturing and data automation initiatives</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Patient Advocacy]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48174]]></requisitionid>
    <referencenumber><![CDATA[R48174]]></referencenumber>
    <apijobid><![CDATA[r48174]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48174/senior-director-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're looking for a Senior Director, Patient Advocacy to join our Patient Advocacy team, shaping enterprise-wide strategy across discovery, development, and commercialization from our Sleepy Hollow, NY campus. In this role, you'll build the operating model that brings the patient voice into executive decision-making, partnering closely with Medical, Commercial, Market Access, Policy, and Clinical Development. This position offers the opportunity to shape how a fast-growing, science-driven organization listens to and acts on patient needs, making a meaningful difference for people living with serious diseases worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Sleepy Hollow, NY</li><li>Work model/flexibility: Hybrid — onsite 4 days per week</li></ul><p><strong>Discover your role:</strong></p><ul><li>Shape Regeneron’s enterprise-wide patient advocacy strategy, connecting the patient voice to discovery, development, and commercialization.</li><li>Build the standards and governance that guide how we engage advocacy and professional organizations.</li><li>Partner with Medical, Commercial, Market Access, Policy, and Clinical Development to set a multi-year advocacy roadmap.</li><li>Drive measurable outcomes — faster diagnosis, stronger trial awareness, broader access, and a better patient experience.</li><li>Move fluidly between big-picture strategy and hands-on execution, leading through influence across teams.</li><li>Turn corporate priorities into focused, therapeutic-area plans with clear decision rights.</li><li>Read external trends and policy shifts early, and recommend the moves that keep patient impact and business goals aligned.</li><li>Report progress through KPIs, dashboards, and board-ready materials that keep senior leaders informed.</li></ul><p><strong><em>This role might be for you if:</em></strong></p><ul><li>You've built enterprise-level programs from the ground up and know how to earn buy-in across an organization.</li><li>You're comfortable being a visible advisor to senior leaders and advocacy partners alike.</li><li>You bring structure to ambiguity, turning broad strategy into clear, repeatable processes.</li><li>You communicate with precision — able to distill complex work into a concise, data-driven story.</li><li>You’ve partnered across Medical, Commercial, Market Access, and Policy functions and understand the compliance considerations that come with advocacy work.</li><li>You put patients first, and let that perspective shape decisions, budgets, and partnerships.</li><li>You're energized by leading through influence rather than direct authority.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree and 12+ years of relevant experience, including 10+ years leading multi-stakeholder patient advocacy programs</li><li>A track record of building enterprise-wide, cross-functional programs with visible business impact</li><li>Strong executive presence and communication skills, with experience preparing board-ready materials</li><li>Experience partnering with Medical, Commercial, Market Access, and Policy teams, with working knowledge of compliance in advocacy</li><li>Preferred: experience in rare disease, oncology, hematology, ophthalmology, immunology, or cardio-metabolic disease</li><li>Preferred: experience operating in complex, matrixed, or global organizations; alliance management experience is a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Precision Medicine Strategy Lead (Clinical Biomarkers)]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47645]]></requisitionid>
    <referencenumber><![CDATA[R47645]]></referencenumber>
    <apijobid><![CDATA[r47645]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47645/principal-scientist-precision-medicine-strategy-lead-clinical-biomarkers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Precision Medicine Strategy Lead (Principal Scientist) to join our Translational Medicine organization, supporting clinical biomarker strategy for multiple clinical-stage assets across our Immunology & Inflammation, Ophthalmology, and Infectious Diseases portfolios. In this role, you will shape biomarker strategies that enable endpoint selection, indication choice, and demonstration of target engagement and mechanism of action, while collaborating with research teams, clinical development, laboratory operations, companion diagnostics, and external academic and alliance partners.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: 4 days per week</li></ul><p><strong>Discover your role:</strong></p><ul><li>Define and champion the strategic vision and scientific rationale for clinical biomarker plans across I&I, Ophthalmology, and/or Infectious Disease programs</li><li>Represent Precision Medicine on clinical development teams, driving biomarker strategy from concept through execution and interpretation</li><li>Partner with clinical and laboratory operations to implement biomarker and exploratory sample collection and analyses</li><li>Ensure clinical biomarker assays are fit-for-purpose, whether developed internally or through external collaborators and CROs</li><li>Present translational project plans, biomarker data, and results to internal and external stakeholders, including senior leadership</li><li>Contribute high-quality Precision Medicine content to clinical protocols, study reports, data reviews, biomarker reports, and manuscripts/publications</li><li>Translate complex immunology and disease biology into clear, testable biomarker hypotheses and decision criteria</li><li>Navigate ambiguity and prioritize across multiple programs in a collaborative, matrixed environment</li></ul><p><strong>This role requires:</strong></p><ul><li>Ph.D. with post-doctoral experience in Immunology or a closely related field highly desirable; 5+ years of relevant experience in pharmaceutical/biotech research and/or translational clinical development</li><li>Exceptional communication skills and strong emotional intelligence, with enthusiasm for presenting to senior leaders</li><li>Collaborative and innovative mindset, energized by working in a matrixed, cross-functional environment</li><li>Understanding of biomarker strategy in clinical development, including assay development, validation, and implementation</li><li>Preferred: track record of high-impact contributions to drug development programs</li><li>Preferred: experience authoring industry documents (protocols, CSRs, biomarker reports)</li><li>Alternative levels will be considered commensurate with experience.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician (Overnights)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46909]]></requisitionid>
    <referencenumber><![CDATA[R46909]]></referencenumber>
    <apijobid><![CDATA[r46909]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46909/hvac-technician-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an HVAC Technician to join our Facilities Maintenance team. In this role, you will be responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Working hours: Saturday-Wednesday 10:00pm-8:30am</li><li>Training hours: Monday-Friday 7:00am-3:30pm</li><li>Location: Rensselaer, NY</li></ul><h3>Discover your role:</h3><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers.</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work.</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC equipment</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Coordinating with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li></ul><br><h3>This role requires:</h3><ul><li>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level:</li><li>HVAC Technician II: AAS with 2+ years or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years or equivalent combination of education and experience</li><li>HVAC Technician IV: AAS with 8+ years or equivalent combination of education</li><li>Solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>EPA certified for refrigeration gases</li><li>Able to become fully gown qualified to work in production areas</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs (Standard Operating Procedures, cGMPs (current Good Manufacturing Processes), GDPs (Good Documentation Practices) and quality standards</li><li>Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement-Direct]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44723]]></requisitionid>
    <referencenumber><![CDATA[R44723]]></referencenumber>
    <apijobid><![CDATA[r44723]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44723/director-global-procurement-direct/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Global Procurement Direct to join our team supporting our External Manufacturing organization, CMO’s, Drug Substance, Drug Product, and Advanced Therapies on an on-site basis. In this role, you will develop and lead holistic category strategies, build and manage a global CMO procurement team, and drive competitive advantage and supplier performance while collaborating with IOPS stakeholders and Direct Procurement Leadership to enable Regeneron's revenue targets and new product pipeline.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Schedule: Mon-Fri 8:00am- 4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the composition, development, and execution of category strategies across CMO External Manufacturing, Drug Substance, and Drug Product</p></li><li><p>Translates category strategies into achievable sourcing projects that deliver value to Regeneron and its patients</p></li><li><p>Partners with Direct Procurement Leadership and IOPS stakeholders to evolve strategies as Regeneron's pipeline grows</p></li><li><p>Builds and manages a global team providing CMO procurement support, developing talent and driving process excellence</p></li><li><p>Collaborates across Global Procurement to manage cross-category suppliers and executes a best-in-class partner management program</p></li><li><p>Implements technology solutions to drive value through efficiency and effectiveness</p></li><li><p>Serves as a role-model leader, creating clarity, vision, transparency, and trust across the organization</p></li><li><p>Influences and partners with senior executives and peer functions to drive strategic change and efficiency across CMO and External Manufacturing categories</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Director Level: Bachelor's degree in a relevant field and 12+ years of progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma</p></li><li><p>In-depth knowledge of CMOs and External Manufacturing, Raw Materials, or Packaging Technologies within pharmaceutical procurement categories</p></li><li><p>Proven success leading global category teams, processes, and suppliers across a breadth of categories</p></li><li><p>Preferred/nice-to-have: Working knowledge of sourcing and contracting tools, ERPs, and eRFx systems (e.g., Oracle, Zycus, Ariba)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Compliance Specialist-Manufacturing]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49278]]></requisitionid>
    <referencenumber><![CDATA[R49278]]></referencenumber>
    <apijobid><![CDATA[r49278]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49278/sr-compliance-specialist-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Sr Compliance Specialist </strong>to join our <strong>Manufacturing </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Coordination and documentation of manufacturing quality events including Deviations, Change Control’s, Corrective and Preventative Actions </p></li><li><p>Working closely with Manufacturing Managers to review and evaluate quality event information </p></li><li><p>Assess event for impact to SISPQ, conduct risk assessments and initiate appropriate corrective actions to prevent reoccurrence</p></li><li><p>Technical write up and coordination of internal reviews of investigational reports</p></li><li><p>​Participate in management meetings to update leadership on current status of quality events</p></li><li><p>Reviews, edits, and revises controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures</p></li><li><p>Tracks and monitors manufacturings open compliance records</p></li><li><p>Participates in regulatory and customer audits</p></li><li><div><div><p>Utilise problem solving methodologies such as fishbone, 5 Whys etc. to establish root cause of deviations</p></div></div></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><div><div><ul><li><p>Demonstrated skills in problem solving in a cross functional setting, with the ability to keep the team aligned to achieve meeting objectives</p></li><li><p>Ability to work to tight timelines and knows when to escalate actions appropriately for resolution in a timely manner</p></li><li><p>Prior technical writing experience within a manufacturing environment preferred</p></li><li><p>Must have the ability to work in a fast paced environment, with the ability to manage multiple events for on-time closure</p></li><li><p>Must be a highly proactive, detail-oriented individual who has the ability to adapt to change quickly</p></li><li><p>Strong written and verbal communication skills are required</p></li></ul></div></div><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or a related discipline</p></li><li><p>Specialist: 2+ years of relevant work experience</p></li><li><p>Sr Specialist: 5+ years of relevant work experience</p></li><li><p>Relevant experience may be considered in lieu of educational requirements</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p></div><div><div></div><div></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Real-World Data and Analytics (HEOR)]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49658]]></requisitionid>
    <referencenumber><![CDATA[R49658]]></referencenumber>
    <apijobid><![CDATA[r49658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49658/manager-real-world-data-and-analytics-heor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Real-World Data and Analytics (RWDnA) to support the generation of real-world evidence (RWE) in oncology through the analysis of real-world data (RWD). Under the guidance of senior team members, you will be programming on internal RWD assets to support RWE generation to address research questions.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Sleepy Hollow, NY</p><p><br><strong>Discover your role:</strong><br>• Support the development of RWE queries, protocols, and SAPs in the oncology therapeutic area.<br>• Perform analyses of RWD using established methodologies and communicate findings to project teams and RWDnA colleagues.<br>• Support the preparation of presentations, publications, and other communication materials that summarize RWE findings.<br>• Provide operational support for interactions with external analytics vendors, including tracking deliverables and coordinating project activities.</p><p><strong>This role requires:</strong><br>• Doctoral degree in a quantitative field applying data science to healthcare data, or a Master's in a related field with 3+ years of relevant hands-on programming experience<br>• Advanced programming skills in SAS and R<br>• Hands-on experience with real-world data sources such as large-scale administrative claims data (e.g., Optum, Medicare, Komodo) and electronic health records<br>• Proficiency in statistical methods including survival analysis, propensity score methods, and generalized linear models<br>• Ability to work collaboratively in cross-functional environments.<br>• Oncology experience would be preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Life Cycle Management Lead - Oncology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49562]]></requisitionid>
    <referencenumber><![CDATA[R49562]]></referencenumber>
    <apijobid><![CDATA[r49562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49562/senior-director-life-cycle-management-lead-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Senior Director, Global Skin Cancer Life Cycle Management (LCM) Lead is a member of the Oncology Business Unit at Regeneron, responsible for leading life cycle management strategy and planning for all in-line oncology assets within the Skin Cancer tumor area. This leader is a highly strategic, business-focused expert who assesses opportunities and threats for brands in a fast-paced, complex market.</p><p>This role reports directly to the Executive Director of Global Skin Cancer Marketing. The LCM Lead will collaborate closely with cross-functional teams and support the overall strategic goals of the portfolio, playing a critical role in Commercial/Clinical cross-functional forums.</p><p>This individual needs to have strong communication and collaboration skills and will be in involved with leading activities across indications. Based on business needs, support of programming and process across total brand indications is required, which includes managing timelines and eliciting content from the Lung franchise for overall deliverable completion. Examples of select content includes summary reports and planning documents that are applicable across brand indications which are evaluated on a case-by-case basis.</p><p><strong>When & where:</strong></p><ul><li>On site in Sleepy Hollow, NY for 4 days a week</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Facilitate development of and evolution of the global life cycle management strategy (e.g., indication sequencing, geographic expansion) for all in-line oncology assets with Skin Cancer indications to maintain competitive advantage.</li><li>Shape asset plans within Skin Cancer indications in coordination with the Executive Director of Global Skin Cancer Marketing, Regulatory, Clinical, Competitive Intelligence (CI), and other cross-functional partners; partner with US and international marketers to inform and align on the LCM plan.</li><li>Maintain up-to-date tumor landscape outlooks for our portfolio and potential competitors in relevant current and future areas, working with Clinical, CI, and Commercial Insights.</li><li>Share current CI with Global, US, and international marketers and country teams; develop global action plans for competitive threats to be implemented at the country level; develop and deliver related content (e.g., action memos on competitor approvals).</li><li>Support the Executive Director of Global Skin Cancer Marketing in developing the Commercial perspective for Skin Cancer assets in decision-making forums (e.g., Commercial/Clinical cross-functional committees) and cross-tumor planning meetings; help prepare for these meetings and support follow-up actions.</li><li>Lead the Marketing team’s efforts to plan cross-functionally for new indication launches from early development through pre-launch readiness, following established internal processes including identifying working groups cross functionally and across global and country/international teams to facilitate plans and decisions</li><li>Inform Medical Affairs and related teams of key data needs and future development plans the organization will support.</li><li>Develop business analyses/cases for Business Development purposes, for assessing indication trials, and for senior management reviews.</li><li>Serve as the key Marketing point of contact for the Business Development team on Skin Cancer strategy.</li><li>Contribute to labeling review team preparations, providing commercial insights to inform labeling decisions.</li><li>Analyze customer insights, monitor brand performance and competitive dynamics, and translate findings into marketing strategy to address customer needs.</li><li>Leverage customer feedback through formal and informal channels (e.g., advisory boards, KOL meetings at congresses, market research, field intelligence) to shape strategy and competitive differentiation.</li><li>Serve as a member of the cross-functional team that develops and delivers the annual US/Global brand plan, including brand strategy, tactical plans, and budget.</li></ul><p><strong>Operational</strong></p><ul><li>Work closely with Legal and Compliance to ensure all activities meet compliance standards.</li><li>Lead launch-readiness efforts, including cross-organizational planning forum preparation; oversee decision-point team inputs across life cycle stages, track performance metrics, and mobilize functional teams to optimize brand impact.</li><li>Coordinate execution of life cycle levers (e.g., label expansion, access challenges, new formulations, delivery devices).</li><li>Engage regularly with Global Oncology Marketing Leadership, International teams, Clinical Development, Regulatory, Medical Affairs, Market Access, and Sales to align life cycle strategies across functions.</li><li>Provide regular updates on LCM strategy to senior leadership.</li><li>Deliver regular updates to tumor landscape outlook documents and the product strategy guide to align country teams with the long-term LCM strategy.</li><li>Collaborate as needed on globally developed promotional materials for country handoff, especially those aligned to landscape or competitive preparation.</li></ul><br><p><strong>Budgeting</strong></p><ul><li>Work cross-functionally to create, manage, and track US and global budgets within Skin Cancer, ensuring adherence to approved budgets and phasing.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; PhD, PharmD, or MBA preferred.</li><li>12+ years of progressive experience in pharmaceutical marketing, brand strategy, and execution. Oncology experience preferred; Skin cancer experience is a plus.</li><li>Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate.</li><li>Strong scientific acumen with deep knowledge of oncology; ability to understand, partner with, and provide commercial input to all functions within the project team.</li><li>Expertise in early- and late-stage life cycle management for pharmaceutical products, including in competitive environments.</li><li>Previous in-line product and/or indication launch experience required.</li><li>Experience with global, US, or country marketing and pre-approval planning of oncology and/or buy-and-bill drugs required.</li><li>Proven track record of market analysis and identifying growth opportunities on a global scale.</li><li>Ability to synthesize inputs from external and internal collaborators such as HCPs, field teams, country marketers, and market access colleagues.</li><li>Effective written and oral communication; experience delivering complex messages to diverse internal and external collaborators with a track record of influential presentations.</li><li>Ability to communicate and act promptly; demonstrated initiative and creativity; and the agility to work effectively in complex, rapidly changing environments.</li><li>Strong project and process management skills, with the ability to manage multiple tasks and effectively prioritize.</li><li>Proven standout colleague with the ability to navigate cross-functionally.</li><li>Strong analytical skills, both quantitative and qualitative.</li><li>Demonstrated track record of commercial success in roles with progressive responsibilities.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product Lead, Delivery & Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47750]]></requisitionid>
    <referencenumber><![CDATA[R47750]]></referencenumber>
    <apijobid><![CDATA[r47750]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47750/product-lead-delivery-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Regeneron Global Development IT (GD IT) BDM/CGM & ES Lead serves as the Product Lead for the Data Lakehouse and Analytics platforms, partnering with Biostatistics Data Management (BDM), Clinical Genetics Medicine and Experimental Sciences (CGM/ES), compliance, and IT stakeholders to deliver compliant, scalable solutions. This role owns requirements analysis, roadmap alignment, backlog prioritization, and product delivery/execution across these platforms. Success in this role requires strong technical and domain expertise in data transfer and aggregation mechanisms from EDC, non-EDC (e.g., labs, biomarkers, and genetic data) and RWE sources as well as proficiency in R and Python for data management and statistical programming, and experience with AWS, Snowflake and Databricks. Experience is Human Sample Data management from Clinical Trial perspective is a huge plus. The role also demands strong Agile product delivery skills, cross-system integration experience, and adherence to global GxP and regulatory standards. </p><p><strong>When & where: </strong></p><p>Based at our Warren, NJ or Armonk, NY locations.</p><p>4 days on-site per week required. This role is not open to fully remote or hybrid work arrangements.</p><p><strong>Discover your role: </strong></p><div><p>Responsibilities include </p></div><div><ul><li><p>Lead GxP implementation of Data Lakehouse (AWS, Snowflake and Databricks), Posit solutions and support exploratory non-GxP use cases </p></li></ul></div><div><ul><li><p>Provide thought leadership and architectural inputs to shape a scalable future proof modern ecosystem </p></li></ul></div><div><ul><li><p>Manage Human Sample Management as a unified product across sites, labs, EDC systems, and internal LIMS, centralizing data to track specimen location, status, and chain of custody while automating reconciliations </p></li></ul></div><div><ul><li><p>Use AI and agents to enable digital transformation, from strategy to delivery, while remaining complaint and secure </p></li></ul></div><div><ul><li><p>Manage product roadmaps and technical enablement </p></li></ul></div><div><ul><li><p>Lead end-to-end requirements analysis, design, and configuration </p></li></ul></div><div><ul><li><p>Manage scrum and kanban dashboards with team and ensure timely status updates to stakeholders </p></li></ul></div><div><ul><li><p>Gather requirements, manage enhancements, coordinate system changes and user testing, and support release and change management. </p></li></ul></div><div><ul><li><p>Operate within a product based Agile delivery model, owning roadmap execution, backlog prioritization, sprint planning, UAT, release management, and continuous improvement using Jira and ServiceNow. </p></li></ul></div><div><ul><li><p>Drive stakeholder communication, change management, and delivery transparency, including status reporting, risk management, release communications, and cost/budget tracking. </p></li></ul></div><div><ul><li><p>Work with team to create monthly/quarterly stakeholder communications, newsletters </p></li></ul></div><div><ul><li><p>Document standards, processes, and best practices; provide training to technical and non‑technical teams. </p></li></ul></div><div><ul><li><p>Participate in governance forums (steering committees, working groups, change reviews) to ensure alignment and cross‑functional collaboration</p></li><li><p> Develop strong business relationships to clarify needs, anticipate requirements, and ensure solutions meet user expectations. </p></li></ul></div><div><ul><li><p>Establish end to end data governance procedures with stakeholders </p></li></ul></div><p><strong>This role requires: </strong></p><div><ul><li><p>BS/ Degree with 10+ years relevant experience. </p></li><li><p>MS or MBA with 6+ years preferred. Specifically in Life Sciences IT, Product Management, or Business/Systems Analysis with a strong focus on Clinical Data Management and Analytics </p></li></ul><div><ul><li><p>Experience with data lakes/lakehouses (Snowflake, Databricks, AWS) supporting Clinical, RWE, and Safety data </p></li></ul></div><div><ul><li><p>Experience building data pipelines for transfer, cleaning, and aggregation from EDC (RAVE), eCOA, and non-EDC sources (lab, biomarker, genetic/omics data), including API and Regeneron Transfer Service (RTS) integrations </p></li></ul></div><div><ul><li><p>Experience with Human Sample Management </p></li></ul></div><div><ul><li><p>Hands-on proficiency in SAS, R, and Python, including R Shiny development/deployment, APIs, SAS Viya/Posit, and AI automation for clinical R&D </p></li></ul></div><div><ul><li><p>Knowledge of CDISC standards (SDTM, ADaM) and Pinnacle 21 </p></li></ul></div><div><ul><li><p>Understanding of Data Management and Safety functions — signal detection, data quality, query management, lab data reconciliation </p></li></ul></div><div><ul><li><p>Knowledge of CRO data transfer specs and data curation across studies/programs/therapeutic areas </p></li></ul></div><div><ul><li><p>Knowledge of computer system validation, 21 CFR Part 11, GxP, CSV documentation (IQ/OQ/PQ), traceability, change control </p></li></ul></div><div><ul><li><p>Understanding of blinded/unblinded datasets, interim analysis, and DB Lock sensitivities </p></li></ul></div><div><ul><li><p>Experience with ML and visual analytics (feature engineering, training, evaluation) via R, Python, SAS, Posit </p></li></ul></div><div><ul><li><p>Expertise with Generative and Agentic AI (RAG, Agents, MCP, Claude, GPT) </p></li></ul></div><div><ul><li><p>Experience with AWS, DevOps, CI/CD workflows </p></li></ul></div><div><ul><li><p>Experience deploying analytical workloads/Shiny apps to cloud, including production troubleshooting </p></li></ul></div><div><ul><li><p>Experience with CRAN, Git/Bitbucket, version control best practices </p></li></ul></div><div><ul><li><p>Proficiency in Agile Product Lead delivery — backlogs, user stories, sprint planning, UAT, roadmap alignment </p></li></ul></div><div><ul><li><p>Strong analytical and communication skills — translating technical/regulatory requirements for stakeholders </p></li></ul></div><div><ul><li><p>Knowledge of pharma R&D/clinical development processes, SDLC/SSDLC frameworks </p></li></ul></div><div><p><strong>Preferred Qualifications</strong> </p></div><div><ul><li><p>Strong data management and clinical analytics background with data governance experience </p></li></ul></div><div><ul><li><p>Proven experience in designing clinical data repositories, data lakes, data lake houses and optimizing it for multiple teams such as Data Management, RWD, Statistical Programming </p></li></ul></div><div><ul><li><p>Experience providing technical leadership on EDC and Non-EDC data integration into data lakes and data lake houses with other internal systems across business functions </p></li></ul></div><div><ul><li><p>Experience working in a highly matrixed organization and multi-disciplinary team </p></li></ul></div><div><ul><li><p>Experience managing stakeholder expectations and ability to prioritize conflicts </p></li></ul></div><div><ul><li><p>Experience with JIRA for backlog and delivery management; exposure to ServiceNow–JIRA integrations </p></li></ul></div><div><ul><li><p>Certification or equivalent experience in product management </p></li></ul></div><div><ul><li><p>Good understanding of Agentic AI and Generative AI tools and capabilities </p></li></ul></div><div><ul><li><p>Background documenting best practices for configuration, data quality, release management, and governance </p></li></ul></div><div><ul><li><p>Veeva, Salesforce, or Product Management certifications </p></li></ul></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Neurology (Mountain West)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46426]]></requisitionid>
    <referencenumber><![CDATA[R46426]]></referencenumber>
    <apijobid><![CDATA[r46426]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46426/associate-director-field-medical-affairs-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs (Medical Science Liaison) to engage in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. As a scientific expert in your territory, you will demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities to shape our medical strategy. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location/Territory: Kansas City, Minnesota, Colorado, Oklahoma<br>• Travel: (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends.<br>Discover your role:<br>• Establishing, fostering, cultivating and maintain peer relationships with KOLs in Neurology<br>• Acting as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding.<br>• Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.<br>• Support evidence generation (company sponsored trials and investigator-initiated studies) research initiatives.<br>• Identify and report medical insights.<br>• Identifies gaps in research and educational needs to inform medical strategy.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.<br>• Performs disease management and therapeutic area education with identified practitioners, payers and researchers.<br>• Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><p><strong>This role requires:</strong><br>• A Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) with a minimum 8 years of experience, including 4+ years working as a Medical Science Liaison in the pharmaceutical industry. <br>• Experience as a Neurology MSL or in Neurology is preferred. <br>• Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs is required. <br>• Established relationships with KOLs in neuromuscular centers is preferred, as is product launch experience. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. </p><p>#msl #medicalscienceliaison<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44717]]></requisitionid>
    <referencenumber><![CDATA[R44717]]></referencenumber>
    <apijobid><![CDATA[r44717]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44717/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>ion</div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Warren, NJ or Cambridge, MA</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables</p></li><li><p>Lead the development and quality control of tables, listings, and graphs in support of analysis requirements</p></li><li><p>Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests</p></li><li><p>Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch</p></li><li><p>Partner with management to determine resource requirements for your therapeutic area or department</p></li><li><p>Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles</p></li><li><p>Provide feedback to management on team members' contributions to support performance evaluations and goal-setting</p></li><li><p>Advise direct reports on procedures for data, records, and information retention</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Enjoy working with minimal supervision and taking ownership of complex deliverables</p></li><li><p>Communicate clearly with cross-functional, multidisciplinary teams</p></li><li><p>Think analytically and stay organized when managing multiple priorities and timelines</p></li><li><p>Take initiative in developing deep expertise within a specialized area</p></li><li><p>Bring a collaborative mindset to hiring, feedback, and team development</p></li><li><p>Adapt easily to shifting priorities, including last-minute requests from senior leadership</p></li><li><p>Approach quality and documentation with rigor in a regulated environment</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)</p></li><li><p>Proven experience leading programming deliverables within a clinical study team</p></li><li><p>Experience providing input on hiring, feedback, and performance evaluation</p></li><li><p>Strong organizational and documentation skills within a regulated environment</p></li></ul><p><strong>Nice to haves:</strong></p><ul><li><p>SAS Certification</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48340]]></requisitionid>
    <referencenumber><![CDATA[R48340]]></referencenumber>
    <apijobid><![CDATA[r48340]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48340/associate-biotech-production-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Within this role you will be working as part of the Manufacturing Team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors.<br> </p></div><div><p><strong>Where: </strong></p><ul><li><p>Location: Raheen, Limerick</p></li><li><p>Shift: 24/7</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors</p></li><li><p>Monitoring production processes</p></li><li><p>Participating in equipment start-up, commissioning, and validation activities</p></li><li><p>Assisting with troubleshooting in case of equipment failure</p></li><li><p>Performing manufacturing level maintenance on equipment</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Reviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standards</p></li><li><p>Maintaining housekeeping in designated area and adhering to the clean standards of the facility</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You possess excellent verbal and written communication skills</p></li><li><p>You enjoy problem solving</p></li><li><p>You demonstrate a can-do attitude</p></li><li><p>You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook</p></li><li><p>You demonstrate an ability to work within a successful team</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>To be considered for this opportunity you should have a BS/BA in Life Sciences or a related field. Relevant experience may be substituted in lieu of the educational requirement</p></li><li><p>Our site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyle</p></li></ul><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#LI-Onsite #JOBSIEST #REGNIELSM #IRELIM</strong></p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€16.42 - €25.59]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, RNA Therapeutics]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48808]]></requisitionid>
    <referencenumber><![CDATA[R48808]]></referencenumber>
    <apijobid><![CDATA[r48808]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48808/senior-associate-scientist-rna-therapeutics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist/Senior Associate Scientist to join our Nucleic Acid Therapeutics group, supporting drug discovery and technology development in the field of oligonucleotide therapeutics such as siRNAs and antisense oligonucleotides. In this role, you will develop assays and execute high-throughput screenings of hundreds to thousands of candidate molecules, while collaborating with your team to advance oligonucleotide therapeutic programs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop assays to enable high-throughput oligonucleotide library screenings</li><li>Execute high-throughput screening of hundreds to thousands of candidate molecules</li><li>Perform cell culture optimization, bDNA, RT-qPCR, cell line generation, and transfection optimization</li><li>Design probes and conduct compatibility tests, along with western blot analysis</li><li>Work with automated or semi-automated processes, including liquid handlers and instruments such as KingFisher and QuantStudio</li><li>Independently execute and refine techniques and technologies with general guidance</li><li>Multi-task and shift priorities based on communicated department needs</li><li>Thrive in a fast-paced environment, staying detail-oriented, organized, and eager to learn new techniques</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree required; Master's degree preferred</li><li>2+ years of industrial experience in a relevant field highly appreciated</li><li>Ability to independently execute and refine techniques with general guidance, multi-tasking across shifting priorities</li><li>Strong organizational and communication skills, with the ability to work well in a team</li><li>Preferred: experience with automated/semi-automated liquid handlers, KingFisher, and QuantStudio</li><li>Preferred: knowledge of oligonucleotide chemistry and RNA biology</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Therapeutic Area Genetics (Oncology)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46218]]></requisitionid>
    <referencenumber><![CDATA[R46218]]></referencenumber>
    <apijobid><![CDATA[r46218]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46218/director-therapeutic-area-genetics-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We are seeking an exceptional senior leader with deep expertise in cancer genetics and genomics to join our team at the Regeneron Genetics Center. This Director-level role carries full accountability for the strategy and execution of cancer genetic product development — from aligning the vision with senior leadership and translating it into an actionable operational plan, through overseeing product development and setting the strategy for commercialization. The ideal candidate will bring a demonstrated track record of independence and impact, and will serve as the driving force for bringing cancer risk genomics into clinical and commercial reality.</p><div><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><ul><li><p>Develop and deliver on cancer genetics testing opportunities, including germline testing partnerships, serving as the senior leader accountable for clinical cancer test development.</p></li><li><p>Define and own the end-to-end strategy for germline genetic cancer risk product development, translating organizational vision — aligned with senior leadership — into a clear, actionable operational roadmap with measurable milestones.</p></li><li><p>Develop and execute a comprehensive somatic genetics strategy for Regeneron’s oncology portfolio, identifying new opportunities for somatic profiling studies across tumor types and leveraging existing cancer genomics databases.</p></li><li><p>Lead and execute large-scale somatic cancer sequencing analyses, including whole-exome and whole-genome sequencing of tumor samples, RNA-seq, and integrative multi-OMICS studies to identify driver mutations, therapeutic vulnerabilities, and mechanisms of resistance.</p></li><li><p>Design and contribute to cancer molecular profiling and clinical correlation analyses that integrate germline and somatic mutational profiles with multi-modal transcriptomic, epigenetic, and proteomic data to support target discovery, indication selection, and patient stratification strategies.</p></li><li><p> Oversee all phases of product development for cancer risk genomics programs, ensuring scientific rigor, cross-functional alignment, and on-time delivery against strategic objectives.</p></li><li><p>Develop and execute the commercialization strategy for RGC cancer products, identifying market opportunities, go-to-market pathways, and partnerships that maximize clinical and commercial impact.</p></li><li><p>Collaborate with and lead a multidisciplinary genetics team consisting of human genetics scientists, bioinformaticians, and statistical geneticists to design, execute, and interpret genetics studies related to cancer risk, somatic evolution, mechanisms, and therapeutic outcomes.</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>MD or MD/PhD with a strong background in quantitative biology applied to cancer genetics and genomics, and a proven ability to design and lead large-scale human cancer genomic programs delivering medically- and commercially-relevant outcomes.</p></li><li><p>12 years of research experience in cancer genetics, genomics, or oncology product development is required, with a commensurate level of independence, seniority, and demonstrated responsibility for program strategy and execution.</p></li><li><p>Demonstrated ability to independently own and drive strategic programs in cancer risk genomics or oncology product development from conception through commercialization.</p></li><li><p>Bring innovative thinking and hands-on leadership to large-scale somatic cancer sequencing studies and integrative genomic analyses.</p></li><li><p>Have deep expertise in analyzing tumor sequencing data, including variant calling, mutational signature analysis, clonal evolution, copy number alterations, and structural variant detection.</p></li><li><p>Have experience in developing or contributing to germline diagnostic tests for cancer predisposition, risk assessment, or clinical decision-making.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Preclinical & Translational Pharmacokinetics/Pharmacodynamics]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49723]]></requisitionid>
    <referencenumber><![CDATA[R49723]]></referencenumber>
    <apijobid><![CDATA[r49723]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49723/associate-director-preclinical-translational-pharmacokineticspharmacodynamics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Associate Director role involves supporting Pharmacokinetics (PK) and Pharmacokinetics/Pharmacodynamics (PK/PD) requirements for early-stage drug discovery and IND projects. Responsibilities include providing input and oversight for preclinical in vivo studies, coordinating with and influencing scientific teams conducting these studies, managing nonclinical Pharmacokinetics studies, analyzing and presenting PK/PD data to project teams and senior management, and preparing summary reports for regulatory submissions</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: 4 days per week onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Serving as a subject matter expert on Preclinical PK/PD within Discovery-stage project teams and guiding the design of preclinical PK/pharmacology studies.</p></li><li><p>Collaborating with various internal groups such as Therapeutic Proteins, Therapeutic Function Areas, Assay Development, Precision Medicine, Preclinical Operations, and PPK/PD management to develop and execute PK strategies for projects.</p></li><li><p>Effectively communicating project team queries, expectations, and timelines to management.</p></li><li><p>Conducting and reporting PK/PD analyses based on data from preclinical studies.</p></li><li><p>Working closely with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams within the Drug Safety and Pharmacometrics department to deliver data and regulatory documents supporting project progression.</p></li><li><p>Maintaining current knowledge of scientific literature, regulatory guidance, and best practices related to PK/PD.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry with more than 8 to 10 years of relevant experience in biotech or pharma.</p></li><li><p>Deep theoretical and applied understanding of PK and PD to interpret the pharmacology and biology of therapeutic proteins. Experience with other modalities such as siRNA, CRISPR-based therapeutics, and cell therapies is highly beneficial.</p></li><li><p>Proven ability to plan, coordinate, lead PK and/or PK/PD studies, and analyze related data.</p></li><li><p>Familiarity with PK/PD (e.g., WinNonLin), data visualization and AI software and experience writing scientific reports and regulatory summaries.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Precision Medicine (Clinical Diagnostics)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49933]]></requisitionid>
    <referencenumber><![CDATA[R49933]]></referencenumber>
    <apijobid><![CDATA[r49933]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49933/associate-director-precision-medicine-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution. This role owns CDx programs from early biomarker feasibility through clinical validation, regulatory submission, and launch — translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions. You'll work at the interface of biomarker science, clinical development, regulatory, and external In Vitro Diagnostic (IVD) partners to ensure diagnostics keep pace with therapeutic milestones. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Dublin, Ireland (multiple locations are being considered for this role.)</p></li><li><p>Work model/flexibility: 3 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles (TPPs), defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays). </p></li><li><p>Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics.</p></li><li><p>Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints. </p></li><li><p>Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. </p></li><li><p>Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. </p></li><li><p>Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment. </p></li><li><p>Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). </p></li><li><p>Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. </p></li><li><p>Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. </p></li><li><p>8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. </p></li><li><p>Track record translating biomarker science into validated assays supporting drug approvals. </p></li><li><p>Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). </p></li><li><p>Ability to translate complex scientific and clinical data for cross-functional and executive audiences. </p></li><li><p>Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €165,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager-Ophthalmology – Minnesota, Wisconsin]]></title>
    <date><![CDATA[Wed, 22 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49534]]></requisitionid>
    <referencenumber><![CDATA[R49534]]></referencenumber>
    <apijobid><![CDATA[r49534]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49534/field-reimbursement-manager-ophthalmology-minnesota-wisconsin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Wisconsin]]></city>
    <state><![CDATA[Wisconsin]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Ophthalmology Field team. You will use your expertise and knowledge with all Regeneron customers, both internal and external. In this role, you will support physician offices throughout all facets of the reimbursement cycle and work to ensure the lines of communication remain open for existing and future Regeneron products. We always do what is right and seek to fully understand provider business drivers to help develop compliant approaches to account issues and management.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: <strong>Minnesota, Wisconsin</strong></li></ul><p><strong>Discover your role:</strong> </p><ul><li><p>Develop and execute account plans that build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</p></li><li><p>Proactively educate accounts on support services to ensure patient access to care and work with leadership to monitor and track the impact of support services and its interaction/services offered to providers.</p></li><li><p>Develop collaborative relationships with Regeneron colleagues (ex. Regional Directors and Medical Specialists) to educate physician offices in coverage/coding of Regeneron products and support patient access to care.</p></li><li><p>Guide healthcare professionals in resolving reimbursement issues or barriers in a manner that follows Regeneron policies and processes.</p></li><li><p>Anticipate and adapt to the customer’s needs, as well as market changes and challenges.</p></li><li><p>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</p></li><li><p>Establish positive working relationships with accounts (e.g. MD’s, Administrators & office staff) and effectively manage product concerns.</p></li><li><p>Proactively update customers regarding reimbursement requirements, payer trends, and payer policy changes and utilize basket of company approved access materials to support reimbursement confidence.</p></li></ul><p><strong>This role requires:</strong> </p><ul><li><p>Bachelor's degree from a four-year college or university.</p></li><li><p>5-8 years' pharmaceutical/biotech/device experience, including minimum of 3-5 years healthcare coverage, coding and/or reimbursement experience.</p></li><li><p>Previous experience working with billing and medical claims personnel in various health care settings, including, but not limited to a physician office, hospital, HOPD or ASC.</p></li><li><p>Shown expertise in supporting healthcare provider offices with coding, billing, and submissions in range of payer environments. Well versed with implementing and executing Medicare, Medicaid, and other payer initiatives.</p></li><li><p> We expect you to be familiar with CPT, HCPCS, ICD-10, revenue codes and DRG, coverage.</p></li><li><p>Familiarity with health insurance claim forms including UB-04, CMS-1500, explanation of benefits, and prior authorization forms, and super bills charge tickets to troubleshoot cases where billing, claims submission or documentation errors may occur.</p></li><li><p>Ability to analyze, interpret and understand regulatory and legislative payer and healthcare policies.</p></li><li><p>Candidate must reside within assigned territory and have ability to travel 50%-70% of the time.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Commercial Operations Lead, Associate Director]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49945]]></requisitionid>
    <referencenumber><![CDATA[R49945]]></referencenumber>
    <apijobid><![CDATA[r49945]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49945/commercial-operations-lead-associate-director/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are seeking an Associate Director, Commercial Operations Lead to join our Global Capability Center (GCC) Commercial Operations organization. This role will serve as a strategic partner to U.S., international, and global commercial leadership and will be responsible for establishing and scaling Commercial Operations capabilities across HCP Engagement, Marketing Enablement, and Marketing Project Management. Reporting to the Director, GCC Commercial Lead, this position will drive operational excellence, performance monitoring, stakeholder management, and capability-building initiatives that support global commercial strategies and execution across markets.</p><p><strong>When & Where:</strong></p><p><strong>Hyderabad, India (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Provide strategic and operational leadership to Global Commercial Operations and Global Marketing teams, ensuring alignment between global priorities and local execution.</p></li><li><p>Establish and scale the India-based Commercial Operations organization across multiple functional capability areas.</p></li><li><p>Lead and develop teams responsible for HCP Engagement Operations, Marketing Enablement, and Marketing Project Management.</p></li><li><p>Partner with global stakeholders to optimize omnichannel marketing campaigns and project management processes across products and indications.</p></li><li><p>Serve as the primary point of contact for U.S. and international commercial operations leadership regarding operational execution and customer engagement.</p></li><li><p>Drive content operations and marketing enablement initiatives, including MLR review processes, claims management, and digital asset management.</p></li><li><p>Collaborate with Marketing, IT, and in-market teams to localize and deploy promotional materials aligned with global standards and local needs.</p></li><li><p>Develop dashboards, scorecards, KPI tracking, and reporting tools to provide visibility into operational performance and support data-driven decision-making.</p></li><li><p>Monitor commercial operations performance, identify process improvement opportunities, and implement operational excellence initiatives.</p></li><li><p>Ensure compliance with internal policies, industry regulations, and audit requirements across commercial operations activities.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; MBA, Master's degree, or equivalent advanced degree preferred.</p></li><li><p>Minimum 10 years of pharmaceutical/biotech commercial experience, or 7+ years with an MBA/MS, demonstrating increasing levels of responsibility.</p></li><li><p>Proven experience in Commercial Marketing Operations, HCP Engagement Operations, Program Management, and Project Management.</p></li><li><p>Strong understanding of HCP engagement models, operational performance frameworks, metrics, and scorecards.</p></li><li><p>Experience translating global commercial strategies into localized operational plans and supporting execution across diverse international markets.</p></li><li><p>Hands-on experience with content operations, MLR processes, claims management, and Digital Asset Management (DAM).</p></li><li><p>Demonstrated success working with cross-functional and geographically dispersed teams in a global or regulated environment.</p></li><li><p>Experience driving operational excellence, process improvement, and business transformation initiatives.</p></li><li><p>Experience within Global Capability Centers (GCC) or global delivery models in pharmaceutical, biotech, or other regulated industries is preferred.</p></li><li><p>Strong leadership, stakeholder management, communication, and team development capabilities.</p></li><li><p>Strong analytical, problem-solving, and decision-making skills with a focus on continuous improvement and execution excellence</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49413]]></requisitionid>
    <referencenumber><![CDATA[R49413]]></referencenumber>
    <apijobid><![CDATA[r49413]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49413/manager-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager</strong> to join our <strong>Regulatory Affairs Strategy Oncology</strong> team. The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations. </p><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul></div></div><div><p><strong>Discover your role:</strong></p><ul><li><p>Coordinate the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure </p></li><li><p>Assist in coordination and preparation for Agency meetings and associated briefing document preparation </p></li><li><p>Leads and tracks queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments </p></li><li><p>Provide representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum MD, PhD or PharmD degree along with 2+ years of regulatory experience.</p></li><li><p>We expect to see individuals have worked on filings, helped with developing regulatory related documents and engaged with external partners and authorities. </p></li><li><p>If you bring good understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices. </p></li><li><p>If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred </p></li><li><p>If you have a high attention to detail; ability to coordinate and prioritize assigned projects according to company goals </p></li><li><p>You bring strong interpersonal skills both written and verbally </p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Enterprise Stewardship & Standards]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49962]]></requisitionid>
    <referencenumber><![CDATA[R49962]]></referencenumber>
    <apijobid><![CDATA[r49962]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49962/senior-manager-enterprise-stewardship-standards/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Sr. Manager, Enterprise Stewardship & Standards establishes and maintains the foundational semantic and accountability layer of the enterprise data stewardship function. This role leads the enterprise glossary and canonical definitions for cross-domain planning concepts, documents the business rules governing shared planning data, and clarifies steward and data-owner accountability through RACI alignment. The role facilitates cross-functional working forums to drive consensus on shared definitions and standards, and prepares decision records and escalation packages when domains cannot resolve differences on their own. Reporting to the Director, Data Stewardship, this position operationalizes the standards and definitions pillar of the enterprise stewardship operating model and is the first dedicated team member supporting the newly established stewardship function.</p><br><h3>When & where:</h3><ul><li>Location: TarryTown NY, or Warren NJ</li><li>Travel percentage: 10%</li></ul><br><h3>Discover your role:</h3><ul><li>Develop, publish, and maintain the enterprise glossary and canonical definitions for cross-domain planning concepts (e.g., study, program, breakthrough, resource, and financial terms), ensuring a single consistent definition is used across systems, functions, and reports.</li><li>Bachelor Degree or equivalent experience in a related field with at least 7 or more years of experience in biotechnology, pharmaceutical or health related industry</li><li>Author and maintain business-rule documentation for shared planning data, partnering with domain subject-matter experts to validate rule accuracy, ownership, and version history.</li><li>Define and maintain steward and data-owner role clarity across domains through RACI matrices, ensuring accountability for definitions, quality, and lifecycle management is explicit, current, and communicated.</li><li>Plan and facilitate recurring cross-functional working forums that bring together domain owners, Business Process Owners, and stewardship partners to reach alignment on definitions, standards, and business rules.</li><li>Prepare decision records and escalation packages – summarizing the issue, options considered, and collaborator positions – and route unresolved cross-domain conflicts to the Director, Data Stewardship or relevant governance body for resolution.</li><li>Partner with Data Governance to ensure the glossary, canonical definitions, and business rules align with enterprise-wide data policies, standards, and SOPs.</li><li>Collaborate with system Business Process Owners (e.g., Planisware, Planview) and Program, Portfolio Management, and Project Planning leads to ensure standards and definitions reflect planning-system requirements and terminology.</li><li>Support DADS (Data Analytics & Data Science) by ensuring canonical definitions and business rules are correctly and consistently reflected in enterprise analytics, data products, and AI/ML initiatives.</li><li>Track and report on glossary coverage, standards adoption, and forum outcomes, providing input to the broader stewardship roadmap and operating-model maturity.</li><li>Maintain a system of record for definitions, RACI assignments, decision records, and escalation history to support auditability and knowledge continuity.</li></ul><br><h3>This role requires:</h3><ul><li>Solid understanding of drug development, clinical/program planning, and portfolio management terminology and processes.</li><li>Demonstrated experience developing and governing business glossaries, canonical data definitions, and business-rule documentation, ideally within a data governance or data management framework.</li><li>Skilled in developing RACI matrices and clarifying roles and accountabilities across cross-functional stakeholder groups.</li><li>Strong meeting facilitation skills, with a proven ability to drive alignment among stakeholders with competing priorities and to manage conflict constructively.</li><li>Excellent written communication skills, including the ability to produce clear, concise decision records and escalation packages for senior audiences.</li><li>Familiarity with project planning and analytics tools such as Planisware, Planview, Microsoft Project, and Microsoft Office (Word, Excel, PowerPoint).</li><li>Strong analytical and problem-solving skills, with close attention to detail and consistency across data definitions.</li><li>Ability to work independently and collaboratively in a matrixed organization, partnering with Data Governance, DADS, Business Process Owners, and domain data stewards.</li><li>Experience with data governance / business glossary tools (e.g., Collibra, Alation) is a plus.</li><li>Data management or governance certification (e.g., CDMP) and/or PMI Project Management Professional (PMP) is preferred but not required</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Analytical Scientist (Automation)]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48399]]></requisitionid>
    <referencenumber><![CDATA[R48399]]></referencenumber>
    <apijobid><![CDATA[r48399]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48399/principal-analytical-scientist-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Analytical Scientist to join our Quality Control team in Rensselaer, NY, supporting our IOPS organization on-site. In this role, you will shape the future of QC analytical testing by designing, developing, and scaling automated assay workflows across advanced laboratory platforms, while mentoring scientists and fostering a culture of technical growth and innovation. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><div></div><p><strong>When & where</strong></p><p><strong>Location: </strong>Rensselaer, NY (Tempel Lane)</p><p><strong>Work Shift: </strong>Monday-Friday 1st shift</p><p><strong>Discover your role</strong>:</p><ul><li>Lead the design, implementation, and optimization of automated assay workflows across modern laboratory platforms, applying deep expertise in mass spectrometry, chromatography, bioassay, electrophoresis, and ELISA.</li><li>Mentor and develop junior and mid-level scientists, building team capability in analytical science and laboratory automation.</li><li>Set priorities, coordinate work, and track progress on analytical and automation initiatives against key milestones.</li><li>Independently design and execute studies to evaluate emerging automation technologies and troubleshoot existing systems with limited supervision.</li><li>Lead complex investigations into automated method performance, supporting verification activities and driving continuous improvement.</li><li>Transfer automated workflows to QC and partner functions by developing training materials, transfer plans, and acceptance criteria.</li><li>Engage cross-functional collaborators and equipment vendors to evaluate new technologies and assess their fit for QC applications.</li><li>Prepare clear scientific reports, automation procedures, and SOPs; communicate findings, risks, and mitigation strategies to management and cross-functional teams.</li><li>Bring hands-on experience programming and optimizing automated liquid handling systems (e.g., Hamilton/Venus, Andrew+/OneLab, or Cellario) and scripting in Python, R, or VBA.</li><li>Apply strong troubleshooting skills across both analytical methods and automated instrumentation to resolve complex technical challenges.</li><li>Make sound, independent decisions and proactively recommend experiments or solutions based on deep expertise in analytical science and automation.</li></ul><p><strong>This role requires</strong>:</p><ul><li>8+ years of industry experience in analytical development, laboratory automation, and QC method lifecycle management (or equivalent combination of education and experience).</li><li>Demonstrated hands-on expertise in automated liquid handling platforms and associated software programming.</li><li>Proficiency in scripting languages (Python, R, or VBA) for data analysis, workflow automation, or system integration.</li><li>Deep knowledge of QC analytical techniques including mass spectrometry, chromatography, electrophoresis, bioassay, or ELISA.</li><li>Proven ability to work independently, design scientifically sound studies from broad objectives, and drive projects to completion.</li><li><em>Level will be determined based on qualifications at the time of offer.</em></li></ul><p><strong>Preferred:</strong></p><ul><li>PhD in Chemistry, Biochemistry, Biology, or a related field.</li><li>Previous experience working in a cGMP or cGLP regulated environment.</li><li>Familiarity with Cellario, Venus (Hamilton), or OneLab (Andrew+) automation platforms.</li><li>Experience developing and executing technology transfer plans across QC or partner functions.</li></ul><p><strong>Physical Requirements: </strong>Ability to work in a laboratory environment, including standing for extended periods and handling laboratory equipment.</p><p><strong>Gowning & Environment: </strong>This role operates in a GMP analytical laboratory. Appropriate gowning and PPE are required in designated areas.</p><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 03:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior QA Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49282]]></requisitionid>
    <referencenumber><![CDATA[R49282]]></referencenumber>
    <apijobid><![CDATA[r49282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49282/senior-qa-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior QA Specialist </strong>to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Leading and supporting Quality Assurance activities associated with technology transfer projects, ensuring effective knowledge transfer, risk management, and implementation of quality requirements.</p></li><li><p>Providing Quality Assurance project leadership and oversight for the introduction of new manufacturing technologies, equipment, computerized systems, and digital solutions.</p></li><li><p>Partnering with Manufacturing, Engineering, IT, Validation, Supply Chain, and other cross-functional stakeholders to support projects and initiatives across IOPS.</p></li><li><p>Facilitating project governance, risk assessments, and quality decision-making for technology implementation and digitalization programs.</p></li><li><p>Driving the adoption of data-driven and digital approaches that enhance quality processes, visibility, review efficiency, compliance, and operational performance.</p></li><li><p>Supporting the implementation of systems and technologies including Manufacturing Execution Systems (MES), electronic batch records, automation solutions, data integration platforms, and advanced manufacturing technologies.</p></li><li><p>Finding opportunities for process simplification, automation, and digital innovation while ensuring compliance with applicable regulatory requirements and company procedures.</p></li><li><p>Supporting the development of quality strategies, procedures, training materials, and governance frameworks associated with new technologies and digital initiatives.</p></li><li><p>Monitoring project progress, quality risks, and key performance indicators associated with technology transfer, digitalization, and business transformation programs.</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Excellent project, time, and priority management skills, with the ability to independently manage multiple complex assignments simultaneously, adapt to changing priorities, and drive tasks through to successful completion with minimal supervision.</p></li><li><p>Solid understanding of technology transfer principles and lifecycle management within a GMP-regulated environment.</p></li><li><p>Understanding of computerized system implementation, validation principles, data integrity requirements, and applicable regulations including 21 CFR Part 11, Annex 11, and GxP expectations.</p></li><li><p>Familiarity with digital manufacturing systems and technologies, including MES, electronic batch records, automation platforms, data historians, analytics tools, and system integrations.</p></li><li><p>Knowledge of quality risk management methodologies and their application to new technology implementation and process changes.</p></li><li><p>Ability to work optimally across technical and business functions to deliver complex transformation initiatives.</p></li><li><p>Experience supporting continuous improvement, digital transformation, operational excellence, or innovation programs within a regulated industry.</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>BS/BA in scientific discipline or related field with 5+ years or MS 4+ years of relevant work experience in pharmaceutical or related industry or equivalent combination of education and experience.</p></li><li><p>Specialist: 2 years experience</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 03:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46369]]></requisitionid>
    <referencenumber><![CDATA[R46369]]></referencenumber>
    <apijobid><![CDATA[r46369]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46369/associate-biotech-production-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Biotech Production Specialist to join our Global Manufacturing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: We offer multiple shifts that are 4 working days (10 hours), with potentially 1-2 weekend days</li><li>Other requirements: Occasional flexibility may be requested for on-call schedule/weekend work</li></ul><p><strong>What you'll do:</strong></p><ul><li>Cover all facets of drug production in a clean room including cell culture and purification of monoclonal antibodies</li><li>Complete and review batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</li><li>Perform in-process sampling and analysis of buffer solutions, cell culture, and drug substance</li><li>Operate automated equipment such as bioreactors, chromatography columns, and filtration skids</li><li>Support equipment start-up, troubleshooting, and validation</li><li>Partner with R&D teams to implement new drug manufacturing processes and technologies</li><li>Work in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients</li><li>Operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients</li><li>Use computerized systems for daily performance of tasks</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p><strong>Let's find out if we're a fit:</strong></p><ul><li>HS diploma + 4 years of relevant work experience is required</li><li>Or AS, BS or BA in Life Sciences or related field</li><li>Level will be determined based on experience</li></ul><p><strong>Thrive today. Grow Tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.78 - $46.59]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, In Vivo]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50085]]></requisitionid>
    <referencenumber><![CDATA[R50085]]></referencenumber>
    <apijobid><![CDATA[r50085]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50085/associate-scientist-in-vivo/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist to join our Regeneron Genetic Medicines group, supporting in vivo experiments for groundbreaking pre-clinical gene therapy programs. In this role, you will help translate research discoveries into therapeutic candidates, gaining exposure to multiple technologies from discovery phase through clinical development while collaborating in a fast-paced, team-driven environment.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Support in vivo experiments, including injecting viral vectors and other compounds in mice, blood draws, and necropsies</p></li><li><p>Process various samples for downstream analysis</p></li><li><p>Develop and optimize in vivo techniques and translational assays to assess bio-distribution and efficacy of viral vectors in mice</p></li><li><p>Take meticulous notes and communicate professionally with both junior and senior colleagues</p></li><li><p>Work on multiple projects at once, comfortable with quickly shifting priorities</p></li><li><p>Collaborate closely with others in a fast-paced, team-driven environment</p></li><li><p>Bring enthusiasm for working with animals and translating research into therapeutic candidates</p></li><li><p>Seek opportunities to grow your career in gene therapy across discovery and clinical development</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in a related field</p></li><li><p>1+ years of relevant work experience, including mouse handling and familiarity with rodent injection and blood collection techniques</p></li><li><p>Experience with collection and preparation of multiple rodent tissue types for histological analysis</p></li><li><p>Ability to work on multiple projects at once</p></li><li><p>Preferred: comfort asking questions, taking notes, and summarizing high-level takeaways</p></li><li><p>Preferred: experience developing and optimizing protocols, assays, or SOPs</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Program & Portfolio Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49876]]></requisitionid>
    <referencenumber><![CDATA[R49876]]></referencenumber>
    <apijobid><![CDATA[r49876]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49876/associate-director-program-portfolio-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The <strong>Associate Director,</strong> <strong>Program Budget Delivery Lead</strong> is a content-level leadership role embedded within Program & Portfolio Operations (PPO), created to accelerate the consistent, decision-ready delivery of Program Budgets — one of the most critical Strategic Program Team (SPT) deliverables that translate program vision into an actionable, resourced, and costed plan. Deployed selectively alongside SPTs, this role partners directly with the Development Program Manager (DPM) and Program Finance to co-develop key strategic planning deliverables, bringing the drug-development and financial acumen needed to elevate portfolio-level signal and support confident investment decisions.</p><p>This role builds strong, trusted relationships at all levels of the organization, provides content-level leadership that improves consistency and comparability of SPT deliverables, and facilitates decision-making across Development, Research, Commercial, and Manufacturing. Over time, the role is expected to extend its expertise to future high-judgment SPT deliverables while contributing to longer-term capability building across the organization.</p><br><h3>When & where:</h3><ul><li>Location: Tarrytown NY or Warren, NJ</li><li>Travel percentage: <10%</li></ul><br><h3>Discover your role:</h3><ul><li>Partner directly with DPMs, Program Finance and SPTs to co-develop high-quality, decision-ready Program Budgets, embedding drug-development and financial expertise directly within program teams</li><li>Own the quality and timeliness of Program Budget outputs at the CDU and portfolio level, while the DPM retains overall accountability for Program Budget development</li><li>Accurately forecast resource capacity and costs, and build end-to-end development plans and associated costs from IND through lifecycle management (LCM)</li><li>Enable comparison of programs across the portfolio and support portfolio-level investment and prioritization decisions through consistent, comparable outputs</li><li>Manage timely entry and exit points for initial and subsequent Program Budget updates, working in close, ongoing collaboration with the DPM and Program Finance</li><li>Facilitate decision-making and guide SPTs through the strategic planning process, improving consistency and comparability of deliverables across the organization</li><li>Serve as a near-term force multiplier to expedite implementation of Program Budgets with consistent quality, while contributing to longer-term capability building across Program & Portfolio Operations</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor’s degree and 10+ years industry experience with a minimum of 5+ years in project management experience required. MBA preferred.</li><li>Significant experience in the biotechnology or pharmaceutical industry with a strong understanding of drug development activities from early development through lifecycle management</li><li>Strong financial competence with proven experience building and evaluating program budgets, resource forecasts, and development costs</li><li>Proven strategic planning and portfolio management experience, with the ability to synthesize complex program information into clear, decision-ready outputs</li><li>Proven ability to operate as an embedded content expert and thought partner to program leadership, without formal programmatic authority</li><li>Strong organizational and multitasking abilities, supporting multiple programs and SPTs simultaneously under compressed timelines</li><li>Excellent interpersonal skills with a proven ability to negotiate, influence and work effectively with individuals at all levels of the organization, including senior leadership</li><li>Excellent communication skills (written/verbal), including presenting complex financial and strategic information clearly</li><li>IT proficiency with MS software (including Excel-based financial modeling), project management tools and process mapping tools</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, QA Sterility Assurance]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46191]]></requisitionid>
    <referencenumber><![CDATA[R46191]]></referencenumber>
    <apijobid><![CDATA[r46191]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46191/executive-director-qa-sterility-assurance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director, QA Sterility Assurance who leads the strategy, design, and operational execution of Regeneron's GMP contamination control program across aseptic and low-bioburden biopharmaceutical manufacturing operations. This individual provides technical and operational direction to ensure robust environmental control, sterility assurance, and microbial contamination risk management across the network, driving compliance with global regulatory expectations for sterile and non-sterile product manufacturing. This position guides functional areas in support of compliance and business objectives, ensures the contamination control strategy remains current with evolving industry and regulatory expectations, and serves as the key liaison with operational microbiology and manufacturing subject matter experts across the lines of business.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Design, implement, and continuously improve a holistic Contamination Control Strategy (CCS) grounded in sound microbiological science, aseptic processing principles, and applicable quality, regulatory, and legal requirements.</p></li><li><p>Provide expert vision in environmental monitoring (EM) programs, cleanroom classification, personnel qualification, gowning practices, and aseptic process simulation (media fill) performance across manufacturing sites.</p></li><li><p>Influence root cause investigations and risk assessments for microbial excursions, sterility failures, and environmental monitoring deviations, ensuring timely, science-based corrective and preventive actions.</p></li><li><p>Monitor contamination control program performance using meaningful operational metrics (e.g., EM trends, excursion rates, media fill success rates) and demonstrate a commitment to continuous improvement.</p></li><li><p>Embed quality risk management (QRM) tools—such as FMEA and contamination risk mapping—within microbiology and aseptic operations to proactively identify and mitigate contamination vectors.</p></li><li><p>Maintain current expertise in evolving regulatory expectations (e.g., EU Annex 1, FDA Aseptic Processing Guidance, USP <1116>, PIC/S) and proactively integrate emerging requirements into the contamination control program.</p></li><li><p>Apply quality and risk management tools to make timely, science-based decisions that protect patient safety and product sterility.</p></li><li><p>Partner closely with QA Operations, Manufacturing, Facilities/Engineering, and Microbiology Lab functions to translate contamination control strategy into robust, compliant aseptic practices on the floor.</p></li><li><p>Serve as the senior microbiological and contamination control decision-maker, exercising sound judgment under pressure to ensure product safety and efficacy.</p></li><li><p>Represent Regeneron as the subject matter authority on contamination control and sterility assurance to internal leadership, regulatory agencies, and corporate/external partners.</p></li><li><p>Translate contamination control vision and strategy into executable, resourced action plans across the manufacturing network.</p></li><li><p>Ensure the Contamination Control Strategy is transparent, well-documented, and that the broader organization is engaged and accountable for its execution.</p></li><li><p>Establish high standards for performance management and accountability to achieve microbiological, sterility assurance, and organizational objectives.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Microbiology, Molecular Biology, Biology, Pharmaceutical Sciences, or related scientific discipline (advanced degree preferred), or equivalent combination of education and experience, and the following amount of progressive experience in pharmaceutical/biopharmaceutical microbiology, sterility assurance, or contamination control, including significant leadership experience in aseptic manufacturing environments, for each level:</p><ul><li><p>Senior Director – 15+ years</p></li><li><p>Executive Director – 18+ years</p></li><li><p>Level will be determined based on experience</p></li></ul></li></ul><ul><li><p>Deep operational expertise in aseptic processing and low-bioburden manufacturing, including cleanroom design/classification, HVAC airflow principles, personnel and material flow, gowning qualification, and aseptic technique.</p></li><li><p>Demonstrated hands-on ownership of a Contamination Control Strategy (CCS), including environmental monitoring program design, trending, and risk-based EM site selection.</p></li><li><p>Strong working knowledge of aseptic process simulation (media fill) design, execution, and failure investigation.</p></li><li><p>Expert-level understanding of global regulatory expectations and guidance, including EU Annex 1 (2022 revision), FDA Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing, USP <1116>, PIC/S, and ISO 14644.</p></li><li><p>Proven track record leading root cause investigations, deviation management, and CAPA for microbial contamination events, sterility test failures, and environmental excursions.</p></li><li><p>Demonstrated ability to apply Quality Risk Management tools (FMEA, fishbone, risk mapping) to contamination control and microbiological decision-making.</p></li><li><p>Experience representing microbiological/contamination control positions directly to health authorities during inspections (FDA, EMA, MHRA) with a strong inspection track record.</p></li><li><p>Demonstrated success partnering cross-functionally with Manufacturing, Facilities/Engineering, QA Operations, and Microbiology Labs to translate strategy into floor-level execution.</p></li><li><p>Strong people leadership experience, including building and developing high-performing technical teams and driving accountability across a matrixed organization.</p></li><li><p>Excellent judgment and composure in high-stakes, time-sensitive decision-making affecting product disposition and patient safety.</p></li><li><p>Executive presence and communication skills suited to representing the company with regulators, corporate partners, and senior leadership.</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$203,000.00 - $399,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[GCC HR Head]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50022]]></requisitionid>
    <referencenumber><![CDATA[R50022]]></referencenumber>
    <apijobid><![CDATA[r50022]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50022/gcc-hr-head/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, while redefining our understanding of health.</p><p>Regeneron is expanding its international footprint by establishing a new Global Capability Centre (GCC) in Hyderabad, India, in addition to our existing Bangalore office. We are seeking a Senior Director, HR Business Partner, who will serve as the GCC HR Head and lead HR business partnering activities across India. In this role, you will shape and execute the India HR strategy, advise the GCC Leadership Team, oversee locally based HR colleagues supporting global teams, and partner closely with Global HR Centers of Excellence to deliver effective and efficient HR services. You will help strengthen Regeneron’s high-performance culture, the Regeneron Way, while supporting the continued growth of our India organization and GCC capabilities.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Take overall responsibility for the strategic and operational leadership of Regeneron’s HR function in India, while contributing to global and regional HR priorities.</p></li><li><p>Develop and execute the India HR strategy, creating solutions that attract, develop, engage, and retain talent through a strong employer brand, market-competitive total rewards, and agile HR practices.</p></li><li><p>Partner with business leaders, employees, and HR colleagues on workforce planning, talent acquisition, onboarding, development, inclusion, employee engagement, employee relations, performance management, and change management.</p></li><li><p>Serve as a member of the GCC Leadership Team, advising the GCC Head and helping shape the strategy required for the centre to reach its full potential.</p></li><li><p>Lead the daily administration and continuous improvement of core HR activities, including onboarding, talent development, performance management, employee relations, reward, HR policy, engagement, and employee welfare.</p></li><li><p>Provide leadership, coaching, support, and development to India-based HR colleagues, promoting professional standards, capability building, knowledge sharing, engagement, and retention.</p></li><li><p>Partner with Global HR Centers of Excellence, including Employee Services, HR Operations and Technology, People Analytics and Insights, Talent Management, and Total Rewards, to deliver locally appropriate and globally aligned programs.</p></li><li><p>Oversee the day-to-day management and prioritization of locally based HR COE leaders and teams, support blocking issues, and collaborate with Global COE leaders to maximize team impact.</p></li><li><p>Ensure compliance with applicable employment legislation, regulations, professional standards, company policies, and procedures.</p></li><li><p>Coach and support senior leaders and high-potential colleagues, while enabling managers to address workforce matters and effectively navigate the annual performance cycle.</p></li><li><p>Partner with technology teams to develop and enhance market-appropriate HR systems, including Workday and ServiceNow.</p></li><li><p>Manage the HR budget for the India entity.</p></li><li><p>Partner with Regeneron’s Law Department on statutory and employee-related matters, lead employee relations investigations, and ensure appropriate follow-up actions are completed.</p></li><li><p>Translate business needs into actionable HR priorities, systems, and solutions, while sharing standard processes across the International HR Business Partner team and the extended HR Operations and Solutions Leadership Team.</p></li><li><p>Drive continuous improvement by using data, root-cause analysis, and pragmatic solutions to improve productivity, strengthen leadership capability, and create an effective employee experience.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Human Resources, a scientific discipline, or a related field; an MBA or master’s degree in Organization Development or Human Resources is preferred.</p></li><li><p>Minimum of 15 years of HR experience, including experience in an HR or management role within the Indian pharmaceutical, biopharmaceutical, or biotechnology industry.</p></li><li><p>Experience working in a global organization and establishing and growing a Global Capability Centre.</p></li><li><p>Broad experience across multiple HR teams, such as Total Rewards, HR Operations, Talent Management, Talent Acquisition, and Talent Development.</p></li><li><p>Experience supporting or leading across multiple sites is preferred.</p></li><li><p>Proven expertise in talent acquisition and talent development within a technically driven organization.</p></li><li><p>A proven record of initiative, sound prioritization, and an entrepreneurial approach, with the ability to deliver outcomes effectively.</p></li><li><p>Ability to diagnose sophisticated organizational and people challenges, conduct root-cause analysis, and use data to develop pragmatic solutions.</p></li><li><p>Strong quantitative and qualitative analytical capability, with confidence using Microsoft 365 applications, HRIS platforms, and other people-related systems.</p></li><li><p>Learning agility and the ability to operate effectively in ambiguity, translating sophisticated people and data issues into clear, coherent solutions.</p></li><li><p>Strong negotiation, influencing, and stakeholder-management skills, including the courage to challenge established ways of working and focus on doing the right thing.</p></li><li><p>Significant understanding of HR legal and compliance requirements.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Publications]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49903]]></requisitionid>
    <referencenumber><![CDATA[R49903]]></referencenumber>
    <apijobid><![CDATA[r49903]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49903/associate-director-publications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Publications to lead the development and execution of aligned dissemination plans across clinical, HEOR/RWE, PKPD, and disease state publications, while collaborating with cross-functional teams, alliance partners, and leading medical and scientific experts to ensure our research reaches the community accurately and on time.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Warren, NJ or Sleepy Hollow, NY<br>• Work model/flexibility: On-site, 4 days/week (relocation benefits available if eligible; hybrid or fully remote not offered)</p><p><strong>Discover your role:</strong><br>• Lead the development of scientific, clinical, and health-outcomes publications, ensuring accuracy, readability, and timely delivery<br>• Shape the scientific narrative and lexicon behind our data, translating statistical findings into clear strategic communication<br>• Guide cross-functional and alliance-wide publication teams through collaborative discussion, independent research, and strategic alignment<br>• Oversee budget, forecasting, and resource allocation, tracking expenditures and flagging issues early<br>• Partner across functions to identify gaps and opportunities that continually evolve our publication strategy<br>• Accurate and timely reporting of post-publications metrics, compliant maintenance of records in the Publication Management Tool (e.g., iEnvision), vendor and budget management. <br>• Manage timelines, quality, and efficiency across publication activities<br>• Track and report post-publication metrics, maintaining compliant, well-documented records<br>• Review and submit manuscripts, abstracts, and presentations in partnership with cross-functional colleagues</p><p><strong>This role requires:</strong><br>• Master's degree in science with 8+ years of related experience, or PhD/PharmD/MD with 5+ years of experience in medical affairs, publications, or scientific communications<br>• Strong publication, writing, and editing skills<br>• Working knowledge of Good Publication Practice (GPP 22), ICMJE, OIG, PhRMA code, Sunshine Act, and copyright/permission guidelines<br>• Experience collaborating within multi-disciplinary teams and alliances with drug development partners<br>• Oncology, ophthalmology or hematology experience preferred<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - RGM Chemistry]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49786]]></requisitionid>
    <referencenumber><![CDATA[R49786]]></referencenumber>
    <apijobid><![CDATA[r49786]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49786/senior-associate-scientist-rgm-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron Genetic Medicines, we are driven by a mission to transform the treatment of serious diseases through groundbreaking genetic therapies. Our team is at the forefront of innovation, applying cutting-edge science to improve patient outcomes and redefine the future of medicine.</p><p>We are seeking a highly motivated and detail-oriented Senior Associate Scientist to join the RGM R&D Chemistry team with a focus on oligomer and oligonucleotide synthesis, purification, and analytical characterization. The successful candidate will support the design and execution of solid-phase synthesis workflows, contribute to the preparation of modified RNA-related materials, and generate high-quality analytical data to guide platform research and development. This role offers an opportunity to work at the interface of synthetic chemistry, analytical characterization, and RNA therapeutic innovation while contributing to programs that may meaningfully advance future medicines.</p><p><strong> </strong></p><p><strong>What You'll Do:</strong></p><p>Sr. Associate Scientist focused on oligomer synthesis and characterization:</p><ul><li>Execute solid-phase oligomer and oligonucleotide synthesis using automated synthesis platforms, including preparation of reagents, setup of synthesis cycles, incorporation of standard and chemically modified amidites, and on-bead or post-synthetic modifications as needed.</li><li>Support synthesis of RNA-related constructs of varied lengths, formats, and chemical modification to enable discovery, platform development, and cross-functional program needs.</li><li>Develop, optimize, and troubleshoot synthetic workflows to improve yield, purity, reproducibility, and process efficiency.</li><li>Perform purification of synthesized oligomers using appropriate chromatographic techniques, including size-exclusion, anion-exchange, reverse-phase, and ion-pair reverse-phase methods.</li><li>Characterize purified materials using analytical methods such as LC-MS, HPLC/UPLC, UV-Vis, and other orthogonal techniques to confirm identity, purity, concentration, and product quality.</li><li>Analyze and interpret experimental results, summarize findings clearly, and recommend next steps to support iterative chemistry design and platform advancement.</li><li>Maintain accurate, complete, and timely experimental records in accordance with laboratory standards, safety expectations, and internal documentation practices.</li><li>Support routine operation, maintenance, troubleshooting, and inventory management for key synthesis and analytical instrumentation, reagents, and laboratory supplies.</li><li>Collaborate effectively with chemists, biologists, analytical scientists, and project teams to advance RGM Chemistry objectives and communicate technical progress in team discussions.</li></ul><p><strong>Let's Find Out If We're a Fit:</strong></p><ul><li>B.S. in chemistry, biochemistry, chemical biology, biology, or a related scientific discipline is required; Masters degree is preferred</li><li>Minimum of 5 years with BS / 3 years with MS in relevant undergraduate research, internship, or industry experience required.</li><li>Hands-on experience with solid-phase organic synthesis is preferred, particularly oligonucleotide, peptide, oligomer, or related polymer/biopolymer synthesis workflows.</li><li>Nice to have - familiarity with automated synthesis platforms such as MerMade, OligoSynt, or comparable oligonucleotide/oligomer synthesizers is highly desirable. Experience with purification and analytical characterization methods, including SEC, AEX, RP-HPLC or RPIP-HPLC, and LC-MS.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr QA Validation Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49428]]></requisitionid>
    <referencenumber><![CDATA[R49428]]></referencenumber>
    <apijobid><![CDATA[r49428]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49428/sr-qa-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Senior QA Validation Specialist</strong> to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick</li><li>Some travel may be required.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Supervising the end-to-end qualification process ensuring each piece of equipment fits for the intended use that contribute to 365 inspection readiness program</li><li>Following, fostering and implementing a quality culture and other company manufacturing standards, policies and procedures</li><li>Scheduling, executing, reviewing and approving qualification activities</li><li>Assessing executed change controls and deviations for impact to the qualified state for conformance to regulations, SOPs, specifications, and other applicable acceptance criteria</li><li>Investigating and troubleshooting problems which occur and determining solutions or recommendations for changes and/or improvements</li><li>Reviewing, editing, and approving deviation notifications, deviation investigations and corrective actions, change controls, SOPs, reports and other documentation</li><li>Coordinating with other departments and outside contractors/vendors to complete validation tasks</li><li>Managing and driving projects</li><li>Supervising, providing direction and assigning work to less experienced full-time employees (e.g. validation specialists) and/or contingent workers to meet goals and deadlines</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Ability to work independently or as part of a team</li><li>Strong knowledge and understanding of the equipment used for QC analysis and operations</li><li>Ability to communicate with transparency</li><li>Meets commitments on scope and on time</li><li>You have strong knowledge of Data Integrity</li><li>Ability to prioritize and balance multiple tasks simultaneously</li><li>You have project management experience</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>To be considered for this opportunity you must have a BS/BA in Engineering, Chemistry or Life Science and requires at least 5 – 8+ years’ proven experience within the field preferred; may substitute relevant experience for education.</li><li>Previous experience as a SME in a highly regulated environment (e.g. pharma, biotech, medical devices) in both internal and external regulatory audits</li><li>Strong background in site change controls, risk management and data integrity initiatives/programs</li><li>You have expert knowledge of EU annex 11 and FDA 21 CFR Part 11</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQA #REGNQA</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Specialist (Batch Record & Disposition)]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49841]]></requisitionid>
    <referencenumber><![CDATA[R49841]]></referencenumber>
    <apijobid><![CDATA[r49841]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49841/quality-assurance-specialist-batch-record-disposition/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Quality Assurance (QA) Specialist to join our batch record & disposition team. This role performs and leads activities in support of dispositioning product while ensuring compliance with QA policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li><li>Travel percentage: 10% domestic</li></ul><p><strong>Discover your role:</strong></p><ul><li>Represent QA in support of complex and/or significant deviations, change controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</li><li>Represent the IOPS (Industrial Operations Product Supply) organization on behalf of QA with external partners to communicate IOPS QA policy and procedures; liaise with external partners and provide input on issues occurring at external sites</li><li>Provides consultation or advice in alignment with QA policies</li><li>Performs activities associated with disposition of product (e.g. document review, disposition pack preparation, Certificate of Analysis Review)</li><li>Reviews, edits, or approves Regeneron controlled documents</li><li>Reviews and approves investigations associated with raw materials, product, laboratory, facilities, or materials</li><li>Continually evaluate Regeneron processes and procedures with an eye toward continuous improvement</li><li>May train and/or mentor junior employees, including providing insights and education on processes and procedures, and conveying expectations of QA organization</li></ul><p><strong>This role requires:</strong></p><ul><li>B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Associate QA Specialist: 2+ years of experience</li><li>QA Specialist: 4 + years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist – Automation Core]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47919]]></requisitionid>
    <referencenumber><![CDATA[R47919]]></referencenumber>
    <apijobid><![CDATA[r47919]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47919/associate-scientist-automation-core/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>The Automation Core is a centralized high-throughput core laboratory that provides automation services to support technology centers across Research & pre-clinical Development (R&pD). We are seeking an enthusiastic and hard-working Associate Scientist to join the Operations team of the Automation Core, where the candidate will be responsible for the daily operation and routine maintenance of a variety of automated systems. The ideal candidate will be passionate about laboratory automation technologies and eager to collaborate across diverse scientific and engineering functions to achieve organizational goals.</p><p><br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><br><strong>Location: </strong>Tarrytown, NY United States</p><p><strong>Discover your role:</strong></p><ul><li>Operating and troubleshooting automation methods on standalone and integrated systems, including Hamilton, Opentrons, HighRes, and supporting off-the-shelf laboratory devices (dispensers, plate readers/washers, ODTCs, etc.).</li><li>Collaborating with senior team members to review the reservation calendar and alleviate potential system scheduling conflicts.</li><li>Coordinating sample drop-offs and overall logistics with researchers to ensure lab schedules are maintained.</li><li>Performing vendor recommended instrument maintenance to ensure equipment is in peak operational condition.</li><li>Maintaining overall general laboratory housekeeping responsibilities.</li></ul><p><strong>This role requires:</strong></p><ul><li>Work independently on defined tasks and small projects with guidance and supervision from senior colleagues</li><li>Have excellent organizational and communication skills to escalate issues.</li><li>Possess good problem-solving skills necessary to troubleshoot system problems.</li><li>Enjoy collaborating with cross-functional teams in a dynamic research environment.</li><li>Have a positive attitude to learn new workflows and recommend improvements to existing processes.</li><li>Minimum bachelor's degree in life science or related field.</li><li>0-2 years of industry experience working with automation systems within a laboratory environment.</li><li>Relevant internship experience or a great understanding of molecular biology, flow cytometry, genomic, or cell-based assays are highly beneficial for entry level candidates.</li><li>Experience operating liquid handling instruments (E.g., Hamilton STAR) and knowledge of integrated systems is preferred.<br> </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Digital & Technology, Portfolio & Financial Management]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50013]]></requisitionid>
    <referencenumber><![CDATA[R50013]]></referencenumber>
    <apijobid><![CDATA[r50013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50013/senior-director-digital-technology-portfolio-financial-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together:</strong></p><p>We are seeking a Senior Director, Portfolio & Financial Management to join our Digital & Technology, Commercial and G&A Leadership Team. In this role you will establish the strategy, governance, and operating model for portfolio and financial management while driving investment prioritization, value realization, and organizational effectiveness across the technology portfolio. The role also serves as Chief of Staff to the SVP of Commercial and G&A Digital & Technology, acting as a trusted advisor responsible for leadership planning, communications, and execution of key strategic initiatives. Working closely with senior technology, finance, and business leaders, this individual will influence major investment decisions and help ensure technology investments deliver measurable business outcomes.</p><p><strong>When and Where:</strong></p><p><em>This role can sit on-site in our Sleepy Hollow, NY, Rensselaer, NY, or Warren, NJ offices a minimum of 4 days/week. Regular attendance for meetings in Sleepy Hollow is required.</em></p><p><strong>Discover Your Role:</strong></p><ul><li>Lead enterprise technology portfolio management across Commercial and G&A D&T, overseeing intake, prioritization, planning, and investment sequencing based on business value, risk, and delivery capacity.</li><li>Own IT financial management, including budgeting, forecasting, cost transparency, chargeback/allocation models, and technology investment value realization.</li><li>Lead value realization across the Digital & Technology portfolio by developing business cases, defining success metrics, and tracking, monitoring, and reporting realized business value against investment objectives.</li><li>Establish and govern enterprise portfolio and financial management standards, including intake processes, stage-gate reviews, investment frameworks, and governance forums.</li><li>Direct annual and ongoing technology planning cycles, aligning budgets, resource capacity, and prioritization with enterprise strategy and performance objectives.</li><li>Build and mature Technology Business Management (TBM) capabilities, leveraging cost and performance data to improve executive decision-making and demonstrate technology value.</li><li>Lead and develop a high-performing team while driving improvements in portfolio predictability, forecast accuracy, resource utilization, cost visibility, and executive reporting.</li><li>Serve as Chief of Staff to the SVP, managing leadership operating rhythms, strategic initiatives, executive communications, stakeholder engagement preparation, standardized executive reporting, AI-enabled portfolio management initiatives, and key vendor relationships.</li></ul><p><strong>This Role Requires:</strong></p><ul><li>BS/BA in Information Systems, Finance, Business, or a related field required; MS or MBA preferred.</li><li>15+ years of progressive leadership across technology portfolio management, PMO, or IT financial management, ideally within a complex, matrixed enterprise.</li><li>Experience with Planview software is a plus.</li><li>Strong command of portfolio and financial management disciplines (platform-agnostic, e.g., PPM/SPM, technology business management, and stage-gate governance frameworks).</li><li>Experience designing and facilitating executive governance forums, such as steering committees and investment review boards, and driving decisions among senior stakeholders.</li><li>Experience partnering directly with a senior executive in a chief-of-staff, business-management, or executive-office capacity, including executive communications and board-level preparation, is strongly preferred.</li><li>Comfort operating with a high degree of autonomy and discretion, exercising sound judgment on behalf of senior leadership. Proven ability to influence senior leaders, drive accountability across functional areas, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 16:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Head of Regeneron Cell Medicines]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47871]]></requisitionid>
    <referencenumber><![CDATA[R47871]]></referencenumber>
    <apijobid><![CDATA[r47871]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47871/head-of-regeneron-cell-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Head of Regeneron Cell Medicines</strong></p><p>Location: Cambridge, MA (primary site)</p><p>The Head of Regeneron Cell Medicines (RCM) sets the vision, strategy, and execution for Regeneron’s cell medicines portfolio and technology platform. Scope includes ex vivo and in vivo CAR T programs and enabling technologies for delivery, including chemo-free conditioning. This leader oversees cross-functional initiatives from discovery through early clinical development, builds and mentors high-performing teams, and partners across the enterprise and with external collaborators to deliver transformative cell-based therapies. Based in Cambridge, MA, this role serves as the site’s senior scientific executive and advances the RCM portfolio in alignment with Regeneron’s broader scientific vision.</p><p><strong>In This Role, You Will:</strong></p><p><strong>Strategy and Portfolio Leadership</strong></p><ul><li>Define and drive the long-term scientific vision and portfolio strategy for ex vivo and in vivo cell medicines, aligned to enterprise priorities.</li><li>Prioritize programs and platform investments using data-driven governance, scenario planning, and risk/benefit frameworks.</li><li>Champion innovation in cell engineering, in vivo delivery (e.g., LNPs, viral vectors), and manufacturing to create differentiated therapies.</li><li>Establish and evolve the CAR T strategy, including target selection, tissue/cell targeting, potency enhancement, and combinations with antibody-based approaches.</li></ul><p><strong>Scientific Program Oversight</strong></p><ul><li>Lead matrixed teams to deliver milestones from target validation to IND, Phase I manufacturing, and early clinical readouts.</li><li>Guide technical problem solving across modalities, including CAR T design, delivery optimization, biodistribution/PK, on/off-target assessment, and safety risk mitigation.</li><li>Integrate enabling platforms where justified (e.g., CAR Ts, antibody-based approaches such as CPIs and bispecifics, encoded potency enhancements, ARMoR’ing strategies).</li><li>Drive benign conditioning initiatives that enable chemo-free delivery of cell-based medicines (including T cells and hematopoietic stem cells).</li></ul><p><strong>People Leadership and Organizational Development</strong></p><ul><li>Build, mentor, and retain a diverse, high-performing organization of senior scientific leaders and functional experts.</li><li>Foster a culture of scientific excellence, accountability, collaboration, and inclusion across sites and functions.</li><li>Implement succession planning, talent development, and performance management.</li></ul><p><strong>Cross-Functional and Cross-Site Collaboration</strong></p><ul><li>Partner closely with Research, Preclinical Development, Clinical, Regulatory, Quality, CMC, Manufacturing, BD, and Finance.</li><li>Serve as the senior scientific leader for the Cambridge site; maintain strong operating rhythms with Seattle and Tarrytown leadership.</li><li>Coordinate with vector/delivery, immunology, and translational biomarker teams to accelerate RCM programs to clinical evaluation.</li></ul><p><strong>External Innovation and Partnerships</strong></p><ul><li>Identify and evaluate external opportunities (academia, biotech, consortia, platforms) to accelerate the pipeline and capabilities.</li><li>Negotiate and govern collaborations to clear, value-creating outcomes.</li></ul><p><strong>Operational Excellence and Compliance</strong></p><ul><li>Own budgets, headcount planning, and resource allocation across programs and platform functions.</li><li>Ensure adherence to biosafety, ethical guidelines, and regulatory standards (e.g., IND enabling, GxP interfaces), including nonclinical programs specific to ex vivo and in vivo cell therapy (biodistribution, preclinical safety).</li><li>Drive reproducibility, data integrity, and robust decision records.</li></ul><p><strong>Executive Communication and Governance</strong></p><ul><li>Provide clear, concise updates to executive leadership and governance bodies on strategy, progress, risks, and mitigation plans.</li><li>Represent Regeneron Cell Medicines at internal and external forums, scientific conferences, and with partners.</li></ul><p><strong>What You Need to Succeed:</strong></p><p><strong>Required Qualifications</strong></p><ul><li>Advanced degree (PhD, MD, or MD/PhD) in cell biology, immunology, bioengineering, or related discipline.</li><li>20+ years of biopharmaceutical R&D experience with a substantial focus on cell-based therapies; track record advancing programs from discovery to IND and early clinical.</li><li>Demonstrated leadership of multidisciplinary, multisite teams and senior people leaders in a fast-paced environment.</li><li>Deep expertise across key domains:<ul><li>Cell engineering (e.g., CAR design, viral vectors), potency/identity assays, process and analytical development, and translational biology.</li><li>In vivo gene delivery for in vivo CAR T, including viral and non-viral modalities (e.g., LVV, LNPs), tissue/cell targeting strategies, biodistribution/PK, on/off-target risk assessment, and immunogenicity management.</li><li>CMC considerations for in vivo modalities (vector design, release testing, stability) versus ex vivo products.</li></ul></li><li>Familiarity with regulatory pathways for cell and gene therapies (e.g., FDA/EMA guidance, IND preparation, RMAT considerations), including in vivo gene therapy nonclinical packages (biodistribution, toxicology, shedding).</li><li>Strong portfolio management, resource planning, and financial acumen.</li><li>Exceptional communication, influence, and stakeholder management; effective in executive forums and cross-functional decision making.</li><li>Commitment to building an inclusive culture and developing talent.</li></ul><p><strong>Leadership Competencies</strong></p><ul><li>Strategic vision and critical thinking that drive high-quality decisions.</li><li>Scientific rigor and an innovation mindset, balanced by a patient-centric bias for action.</li><li>Talent development and coaching.</li><li>Cross-functional collaboration and influence beyond direct reporting lines.</li><li>Results orientation and accountability.</li><li>Change leadership and resilience.</li></ul><p><strong>Work Model</strong></p><ul><li>On-site presence 4+ days per week in Cambridge, MA; regular travel to Tarrytown, NY and Seattle, WA.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - RALEIGH , NC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48018]]></requisitionid>
    <referencenumber><![CDATA[R48018]]></referencenumber>
    <apijobid><![CDATA[r48018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48018/medical-account-specialist-ii-neurology-raleigh-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Raleigh]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Raleigh (Metro), NC</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NASHVILLE, TN]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48025]]></requisitionid>
    <referencenumber><![CDATA[R48025]]></referencenumber>
    <apijobid><![CDATA[r48025]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48025/medical-account-specialist-ii-neurology-nashville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Nashville-Davidson6]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Nashville (Metro), TN</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - KANSAS CITY, MO - Mountain West]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48067]]></requisitionid>
    <referencenumber><![CDATA[R48067]]></referencenumber>
    <apijobid><![CDATA[r48067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48067/medical-account-specialist-ii-neurology-kansas-city-mo-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Kansas City]]></city>
    <state><![CDATA[Kansas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Kansas City (Metro), MO</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -JACKSONVILLE South, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48029]]></requisitionid>
    <referencenumber><![CDATA[R48029]]></referencenumber>
    <apijobid><![CDATA[r48029]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48029/medical-account-specialist-ii-neurology-jacksonville-south-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Jacksonville]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Jacksonville South (Metro), FL</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - DENVER, CO]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48070]]></requisitionid>
    <referencenumber><![CDATA[R48070]]></referencenumber>
    <apijobid><![CDATA[r48070]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48070/medical-account-specialist-ii-neurology-denver-co/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Denver]]></city>
    <state><![CDATA[Colorado]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Denver (Metro), Co</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Auditor]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47018]]></requisitionid>
    <referencenumber><![CDATA[R47018]]></referencenumber>
    <apijobid><![CDATA[r47018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47018/senior-it-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior IT Auditor is responsible for contributing towards planning, executing, and reporting on operational IT audits, evaluating risks and controls, including application, infrastructure, cloud, data management, SDLC, change management, and IT operations, in accordance with IIA standards and department methodologies. Perform IT SOX control walkthroughs and testing, along with preparing the related documentation. Assess the effectiveness of cybersecurity controls, including identity and access management, vulnerability management, logging and monitoring, incident response, and security governance. <br> </p><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include the following:</strong> </p><div><ul><li><p>Review controls related to cloud computing (e.g., AWS, Azure), SaaS platforms, data lakes, and analytics environments, including shared responsibility models. </p></li></ul></div><div><ul><li><p>Design and execute data analytics‑driven audit procedures using tools such as Dataiku or equivalent, to identify anomalies, trends, and control gaps. </p></li></ul></div><div><ul><li><p>Apply automation, continuous auditing techniques, and responsible use of AI, where appropriate, to improve audit efficiency, coverage, and insight, including assessing AI‑enabled business processes and controls. </p></li></ul></div><div><ul><li><p>Manage timely completion of audit tasks, including communication of status to the auditee and the Manager/Director. </p></li></ul></div><div><ul><li><p>Identify, document, and communicate control deficiencies, root causes, technology risks, and opportunities for improvement, providing practical, actionable recommendations aligned with business objectives. </p></li></ul></div><div><ul><li><p>Present the results of audit work to Internal Audit Management and auditees, including practical recommendations to address identified risks and/or weaknesses in internal controls as well as opportunities to enhance operational efficiencies. </p></li></ul></div><div><ul><li><p>Prepare clear, concise, and professional audit reports and executive‑level presentations for Internal Audit leadership, management, and key stakeholders. </p></li></ul></div><p><strong>This role might be for you if have experience with :</strong></p><div><ul><li><p>Advanced knowledge of IT infrastructure, applications, cybersecurity, and automated controls </p></li></ul></div><div><ul><li><p>Strong understanding of SOX, COSO, COBIT, NIST, GxP, GDPR, and other relevant regulatory and governance frameworks. </p></li></ul></div><div><ul><li><p>Strong analytical, critical‑thinking, and problem‑solving skills, with the ability to independently assess risk and propose solutions. </p></li></ul></div><div><ul><li><p>Comfortable working and learning independently and as part of a team </p></li></ul></div><div><ul><li><p>Excellent interpersonal, communication and writing skills, strong organizational abilities, and attention to detail are required </p></li></ul></div><div><ul><li><p>Experience with data analytical tools (e.g. Dataiku, Alteryx, etc.) </p></li></ul></div><div><ul><li><p>Understanding of AI concepts, associated risks (e.g., model governance, data quality, access, ethical use), and internal controls relevant to AI‑enabled processes. </p></li></ul></div><p><strong>To be considered for this role</strong>, you must have a Bachelor's degree with a<strong> </strong>minimum of 3 - 4 years of progressive experience in IT audit, information security, or technology risk. CISA, CISM and/or CISSP certifications/license preferred. Experience auditing and evaluating infrastructure, cybersecurity risks/controls and auditing operating systems. Pharmaceutical, life sciences, or other regulated industry experience strongly preferred. Big 4 or public accounting experience preferred but not required. </p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director AI, Data & Solutions]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48990]]></requisitionid>
    <referencenumber><![CDATA[R48990]]></referencenumber>
    <apijobid><![CDATA[r48990]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48990/senior-director-ai-data-solutions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are accelerating the adoption of Artificial Intelligence, advanced analytics, and digital innovation to transform how we discover, develop, manufacture, and deliver medicines. We are seeking a Senior Director, AI, Data & Solutions to provide strategic leadership for our enterprise AI, Data, and Digital Solutions organization. In this role, you will shape and implement the enterprise AI and data strategy, build and lead high-performing multidisciplinary teams, drive the delivery of transformative AI and analytics solutions, and partner with executive team members to create measurable business and scientific value. You will play a critical role in helping Regeneron remain at the forefront of innovation while ensuring responsible, scalable, and secure adoption of AI and data technologies.</p><p><strong>When</strong> <strong>&</strong> <strong>where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></p><ul><li><p>Develop and implement a comprehensive AI, Machine Learning, and Data strategy aligned with enterprise priorities across research, development, manufacturing, commercial, and corporate functions.</p></li><li><p>Serve as an enterprise leader with vision and advocate for AI, analytics, and advanced digital solutions, translating emerging technologies into business and scientific outcomes.</p></li><li><p>Accelerate the adoption of Machine Learning, Generative AI, and advanced computational capabilities that support scientific discovery, clinical development, and operational excellence.</p></li><li><p>Design and implement scalable, cloud-native AI and data platforms that enable self-service analytics, governed data access, and rapid deployment of AI solutions.</p></li><li><p>Partner with executive leadership to shape technology and business strategy while providing trusted guidance on AI and data investments.</p></li><li><p>Lead executive communications, strategic briefings, and governance forums that provide insight into portfolio performance, business impact, and future opportunities.</p></li><li><p>Build, mentor, and inspire a diverse team of AI/ML scientists, data engineers, analytics professionals, and solution architects, fostering a culture of innovation, accountability, and continuous learning.</p></li><li><p>Establish strong operating models, communities of practice, and talent development programs to support long-term organizational growth and capability building.</p></li><li><p>Oversee the end-to-end delivery of AI, Data, and Digital Solutions programs from concept through implementation and value realization.</p></li><li><p>Define and implement delivery standards, engineering procedures, and operating methodologies including Agile, MLOps, and DataOps.</p></li><li><p>Establish KPIs and performance metrics to measure solution adoption, operational performance, and business outcomes.</p></li><li><p>Lead enterprise data governance, architecture, and compliance initiatives to ensure quality, security, scalability, and regulatory compliance across data and AI platforms.</p></li><li><p>Drive innovation and continuous improvement by evaluating emerging technologies, optimizing investment portfolios, and seeing opportunities to create enterprise value through AI and data-driven solutions.</p></li></ul><p><strong>This</strong> <strong>role</strong> <strong>requires:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Data Science, Engineering, Mathematics, or a related technical discipline.</p></li><li><p>Advanced degree or equivalent experience (Master's or PhD) in AI, Data Science, Engineering, or a related field preferred.</p></li><li><p>15+ years of progressive experience in AI, Data Analytics, Digital Engineering, or advanced computational technologies.</p></li><li><p>10+ years of leadership experience managing large-scale teams and senior managers within complex, global organizations.</p></li><li><p>Proven experience developing and accomplishing enterprise AI, Machine Learning, and Data Analytics strategies.</p></li><li><p>Demonstrated success delivering AI and data platforms and solutions from strategy through production deployment and business value realization.</p></li><li><p>Deep expertise in AI/ML technologies including Generative AI, Natural Language Processing, Computer Vision, Agentic Systems, and MLOps platforms.</p></li><li><p>Strong experience with cloud-native data platforms and modern data architecture patterns across AWS, Azure, or Google Cloud environments.</p></li><li><p>Expertise in enterprise data governance, data quality, metadata management, and regulatory compliance requirements.</p></li><li><p>Broad technology acumen spanning data engineering, solution architecture, infrastructure, security, and API-based integrations.</p></li><li><p>Exceptional strategic thinking, executive presence, communication, stakeholder management, and organizational leadership capabilities.</p></li><li><p>Experience in life sciences, biotechnology, pharmaceutical, healthcare, or other highly regulated industries.</p></li><li><p>Experience working with GxP-regulated environments and healthcare data regulations.</p></li><li><p>Relevant certifications such as AWS/Azure/GCP Machine Learning certifications, PMP, SAFe, CDMP, or related credentials.</p></li><li><p>Proven track record of converting emerging technologies into measurable business outcomes and enterprise transformation initiatives.</p></li><li><p>Ability to influence senior collaborators and lead complex digital transformation programs across global organizations.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Global Development Solutions]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48996]]></requisitionid>
    <referencenumber><![CDATA[R48996]]></referencenumber>
    <apijobid><![CDATA[r48996]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48996/senior-director-global-development-solutions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Global Development Solutions to join our Global Development Digital & Technology organization. In this leadership role, you will be responsible for building and scaling Global Development technology capabilities within our Global Capability Center while serving as a strategic partner to business and technology leaders worldwide. You will lead the delivery of innovative technology, data, AI, and digital solutions that support Clinical Operations, Biostatistics & Data Management, Regulatory Affairs, Quality, Medical Affairs, and Drug Safety. This role offers a unique opportunity to shape the future of digital transformation in drug development by combining deep industry expertise, technology leadership, compliance excellence, and organizational growth within a highly collaborative global environment.</p><p><strong>When & Where:</strong></p><p><strong>Hyderabad,</strong> <strong>India</strong> <strong>(Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Lead and scale the Global Development Digital & Technology organization within the India Global Capability Center, fostering a high-performance, inclusive, and innovation-driven culture.</p></li><li><p>Build and expand Global Development technology capabilities through strategic hiring, onboarding, talent development, and organizational design.</p></li><li><p>Partner with Global Development and Technology leadership teams to define and implement business-aligned digital strategies that accelerate drug development objectives.</p></li><li><p>Lead end-to-end technology, architecture, data, and AI solution delivery across Agile and traditional delivery models.</p></li><li><p>Drive operational excellence through delivery governance, performance metrics, delivery predictability, and continuous process improvement.</p></li><li><p>Establish and maintain inspection-ready validation programs aligned with GxP requirements, Computer System Validation standards, and data integrity principles.</p></li><li><p>Ensure compliance with applicable regulatory requirements, including 21 CFR Part 11, EU Annex 11, ICH guidelines, and evolving global regulatory expectations.</p></li><li><p>Drive adoption of AI and Generative AI capabilities by identifying and implementing compliant, value-generating solutions across the drug development lifecycle.</p></li><li><p>Act as a strategic advisor to senior collaborators by translating complex scientific and business challenges into scalable technology solutions.</p></li><li><p>Communicate effectively with executive leadership and cross-functional teams across global regions, driving alignment and informed decision-making.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Information Technology, Engineering, Life Sciences, Business, or a related field; advanced degree preferred.</p></li><li><p>Significant leadership experience within pharmaceutical, biotechnology, healthcare, or other highly regulated industries.</p></li><li><p>Deep knowledge of pharmaceutical and biotechnology drug development functions, including Clinical Operations, Biostatistics & Data Management, Regulatory Affairs, Quality, Medical Affairs, and Drug Safety/Pharmacovigilance.</p></li><li><p>Experience leading large-scale technology organizations and global delivery teams across architecture, engineering, data, and AI rigors.</p></li><li><p>Strong understanding of technology platforms supporting Global Development, including CTMS, EDC, Regulatory Information Management systems, Safety systems, Statistical Computing environments, and Clinical Data Repositories.</p></li><li><p>Strong knowledge of GxP compliance, Computer System Validation (CSV/CSVa), ALCOA+ data integrity principles, and global regulatory requirements.</p></li><li><p>Experience establishing and expanding Global Capability Center (GCC) organizations or similar global operating models.</p></li><li><p>Demonstrated experience evaluating, implementing, and governing AI and Generative AI solutions within regulated environments.</p></li><li><p>Proven ability to influence senior stakeholders and operate effectively within complex global matrix organizations.</p></li><li><p>Strong critical thinking, organizational leadership, problem-solving, change management, and executive communication skills.</p></li><li><p>Advanced degree or equivalent experience such as MS, MBA, PharmD, or equivalent.</p></li><li><p>Experience leading global digital transformation initiatives within Clinical Development or Research organizations.</p></li><li><p>Experience working within highly matrixed global organizations across multiple geographies.</p></li><li><p>Strong understanding of emerging technologies, cloud platforms, advanced analytics, and AI-enabled solutions supporting Drug Development functions.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Fill/Finish Associate (Internal Fill/Finish MFG)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41319]]></requisitionid>
    <referencenumber><![CDATA[R41319]]></referencenumber>
    <apijobid><![CDATA[r41319]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41319/fillfinish-associate-internal-fillfinish-mfg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Fill/Finish Associate. The Fill/Finish Associate performs all duties related to the production and support of drug product manufacturing. Works individually, and as part of a team, to support and perform operations to maintain formulation, filling, assembly, labeling and cartoning/packing equipment for parenteral biological products. Seeks to understand and develops proficiency in processes or procedures of increasing complexity.<br> </p><p>When & where:</p><ul><li>We offer multiple shifts that are 4 working days (10 hours) to support 24/7 production</li><li>Location: Rensselaer, New York, United States</li><li>Occasional flexibility may be requested for on-call schedule/weekend work</li></ul><p>What you'll do:</p><ul><li>Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges within isolators or other cleanroom environments; assemble filled product into syringes and autoinjectors; and run state-of-the-art packaging lines to label and configure product for distribution.</li><li>Monitor production operations using process controls and feedback systems (pneumatics, robotics, manual checks, and PLCs) to ensure throughput, quality, and compliance.</li><li>Perform equipment changeovers, cleaning, handling, and installation of interchangeable parts; maintain clean, safe, and inspection-ready workspaces and equipment.</li><li>Maintain gowning qualification, adhere to aseptic/cleanroom behaviors, and perform environmental monitoring and sampling as required.</li><li>Create, follow, and improve SOPs and operating procedures aligned with cGMP and regulatory expectations; ensure compliance during execution and promptly escalate nonconformities.</li><li>Record and review GMP data with ALCOA principles (accurate, legible, attributable, contemporaneous); reconcile product and controlled materials; and ensure complete training documentation.</li><li>Utilize electronic systems (e.g., MES/eBR, LIMS, training systems, and Microsoft Office) to support manufacturing operations and documentation.</li><li>Travel domestically and internationally as needed to support production or technology transfer activities.</li></ul><p>The environment and physical rhythms of the role:</p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Let's find out if we're a fit:</p><ul><li>HS diploma/ GED</li><li>Or AS, BS or BA in Life Sciences or related field</li><li><em>Level is determined on qualifications relevant to the role. </em></li></ul><p>Thrive today. Grow Tomorrow.</p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$16.20 - $38.56]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Marketing - Oncology]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49101]]></requisitionid>
    <referencenumber><![CDATA[R49101]]></referencenumber>
    <apijobid><![CDATA[r49101]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49101/senior-manager-marketing-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Oncology Marketing, Japan to join our Commercial Oncology team, supporting our Japan business in a hybrid work mode. In this role, you will lead local oncology brand marketing strategy and execution for commercialized indications and future launches while collaborating with cross-functional and cross-regional collaborators, Medical Affairs, and the Sales Team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Japan. Hybrid work model. Travel required 10–20%, including some weekends for conferences and meetings.</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead the local brand planning process, analyzing competitive landscape and promotional opportunities.</li><li>Develop customer-focused, differentiated messages for key target audiences across the oncology portfolio.</li><li>Drive external collaborator engagement plans, including national congresses and HCP meetings.</li><li>Partner with Medical Affairs to create and agree an aligned brand strategy.</li><li>Manage local promotional materials and budget in line with approved spend and compliance standards.</li><li>You collaborate confidently across cross-functional and cross-regional teams to align strategy.</li><li>You take ownership to drive the business within a start-up organization.</li><li>You adapt with a flexible mindset in a complex, rapidly changing environment.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree.</li><li>8–10+ years of biotech or pharmaceutical brand marketing experience.</li><li>Business-level English language skills, written and spoken.</li><li>Working knowledge of local healthcare compliance codes and regulations governing promotional activities.</li><li>Expertise managing advertising agencies and suppliers, and developing annual budgets.</li><li>Excellent planning, prioritization, communication, and presentation skills.</li><li>Oncology sales and marketing experience preferred.</li><li>Product launch experience preferred.</li><li>Science background preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Product Management — Enterprise AI Platforms & Tools]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48868]]></requisitionid>
    <referencenumber><![CDATA[R48868]]></referencenumber>
    <apijobid><![CDATA[r48868]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48868/director-product-management-enterprise-ai-platforms-tools/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron’s newly established Enterprise Data & AI organization is built to drive AI transformation and adoption at scale across every part of the organization. This is a high-visibility, high-velocity position where the work is directly tied to business and scientific impact. </p><p>As the product leader for Regeneron's AI platforms and tools, the successful candidate will have the potential for massive impact and help shape how the enterprise builds, accesses, and adopts AI capabilities. The Director Product Management – Enterprise AI Platforms & Tools will set AI platform strategy and roadmap for the platforms and tools that put AI into the hands of colleagues across the organization, from internal AI assistants to secure data-connected applications to agentic solutions. They will translate business needs into clear technical requirements, frame decisions with a transparent view into their assumptions and the rigor behind them and proactively use data to inspire the next generation of capabilities.</p><p>The successful candidate will be part of the Enterprise Data & AI (ED&AI) team within the AI Center of Excellence (AICOE), working closely with the Chief AI Officer, the AI Innovation Leader, the Platform Engineering team, Delivery Managers, and BU IT partners. Together with this network, they will leverage Regeneron's rich data and state-of-the-art infrastructure to deliver platforms that are useful, trusted, and adopted at enterprise scale.</p><p><strong>When & where: </strong> </p><p>This position can be based in any of our Tri- State area campuses: Tarrytown, NY; Sleepy Hollow, NY; Armonk, NY or Warren, NJ.</p><p><strong>Discover your role:</strong></p><ul><li><p>Be responsible for the release strategy and roadmap for Regeneron's AI platforms and tools, aligned to the enterprise digital roadmap.</p></li></ul><ul><li><p>Build business cases to develop, acquire, or invest in new AI/ML capabilities, datasets, platforms, and tools.</p></li></ul><ul><li><p>Prioritize ruthlessly across competing demands, framing recommendations with clear assumptions and analytical rigor.</p></li></ul><ul><li><p>Develop deep insight into colleague and end-user pain points and identify the highest-value opportunities to improve their experience.</p></li><li><p>Lead the technical product development of large-scale AI platforms, machine learning/AI models, and supporting tooling, partnering with engineering and Business Digital teams to ship high-quality deliverables.</p></li><li><p>Define requirements for core platform capabilities — data access, model serving, search/ranking, automation pipelines, and self-serve tools.</p></li></ul><ul><li><p>Guide the use of cloud technologies (AWS, Azure, GCP) for building and deploying automated ML and analytics pipelines.</p></li></ul><ul><li><p>Setting the evaluation framework and criteria, pilot, and deploy new technologies as appropriate, building toward an industry-leading internal AI ecosystem.</p></li></ul><ul><li><p>Drive product adoption: measure usage, gather feedback, and continuously improve.</p></li></ul><ul><li><p>Partner with GCC engineering teams to translate platform architecture decisions and product requirements into well-scoped, production-ready deliverables; maintain ongoing alignment on roadmap priorities, handoff standards, and delivery quality to ensure continuity between applied AI prototyping and GCC-led build and operate.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor's degree in related field required, Masters, MBA, or advanced degree preferred</p></li></ul><ul><li><p>12+ years of progressive experience in technical product management</p></li></ul><ul><li><p>Strong working knowledge of large language models (LLMs), foundation models, and modern generative AI — including their capabilities, limitations, and evaluation.</p></li></ul><ul><li><p>Familiarity with agentic AI: autonomous and multi-step agents, tool use, planning/orchestration, and human-in-the-loop design.</p></li></ul><ul><li><p>Hands-on understanding of emerging interoperability standards, including the Model Context Protocol (MCP) for connecting models to tools and data, and Agent-to-Agent (A2A) protocols for multi-agent coordination.</p></li></ul><ul><li><p>Experience with retrieval-augmented generation (RAG), vector databases, embeddings, and grounding models in enterprise data.</p></li></ul><ul><li><p>Familiarity with prompt engineering, context engineering, fine-tuning, and model customization techniques.</p></li></ul><ul><li><p>Understanding of AI evaluation and observability — building evals, measuring quality/safety, monitoring drift, and managing model/agent performance in production.</p></li></ul><ul><li><p>Awareness of responsible and secure AI practices: guardrails, access controls, data privacy, and AI governance frameworks.</p></li></ul><ul><li><p>Familiarity with MLOps/LLMOps tooling and orchestration frameworks for building, deploying, and maintaining AI applications and pipelines.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development Quality Lead Japan]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45173]]></requisitionid>
    <referencenumber><![CDATA[R45173]]></referencenumber>
    <apijobid><![CDATA[r45173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45173/senior-manager-global-development-quality-lead-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Global Development Quality Lead – Japan, to join our Global Development Quality & Regulatory Compliance team, supporting our Japan affiliate in a hybrid work model. In this role, you will drive quality and compliance in local operations by providing expert guidance and leadership for the Regeneron quality management system supporting GCP, GVP, Medical and Regulatory Affairs. You will collaborate with cross-functional teams and key stakeholders across local and global functions. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Japan<br>Work model: Hybrid</p><p><strong>Discover your role:</strong></p><ul><li>Lead quality and compliance activities for GCP, GVP, Medical and Regulatory Affairs at the Japan affiliate.</li><li>Build strategic partnerships and drive proactive, risk-based quality initiatives, including audits, with key stakeholders.</li><li>Optimize inspection readiness and support inspection preparation for local affiliate operations.</li><li>Contribute to process improvement initiatives and lead projects aligned with quality objectives.</li><li>Manage issue resolution and escalate serious non-compliances through established processes.</li><li>Provide expert guidance, training, and support on international regulations and Regeneron standards.</li><li>Line manage, coach, and mentor junior team members or serve as process owner, as assigned.</li><li>You exemplify a quality mindset, professional conduct, and continuous learning in all interactions.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree (or equivalent experience) and at least 8 years of relevant healthcare/pharmaceutical industry experience.</li><li>Advanced knowledge and application of GCP and/or GVP guidelines, including managing complex quality and compliance issues.</li><li>Experience in quality/compliance or clinical development roles, with expertise in GCP/GVP.</li><li>Proven ability in training, supervising, line management, and staff development.</li><li>Strong project management, planning, prioritization, and time management skills.</li><li>Advanced digital literacy, including Microsoft Office suite.</li><li>Effective communication and stakeholder engagement skills, with ability to influence senior leaders.</li><li>Demonstrated ability to manage multiple priorities with urgency and attention to detail.</li><li>Understanding of risk-based quality management and process improvement.</li><li>Behavioral strengths including integrity, adaptability, critical thinking, and collaborative problem solving.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior External Manufacturing Specialist]]></title>
    <date><![CDATA[Sun, 12 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49067]]></requisitionid>
    <referencenumber><![CDATA[R49067]]></referencenumber>
    <apijobid><![CDATA[r49067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49067/senior-external-manufacturing-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Senior </strong><strong><strong>E</strong>xternal Manufacturing Specialist </strong>to join our <strong>Drug Product Manufacturing </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick.</li><li>Travel: up to 25% (domestic and international), as required.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Serving as a Regeneron operational contact for contract manufacturing and/or business partner sites concerning day-to-day activities.</li><li>Coordinating external manufacturing activities at contract and/or business partner sites.</li><li>Scheduling of all batches, supplying materials and providing direction on shipment of bulk or finished product.</li><li>Tracking and monitoring of cycle times, providing supporting documentation for manufacturing activities and enlisting support from others who will provide any required associated reports and technical expertise.</li><li>Liaising between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners.</li><li>Leading a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.</li><li>Supporting all investigations which concern external manufacturing and associated shipping operations.</li><li>Ensuring product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers and business partners.</li><li>Performing reviews of pre-production master batch records and executed batch records.</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Knowledge of external manufacturing from formulation through the final package.</li><li>Basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.</li><li>Proficient in Excel, PowerPoint, Visio, Word, etc. in addition to experience working within shared work environments.</li><li>Strong interpersonal, written and oral communication skills.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><strong>Associate Specialist</strong>: Requires BS/BA in scientific discipline.</li><li><strong>Specialist</strong>: Requires BS/BA in scientific discipline and 2 years of related experience in cGMP manufacturing operations (clinical and/or commercial) or equivalent combination of education and experience.</li><li><strong>Senior Specialist</strong>: Requires BS/BA in scientific discipline and 5 years of related experience in cGMP manufacturing operations (clinical and/or commercial) or equivalent combination of education and experience.</li></ul><h3>Thrive today. Grow tomorrow.</h3><h3>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLEM</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Manufacturing Compliance (Fill/Finish)]]></title>
    <date><![CDATA[Wed, 15 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49229]]></requisitionid>
    <referencenumber><![CDATA[R49229]]></referencenumber>
    <apijobid><![CDATA[r49229]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49229/director-manufacturing-compliance-fillfinish/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of Manufacturing Compliance who will be accountable for leading and developing the Fill/Finish Manufacturing compliance organization, with direct oversight of Change Control, Manufacturing Investigations and CAPA management functions. This role serves as the primary compliance interface between Fill/Finish Manufacturing and IOPS-level quality, regulatory, and governance bodies — representing the manufacturing function in all compliance escalations, health authority interactions, and cross-functional governance forums. The Director drives a culture of continuous compliance improvement, monitors team KPIs, and ensures the sustained inspection readiness of fill/finish operations. In a supporting and partnering capacity, this role maintains close collaboration with Fill/Finish Operations leadership to align compliance priorities with production objectives and patient supply commitments. This is a leadership role requiring deep GMP expertise, organizational effectiveness, and the ability to lead multi-tiered compliance teams.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Provides leadership, vision, and management to the Manufacturing Compliance & Services team, with direct oversight of Change Control and Manufacturing Investigations sub-teams.</p></li><li><p>Directly oversees the Fill/Finish Change Control program, ensuring timely, risk-based evaluation of all manufacturing changes across equipment, processes, materials, facilities, and systems.</p></li><li><p>Directly oversees the Manufacturing Investigations and CAPA program, including deviation management, root cause analysis, effectiveness checks, and timely closure of GMP events originating from fill/finish operations.</p></li><li><p>Monitors, manages, and reports team KPIs across all compliance sub-functions; presents performance metrics to site and IOPS leadership on a recurring cadence.</p></li><li><p>Conducts trend analysis across investigations and deviations to identify recurring failure modes and systemic improvement opportunities.</p></li><li><p>Represents Fill/Finish Manufacturing at compliance meetings, governance forums, and health authority interactions; leads escalation response for manufacturing compliance issues.</p></li><li><p>Partners with Fill/Finish Operations leadership in a supporting capacity to provide compliance guidance on process challenges, validation activities, and new technology introductions.</p></li><li><p>Leads annual merit performance reviews, develops long-term staffing plans, and collaborates with Directors on annual budget development.</p></li><li><p>Rapidly communicates compliance risks to department Directors and Senior Leadership; resolves issues to mitigate patient supply disruptions.</p></li><li><p>Works effectively across departments including Quality Assurance, Facilities, Engineering, MSAT, Regulatory Affairs, Quality Control, IT, and Supply Chain.</p></li><li><p>Writes, reviews, and/or approves SOPs, specifications, regulatory filings, and other controlled documents; executes QMS assignments (CAPA, Deviation, Investigation, Change Control).</p></li><li><p>Maintains site inspection readiness and represents the manufacturing compliance function during regulatory and client audits; participates in cGMP audits of all production areas.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in any of the physical or biological sciences, or chemical engineering and 12+ years of industry experience or equivalent combination of education and experience.</p></li><li><p>Demonstrated compliance leadership with experience leading multi-tiered QMS functions (Change Control, Investigations, CAPA) in an aseptic biologics GMP manufacturing environment; multiproduct facility experience preferred.</p></li><li><p>Deep working knowledge of GMP regulations (FDA 21 CFR Parts 210/211, EU GMP Annex 1, ICH Q10) and experience interacting with multiple health authorities (e.g., FDA, EMA, PMDA).</p></li><li><p>Must have a sustained mindset for inspection readiness; proven ability to develop and monitor compliance KPIs and translate data trends into actionable improvement strategies.</p></li><li><p>Proven ability to lead cross-functional and direct-report teams; excellent at collaborating across Quality Assurance, Facilities, Supply Chain, Regulatory Affairs, and Engineering to remove barriers and build alignment.</p></li><li><p>Effective communicator across all organizational levels, from frontline manufacturing teams to IOPS Senior Leadership and health authority representatives.</p></li><li><p>Excellent at developing staff, teams, and future compliance leaders; leads by example with a passion for continuous improvement and critical thinking.</p></li><li><p>Strategic thinker who can solve complex compliance challenges, quickly adapt to emerging situations, and interpret data to drive decisions and promote organizational health.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Commercial Finance]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46275]]></requisitionid>
    <referencenumber><![CDATA[R46275]]></referencenumber>
    <apijobid><![CDATA[r46275]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46275/associate-director-commercial-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director, Sales Forecasting & Analytics </strong><strong>(Sleepy Hollow, NY)</strong></p><p>Regeneron Healthcare Solutions, Inc. seeks an Associate Director, Sales Forecasting & Analytics (Sleepy Hollow, NY) to generate, analyze, track and disseminate commercial revenue forecasts, analyze actual sales performance and provide related insights for Regeneron’s marketed and new Oncology products. Develop and maintain patient-based forecast models applying a mix of epidemiology, secondary data, and primary market research-based sources resulting in detailed patient flow buildout and all relevant variables to produce and analyze revenue forecasts. Convert assumptions to demand sales units, gross and net sales. Understand and analyze actuals, perform revenue variance analysis to isolate and articulate performance drivers. Work closely with Commercial Business Unit leaders, their teams and other internal partners to ensure forecast models, associated scenarios, and outputs reflect all relevant assumptions and information related to products and indications covered. Structure and perform analysis independently and conduct research to uncover insights to help the business drive decisions. Work with business partners to understand trends and drivers behind variances within deadlines. Prepare financial reports and packages with financials, charts and other elements/visuals as needed for senior management. Prepare ad-hoc presentations for meetings with stakeholders. Assist Finance leadership and Senior Management colleagues with understanding sales performance with all underlying components and layers (net, gross, price, volume/demand, market share etc.). Stay abreast of market dynamics and competitive landscape for brand including commercial, regulatory, research and development events for competing products and product candidates. 10% domestic travel required.</p><p>SALARY RANGE: $157,200 - $256,600 per year</p><p><strong>Job Requirements</strong><strong>:</strong></p><p>Requires a Bachelor’s degree in Finance, Economics, Health and Data Science, Pharmaceutical Science or a related field and 8 years of progressive, relevant experience including sales forecasting experience in the biotechnology/pharmaceutical industry. Must have experience with: Developing and maintaining patient based forecasting models using epidemiology data for biotech and pharmaceutical products; Creating professional presentations in Microsoft PowerPoint, including transforming financial data into clear, visually compelling slides and graphics, and using data visualization tools like Power BI or Tableau; Advanced Microsoft Excel modeling skills for building Commercial and long-term forecast models; Manipulating raw data to interpret results and provide analysis and insights, using tools like SQL; Using external pharmaceutical sales-related data sources such as IQVIA, Komodo, and HUB; Forecasting for both pre-launch and in-line products; Supporting products in Oncology or Rare Disease, domestically (US) and abroad (International); Gross-to-Net accounting & reporting; Predictive Modeling to develop and implement statistically driven, trend-based forecasts; Creating short-term forecasts (weekly/monthly) for tactical planning and multi-year long term forecasts for strategic planning; Post launch performance tracking and variance analysis; Building scenario-based forecasts, analytics, and diagnostics to quantify risks and provide risk-management guidance; Working across product lifecycle stages including pipeline, launch, in-line, and LOE; and Incorporating pricing, gross to net and access dynamics in buy-and bill settings. 10% domestic travel required.</p><h3>To apply for this position, visit <a href="https://careers.regeneron.com">https://careers.regeneron.com</a> Reference code: R46275.</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Oncology - Alicante, Murcia and Albacete]]></title>
    <date><![CDATA[Wed, 22 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49473]]></requisitionid>
    <referencenumber><![CDATA[R49473]]></referencenumber>
    <apijobid><![CDATA[r49473]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49473/key-account-manager-oncology-alicante-murcia-and-albacete/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist Oncology Territory Management Spain to join our Commercial Oncology team, supporting our Spain oncology business in a field-based role. In this role, you will deliver sales objectives, strengthen healthcare professional engagement, and execute territory plans that improve customer value while collaborating with sales colleagues and key cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. This is a temporary role as a leave of absence, maximum 12 months.</p><p><strong>When & where:</strong></p><p>Location: Spain (Alicante, Murcia, Albacete territory)</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Achieve sales objectives through effective territory budget and expense management.</p></li><li><p>Build healthcare professional relationships using scientific evidence and a patient-focused approach.</p></li><li><p>Develop and maintain territory business plans aligned with market insights and brand strategy.</p></li><li><p>Use key data sources to shape territory actions and customer engagement priorities.</p></li><li><p>Collaborate with stakeholders to deliver business objectives across the territory.</p></li><li><p>Peer-coach sales specialists and share best practices to support team performance.</p></li><li><p>You bring a strategic mindset and manage time effectively to maximize customer value.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree or similar educational background and a minimum 5 years of pharmaceutical sales experience.</p></li><li><p>Previous oncology, pharmacy market, therapeutic area, and medical indication experience.</p></li><li><p>Established network of relevant healthcare professionals.</p></li><li><p>Strong scientific communication and disease-focused selling capabilities.</p></li><li><p>Ability to work compliantly within regulatory and legal guidelines.</p></li><li><p>Hematology experience would be a plus</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Technology Specialist]]></title>
    <date><![CDATA[Tue, 21 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42107]]></requisitionid>
    <referencenumber><![CDATA[R42107]]></referencenumber>
    <apijobid><![CDATA[r42107]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42107/senior-it-technology-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior IT Technology Specialist to join our IOPS IT team, ensuring high-quality service delivery and driving IT and OT solutions across our industrial sites. In this role, you will serve as a Subject Matter Expert in IT/OT risk management, security, and operational excellence — identifying and mitigating risks, overseeing incident management, and ensuring compliance with regulatory and security standards — while collaborating with cross-functional teams, service providers, and third-party partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and implement strategies to identify, assess, and mitigate risks within IT and OT operations, ensuring alignment with organizational goals, compliance standards, and regulatory requirements; advise management and business owners on critical issues</li><li>Monitor endpoint security posture, respond to incidents, and coordinate remediation efforts; support IT/OT network segmentation initiatives in alignment with industry frameworks such as IEC 62443</li><li>Contribute to Enterprise Cyber Resiliency projects, enhancing the organization's ability to withstand, detect, respond to, and recover from cybersecurity incidents across IT and OT environments</li><li>Provide oversight and guidance for major incidents, ensuring coordination of resolving parties, effective stakeholder communication, and thorough post-incident review</li><li>Partner with service providers and third-party teams to ensure quality of service, highest levels of availability and efficiency, and adherence to agreed SLAs benchmarked against industry standards</li><li>Provide direction and oversight across the full lifecycle of IT/OT solutions from initiation through transition, collaborating with internal and external teams to ensure successful delivery</li><li>Support audits and compliance reviews with detailed documentation and insights into IT/OT risk management practices; monitor emerging risks and recommend proactive measures to safeguard systems</li><li>Train and guide team members on risk management protocols, fostering a culture of risk awareness and continuous improvement across IT operations</li><li>Deep experience with ITIL disciplines and service management in large-scale, diverse environments including incident management and escalation procedures</li><li>Experience with operating systems including Microsoft Windows and Linux, and virtualization platforms such as VMware</li><li>Experience with monitoring and security tools such as Splunk, Claroty, and next-generation OT tools preferred</li><li>Proven problem determination and root cause analysis skills; excellent customer-facing, negotiation, and influencing skills with the ability to work effectively with global teams and third-party service providers</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology or a related field</li><li>Senior: 5 years of experience delivering IT/OT services.</li><li>Principal: 8 years of experience delivering IT/OT services.</li><li>Strong GxP experience and experience in highly regulated environments required.</li><li>May consider equivalent combination of education and experience; level determined based on qualifications ​</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$77,600.00 - $148,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - MANCHESTER, NH]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48913]]></requisitionid>
    <referencenumber><![CDATA[R48913]]></referencenumber>
    <apijobid><![CDATA[r48913]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48913/medical-account-specialist-ii-hematology-manchester-nh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New Hampshire]]></city>
    <state><![CDATA[New Hampshire]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li>Field Based: <strong>Geography: </strong><strong>ME, VT, NH</strong></li></ul><ul><li>Location: <strong>Manchester, NH </strong></li></ul><p>​</p><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - ALABAMA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48922]]></requisitionid>
    <referencenumber><![CDATA[R48922]]></referencenumber>
    <apijobid><![CDATA[r48922]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48922/medical-account-specialist-ii-hematology-alabama/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.<strong> </strong></p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: <strong>Pensacola, Mobile, Montgomery, Huntsville, Decatur </strong></p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - GRAND RAPIDS, MI]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48900]]></requisitionid>
    <referencenumber><![CDATA[R48900]]></referencenumber>
    <apijobid><![CDATA[r48900]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48900/medical-account-specialist-ii-hematology-grand-rapids-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Grand Rapids]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: Grand Rapids, MI</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  INDIANAPOLIS, IN]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48899]]></requisitionid>
    <referencenumber><![CDATA[R48899]]></referencenumber>
    <apijobid><![CDATA[r48899]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48899/medical-account-specialist-ii-hematology-indianapolis-in/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Indianapolis]]></city>
    <state><![CDATA[Indiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Indianapolis, IN</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Study Lead]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49337]]></requisitionid>
    <referencenumber><![CDATA[R49337]]></referencenumber>
    <apijobid><![CDATA[r49337]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49337/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p></div><div><p>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - COLUMBIA, SC]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48924]]></requisitionid>
    <referencenumber><![CDATA[R48924]]></referencenumber>
    <apijobid><![CDATA[r48924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48924/medical-account-specialist-ii-hematology-columbia-sc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Columbia, SC</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Medical Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49809]]></requisitionid>
    <referencenumber><![CDATA[R49809]]></referencenumber>
    <apijobid><![CDATA[r49809]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49809/manager-medical-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager Medical Operations Medical Affairs Japan to join our Medical Affairs team, supporting our Japan organization in a hybrid work model. In this role, you will drive compliant and efficient Medical Affairs operations while collaborating with cross-functional stakeholders and Medical Affairs colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Japan</p><p>Hybrid work model</p><p><strong>Discover your role:</strong></p><ul><li>Drive compliant execution of Japan Medical Affairs priorities across therapeutic areas.</li><li>Maintain audit readiness through document management, tracking, and recordkeeping.</li><li>Support Medical Affairs activities in local systems and GxP processes.</li><li>Localize SOPs, work instructions, checklists, and process guides for Japan.</li><li>Lead vendor onboarding and lifecycle management with key stakeholders.</li><li>Manage contracting, procurement, budgets, purchase orders, invoices, and payments.</li><li>Coordinate meetings, advisory boards, congresses, and training event operations.</li><li>You build practical processes that improve quality, efficiency, and transparency.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in life sciences, business, operations, or a related field, or equivalent experience.</li><li>Approximately 7-9+ years of pharmaceutical or biotechnology industry experience.</li><li>Experience supporting Medical Affairs operations, project coordination, vendor management, compliance, or operational support.</li><li>Knowledge of compliance, transparency reporting, document management, procurement, contracting, and regulatory operations.</li><li>Proficiency with Microsoft Office, Veeva, Vault Medical, PromoMats, procurement, contracting, and financial systems.</li><li>Fluency in Japanese and business-level English.</li><li>Ability to manage multiple priorities, vendors, systems, and stakeholders independently.</li><li>Ability to travel for meetings, congresses, events, and business activities.</li><li>Experience with Medical Affairs events, congress logistics, and process governance preferred.</li><li>Knowledge of iCertis, SAP, or similar procurement, contracting, or financial platforms preferred.</li><li>Experience partnering with finance, procurement, legal, compliance, IT, and global teams preferred.</li><li>Strong communication, organization, attention to detail, teamwork, and continuous improvement mindset.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47444]]></requisitionid>
    <referencenumber><![CDATA[R47444]]></referencenumber>
    <apijobid><![CDATA[r47444]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47444/senior-medical-director-clinical-development-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Ophthalmology Therapeutic Area, supporting clinical development programs from first-in-human through registration-enabling studies. In this role, you will serve as scientific and medical lead for clinical team(s), guiding development strategy and regulatory submissions while collaborating with Internal Medicine leadership, executive leadership, development partners, and global regulatory agencies. This role reports to the Vice President, Ophthalmology Therapeutic Area Lead.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY; Cambridge, MA; or Warren, NJ</p></li><li><p><strong>Travel:</strong> 10% to relevant conferences</p></li></ul><br><p><strong>Discover your role:</strong></p><ul><li><p>Act as medical expert and leader in interactions with external stakeholders, internal stakeholders, and decision boards</p></li><li><p>Develop innovative clinical strategies to shorten development cycles amid an evolving regulatory landscape</p></li><li><p>Design efficient, robust Phase 1, 2, and 3 programs</p></li><li><p>Partner with research and discovery teams to inform the next generation of targets in the field</p></li><li><p>Safeguard patient safety in clinical studies and support signal detection from post-marketing surveillance</p></li><li><p>Ensure the quality of clinical documents, including investigator brochures, protocols, study reports, and regulatory submission materials</p></li><li><p>Draft responses to regulatory agency questions and prepare regulatory submission documents</p></li><li><p>Build consensus and drive sound decision-making across dynamic, matrixed clinical teams</p></li></ul><br><p><strong>This role requires:</strong></p><ul><li><p>MD or equivalent medical degree, with board certification or eligibility in Ophthalmology</p></li><li><p>Minimum of 4 years of industry experience in early or late clinical development (candidates with strong academic backgrounds and less experience may be considered)</p></li><li><p>Experience leading proof-of-concept and/or registrational clinical trials, including protocol design and study execution</p></li><li><p>Solid knowledge of global regulatory requirements (ICH) for pharmaceutical development</p></li></ul><p>#MDJobs, #MDJOBSCD, #GDTherapeuticJobs, #Ophthalmology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology - PHILADELPHIA, PA]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49692]]></requisitionid>
    <referencenumber><![CDATA[R49692]]></referencenumber>
    <apijobid><![CDATA[r49692]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49692/medical-account-specialists-hematology-philadelphia-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: <strong>Philadelphia, PA</strong></li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Precision Medicine]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46445]]></requisitionid>
    <referencenumber><![CDATA[R46445]]></referencenumber>
    <apijobid><![CDATA[r46445]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46445/senior-scientist-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Scientist to join our Precision Medicine Quantitative Biomarker Team, driving Translational Medicine initiatives that accelerate biomarker discovery and shape clinical development strategies across the entire internal medicine portfolio. In this role, you will serve as the Precision Medicine quantitative lead, applying innovative analytical, computational, and translational strategies, while partnering with biostatisticians, bioinformaticians, epidemiologists, mathematicians, clinical/research scientists, and external collaborators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Design and oversee exploratory analyses of multi-modal data (genomic, transcriptomic, proteomic, metabolomic, clinical, and other biomarker endpoints) to generate actionable insights</p></li><li><p>Develop scalable, long-term pipelines, workflows, and automation that enhance biomarker discovery and clinical development efforts enterprise-wide</p></li><li><p>Lead development of scientific software and AI-driven tools for querying, visualizing, analyzing, and interpreting data</p></li><li><p>Coordinate cross-functional projects, partnering with Molecular Profiling, RGC, and Therapeutic Area Scientists to design and interpret analyses of disease biology and therapeutic mechanism of action</p></li><li><p>Ensure robustness and reproducibility of exploratory statistical and bioinformatic analyses performed in-house or by external vendors</p></li><li><p>Prepare and deliver data visualizations, manuscripts, reports, and presentations that communicate key findings to leadership and collaborators</p></li><li><p>Lead matrixed teams, rapidly structuring complex, unfamiliar datasets into clear clinical insights and stakeholder-ready presentations</p></li><li><p>Mentor junior scientists, fostering a culture of collaboration, innovation, and scientific rigor.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D. in molecular biology, bioinformatics, computational biology, or a related discipline, with 0-2 years post-doctoral or industry experience</p></li><li><p>Proven track record of leading biomarker and translational-science initiatives in cardiovascular, metabolic, or internal-medicine indications</p></li><li><p>Proficiency in statistical modeling, machine learning, and multi-omics data integration using R, Python, and relevant bioinformatics frameworks</p></li><li><p>Experience implementing scalable workflows on cloud platforms (AWS, GCP, or Azure)</p></li><li><p>Demonstrated ability to communicate complex scientific concepts to diverse stakeholders and translate insights into clinical-development decisions</p></li><li><p>Preferred: experience with version control and AI coding assistants such as Claude Code</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr Global Procurement- Lab Consumables]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44951]]></requisitionid>
    <referencenumber><![CDATA[R44951]]></referencenumber>
    <apijobid><![CDATA[r44951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44951/sr-mgr-global-procurement-lab-consumables/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager of Global Procurement Lab Consumables role supporting our Research and Pre-Clinical Development. In this role, you will develop and manage sourcing strategies, lead strategic sourcing initiatives, and negotiate supplier agreements while collaborating with Procurement management, cross-functional stakeholders to drive cost savings, efficiency, and category performance.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Schedule: Mon-Fri 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Defines and implements the global Lab Consumables Category strategy to serve global and regional business needs</p></li><li><p>Aligns category priorities with Procurement management and cross-functional stakeholders through strategic sourcing initiatives</p></li><li><p>Manages negotiations, contracting, and supplier relationship management activities for the Lab Consumables category, in consultation with the Law department</p></li><li><p>Drives cost savings, cash flow improvement, and other efficiency gains through category management activities</p></li><li><p>Represents Global Procurement in organizational decisions with critical short- and long-term impact on category performance</p></li><li><p>Leverages market intelligence, benchmarking, and supplier engagement to strengthen Regeneron's knowledge of supply market dynamics</p></li><li><p>Applies data analytics, automation, and visualization tools to generate insights and communicate results to stakeholders and senior leadership</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Sr Manager Level: Bachelor's degree in a relevant field + 8+ years of progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma</p></li><li><p>In-depth knowledge of managing global category processes and suppliers</p></li><li><p>Proven success managing suppliers and category processes across a breadth of categories, driving results through effective sourcing, negotiations, contracting, and supplier relationship management</p></li><li><p>Preferred-Experience with sourcing and contracting tools, ERPs, and eRFx or sourcing platform systems (e.g., Oracle, Zycus, Ariba, LabViva, Zageno, Science Exchange, Scientist.com)</p></li><li><p>Preferred-Experience with data analytics and visualization tools (e.g., Power BI, Tableau, Power Automate)</p></li><li><p>Preferred/nice-to-have: Experience managing and implementing inventory management programs and technologies (e.g., RFID, QR codes, consignment, VMI solutions, single-use materials, biore</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Endocrinology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46850]]></requisitionid>
    <referencenumber><![CDATA[R46850]]></referencenumber>
    <apijobid><![CDATA[r46850]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46850/medical-director-clinical-development-endocrinology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Endocrinology team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY, Washington, D.C., or Cambridge, MA</p></li><li><p>Travel: 10% to relevant conferences</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>You guide the Global Clinical Study Team to deliver high-quality trials on time.</p></li></ul><ul><li><p>You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance</p></li><li><p>You lead clinical study and protocol development and present to internal and external stakeholders.</p></li><li><p>You provide clinical and scientific leadership for data review, study reports, and publications.</p></li><li><p>You work closely with cross-functional partners to advance program goals and key deliverables.</p></li><li><p>You collaborate with discovery teams to help shape future targets and development opportunities in the field.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.</p></li><li><p>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</p></li><li><p>Experience in rare disease drug development strongly preferred</p></li><li><p>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</p></li></ul><p>#MDJobsCD, #MDJobs, #GDTherapeuticJobs, #Obesity</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Solid Tumor Oncology (GYN Oncology)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45090]]></requisitionid>
    <referencenumber><![CDATA[R45090]]></referencenumber>
    <apijobid><![CDATA[r45090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45090/medical-director-clinical-development-solid-tumor-oncology-gyn-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Sciences to join our Oncology team, supporting solid tumor drug development, including studies in ovarian cancer. In this role, you will design clinical study concepts, oversee the medical and scientific supervision of clinical trials, and lead the Clinical Team to deliver high-quality program milestones, while collaborating with Clinical Project Managers, Clinical Trial Managers, and Therapeutic Area Program Managers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY</p></li><li><p><strong>Travel: </strong>10% to relevant conferences</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Define clinical trial-related goals and objectives</p></li><li><p>Conduct literature and database research to inform trial design</p></li><li><p>Collaborate with Clinical Project Managers, Clinical Trial Managers, and the Therapeutic Area Program Manager</p></li><li><p>Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings</p></li><li><p>Lead and supervise the Clinical Team to deliver high-quality program milestones on schedule</p></li><li><p>Build and maintain relationships with key study investigators</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MD or MD/PhD with a minimum of 2 years of relevant research experience in industry or the academic research setting</p></li><li><p>Oncology clinical fellowship training with translational and/or clinical research experience strongly preferred</p></li></ul></div><div><div><div><div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs, #Oncology</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director QA Operations]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49916]]></requisitionid>
    <referencenumber><![CDATA[R49916]]></referencenumber>
    <apijobid><![CDATA[r49916]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49916/director-qa-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Quality Assurance to provide the quality support and oversight for drug substance manufacturing operations at the Regeneron Drug Substance (DS) facility. The position is responsible for the QA DS team overseeing any or all of the following production processes: cell culture, centrifugation, chromatography, ultrafiltration/diafiltration (UFDF), and aseptic dispensing of bulk drug substance. The director will provide the leadership, direction, and the overall Quality oversight of the manufacturing area ensuring they meet current FDA and International Regulatory Body requirements.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Build and execute a business strategy that translates vision and corporate goals into departmental objectives</p></li><li><p>Builds and maintains a high performing team of managers, providing effective alignment and communication with functional groups at the site and at other manufacturing sites, to successfully deliver on all commitments. Sets the course for the future- defines priorities, goals and objectives for quality team</p></li><li><p>Provide direction, set performance standards, evaluate, develop performance and inspire direct reports</p></li><li><p>Ensure quality floor staff are appropriately trained to support plant operations, ensuring risks are identified and resolved. Responsibilities include in-process testing oversight, line clearance checks (as necessary), batch record review, return to service requirements have been met and quality-on-the-shop-floor responsibilities of first response to product quality issues in production</p></li><li><p>Provide career development and training advice. Provide regular feedback to direct reports on company and departmental operations</p></li><li><p>Directs the activities of resources, both internal and outside contractors/vendors, with similar technical or functional responsibilities</p></li><li><p>Lead cross functional teams and manages the deliverables for the assigned projects. Drives projects through completion within timeline, quality and budgetary constraints. Interfaces with senior management to report on project and program milestones and to present project needs</p></li><li><p>Provides escalated response for Quality and Compliance issues on the manufacturing floor and assures that decisions are made at the proper level and with the appropriate insights.</p></li><li><p>May provide review and final QA approval of deviations, and other quality events; protocols/reports; change documentation, SOPs; master batch record approval</p></li><li><p>Ensures product, facility, and equipment holds are placed when batch, equipment or system integrity is questioned</p></li><li><p>Responsible for representing the Company and directly interfacing with auditors during regulatory body inspections</p></li><li><p>Ensures periodic informal audits are completed in production</p></li><li><p>Leads teams for tracking of quality activities, metrics, CAPA tracking, etc. Reports metrics and assesses data trends to work with operating departments to facilitate process improvements</p></li><li><p>Develops or supports procedure and process development for continual improvement of cell culture operations, centrifugation/harvest, chromatography, UFDF, viral clearance, aseptic dispensing, filling batch records, and segregation/hold process</p></li><li><p>Provide leadership and direction to the manufacturing and support area departments to ensure a constant state of inspection readiness</p></li><li><p>Requires the ability to influence others to achieve results and to challenge the status quo</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Life Sciences or related field, or equivalent combination of education and experience, and a minimum of 12 years experience in a Quality Operations, Quality Management or manufacturing role, in a late stage or early stage start-up Drug Substance/biologics company</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Research Program Management]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49731]]></requisitionid>
    <referencenumber><![CDATA[R49731]]></referencenumber>
    <apijobid><![CDATA[r49731]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49731/manager-research-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Program Manager to join our Research Program Management team, supporting our antibody platform development and antibody engineering teams in an onsite capacity. In this role, you will independently lead and facilitate collaboration across scientific, technical, and operational functions to drive complex, cross-functional platform development programs forward with clarity, accountability, and alignment to organizational priorities while collaborating with functional leads, platform scientists, and Research and Development leadership.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model: Onsite</li></ul><h3>Discover your role:</h3><ul><li>Execute programs independently, managing projects and tasks with strong awareness of internal and external interdependencies</li><li>Identify and champion resolution of critical gaps, risks, or issues across assigned programs and projects</li><li>Prioritize projects and programs and allocate team resources to align with organizational strategic objectives</li><li>Facilitate collaboration between functional areas to ensure effective, accurate, and timely scientific, technical, and program-related communication</li><li>Tailor communication to your audience, distilling complex information into the most pertinent key points</li><li>Identify key data and functions needed to drive discussion and decision-making as programs move through discovery and drug development</li><li>Champion process improvement initiatives and lead the development of new processes with minimal guidance</li><li>Analyze and identify the need for new systems or tools, and lead efforts to design and implement them</li></ul><h3>This role requires:</h3><ul><li>BS or MS degree in a related field and typically 10+ years of relevant experience; PhD in a related field and typically 5+ years of relevant experience</li><li>Ability to execute programs independently with minimal guidance and manage cross-functional interdependencies</li><li>Strong communication skills, with the ability to facilitate collaboration and tailor messaging across scientific, technical, and operational audiences</li><li>Demonstrated technical expertise in, and possible ownership of, processes, systems, or tools supporting project and program work</li><li>Experience championing process improvement initiatives and developing new processes or systems</li><li>Increasing knowledge of drug discovery and development, with the ability to apply technical knowledge to new concepts</li><li>Managing multiple projects of moderate complexity and identifying the best approach for new assignments</li><li>Leading and influencing teams of varying complexity toward efficient solutions, and exercising good judgment to make quality decisions that affect project teamwork and timelines</li><li>Understanding scientific processes and their cross-functional dependencies at a high level; bringing a growing depth of drug discovery and development knowledge to your work</li></ul><p>​</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45803]]></requisitionid>
    <referencenumber><![CDATA[R45803]]></referencenumber>
    <apijobid><![CDATA[r45803]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45803/director-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director </strong>to join our <strong>Patient Safety</strong> team.</p><p>The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s)/asset(s) assigned within a given therapeutic area (TA), and is the GPS representative on the cross functional strategic program team (SPT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety strategy. This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management. The GPS Director joins Regeneron’s industry leading scientific organization, and has a direct impact on drug development, operations, and commercialization in all relevant global territories.</p></div><div><div><div><div><div><div><div><div><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)</p></li><li><p>Leads cross-functional Safety Monitoring Team (SMT) activities</p></li><li><p>Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)</p></li><li><p>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</p></li><li><p>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </p></li><li><p>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</p></li><li><p>Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.</p></li><li><p>Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.</p></li><li><p>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</p></li><li><p>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</p></li><li><p>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10+ years of total relevant experience in PV and/or relevant medical field or equivalent of industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content). </p></li><li><p>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</p></li><li><p>Clinical experience and/or industry experience in Oncology is a plus</p></li></ul><p>#MDJOBSPS #GDPSJobs</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Commercial GCC Lead - Director Insights and Analytics]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49944]]></requisitionid>
    <referencenumber><![CDATA[R49944]]></referencenumber>
    <apijobid><![CDATA[r49944]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49944/commercial-gcc-lead-director-insights-and-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, GCC Commercial Lead to join our Global Capability Center (GCC) in Hyderabad. This role is a foundational member of Regeneron's first GCC and will drive the expansion and scaling of commercial capabilities across Insights & Analytics, Commercial Operations, and Market Access. The successful candidate will establish best practices, build high-performing teams, and enable a data-driven, customer-centric commercial model while working closely with U.S.-based commercial leadership.</p><p><strong>When & where:</strong></p><p><strong>Location:</strong> Hyderabad, India (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Lead and scale the India-based GCC commercial organization, driving innovation, best practices, and collaboration across teams.</li><li>Serve as a member of the GCC leadership team and contribute to the overall success of the Global Capability Center.</li><li>Build, develop, and mentor high-performing teams through hiring, capability development, and leadership coaching.</li><li>Oversee leaders responsible for Insights & Analytics, Commercial Operations, and Market Access functions.</li></ul><ul><li>Collaborate with global commercial leadership to define and implement the commercial capability roadmap aligned with enterprise strategy and business priorities.</li><li>Partner with U.S.-based commercial leaders to align priorities, manage stakeholder expectations, and ensure seamless execution across time zones.</li><li>Establish knowledge transfer programs with VP-level commercial leaders to support transition, localization of methodologies, and capability building within the GCC.</li><li>Build strong relationships with senior stakeholders and influence strategic business decisions.</li></ul><ul><li>Drive integration of analytics, insights, and operations to support data-driven decision-making and commercial excellence.</li><li>Establish governance frameworks, operating models, and delivery standards across Commercial GCC teams.</li><li>Oversee delivery of analytics, reporting, campaign execution, and operational support across multiple global markets, including the U.S., EU5, and Japan.</li><li>Ensure compliance with regulatory, legal, and internal quality standards across all commercial activities.</li><li>Lead continuous improvement initiatives to enhance efficiency, scalability, and quality of commercial capabilities.</li></ul><p><strong>This role requires:</strong></p><ul><li>Strong understanding of the end-to-end pharmaceutical commercial ecosystem, including Insights & Analytics, Market Access, Sales Operations, Marketing, and Patient Engagement.</li><li>Deep familiarity with commercial data domains including patient, HCP, claims, prescription, payer, CRM, and market datasets.</li><li>Experience using advanced analytics, customer segmentation, performance analytics, and forecasting to support business decisions.</li><li>Knowledge of data strategy, governance, quality, standardization, and scalable data management frameworks.</li><li>Understanding of digital, CRM, and omnichannel engagement ecosystems, including campaign measurement and customer engagement strategies.</li><li>Experience with business intelligence and visualization tools such as Power BI and Tableau.</li><li>Familiarity with commercial operations processes including campaign execution, incentive compensation, territory alignment, and program delivery.</li><li>Understanding of data integration, architecture concepts, multi-source data environments, ETL processes, and analytics enablement.</li><li>Knowledge of regulatory, compliance, and review processes impacting commercial content and engagement.</li><li>Experience building and scaling global capability models, operating frameworks, and service delivery structures.</li></ul><ul><li>Proven leadership experience managing large, cross-functional teams.</li><li>Strong strategic thinking with the ability to translate business priorities into execution.</li><li>Excellent stakeholder management skills, including experience working with senior leadership teams.</li><li>Strong communication and influencing skills across all organizational levels.</li><li>Ability to thrive in high-growth, evolving environments and lead organizational transformation.</li><li>Strong problem-solving and continuous improvement attitude.</li><li>Comfortable working across global time zones and collaborating with U.S.-based leadership.</li><li>10+ years of experience in pharmaceutical or biotechnology commercial functions, including significant leadership experience across Insights & Analytics, Commercial Operations, Market Access, or related domains.</li><li>Demonstrated success in building and scaling high-performing teams.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I, Purification Development]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49938]]></requisitionid>
    <referencenumber><![CDATA[R49938]]></referencenumber>
    <apijobid><![CDATA[r49938]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49938/process-development-engineer-i-purification-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Process Development Engineer </strong>to join our <strong>PMPD </strong>team. In this role, you will be responsible for the purification of various pre-clinical biological molecules to provide reagents and therapeutics for Regeneron’s research and discovery groups. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours, with flexibility to support before- and after-hours</li><li>Location: On-Site in Tarrytown, NY</li><li>Flexibility & travel: Some travel required. Must be available on-site consistently, including to maintain coverage during staff absences</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Purification of a diverse array of proteins to support many of Regeneron’s research and discovery groups</li><li>Process development for clinical processes</li><li>Development of technology and automation to increase process throughput and efficiency of preclinical manufacturing</li><li>Documentation of experiments, results, and findings in an electronic laboratory notebook; presentation of work at group and department meetings.</li><li>Maintenance of instruments and troubleshooting of instrumental/experimental problems</li><li>Collaboration with peers to complete core deliverables while exhibiting independence in experimental execution and troubleshooting</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>A fast-paced pilot scale laboratory setting where sound science and team work are priorities.</li><li>Contribute to lab equipment maintenance and safety to help create a safe, effective, and efficient working environment.</li><li>Anticipate and recognize potential problems with laboratory supplies / equipment and act to prevent and tackle problems.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><p>The role requires a Bachelors degree in either Chemical Engineering, Biochemical Engineering, or Biochemistry, and 3+ years’ or a MS and 0-3 years of experience in the biotech or pharmaceutical industry. A strong fundamental understanding of various protein purification techniques a plus. Experience with Downstream Development and with equipment like Akta Explorers/Avants/Pilots, chromatography columns, tangential flow filters, depth filters, HPLCs, and UPLCs as well as software such as Empower, Unicorn, JMP, and LIMS is a plus. Job will periodically require short duration physical exertions, including light-medium weight lifting.</p><h3><strong>Thrive today. Grow tomorrow. </strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Instrumentation & Calibration Technician]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48771]]></requisitionid>
    <referencenumber><![CDATA[R48771]]></referencenumber>
    <apijobid><![CDATA[r48771]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48771/instrumentation-calibration-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Calibration Technician</strong> to join our <strong>Facilities Operations </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Shift Requirements: 24/7</li><li>Location: Raheen, Limerick</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Complying with site safety policies and strive to maintain an accident-free environment.</li><li>Executing scheduled, corrective, and post-maintenance calibrations of process and utility instrumentation in accordance with approved procedures and GMP requirements.</li><li>Performing loop checks, I/O verification, functional testing, commissioning activities, and return-to-service assessments.</li><li>Troubleshooting and resolving instrumentation and low-voltage control system issues to support reliable and uninterrupted manufacturing operations.</li><li>Calibrating, verifying, and maintaining a wide range of instrumentation including temperature, pressure, flow, level, and analytical devices.</li><li>Configuring and verifying smart instrumentation using approved calibration and communication tools.</li><li>Ensuring calibration and maintenance activities are documented in accordance with cGMP, GDP, and Data Integrity requirements.</li><li>Maintaining accurate calibration records, equipment histories, certificates, and work orders within site CMMS and calibration management systems.</li><li>Supporting investigations, deviations, impact assessments, root cause analysis, CAPA activities, and out-of-tolerance events as required.</li><li>Coordinating activities with Manufacturing, Engineering, Validation, Quality, and Facilities personnel to safely and efficiently complete assigned work.</li><li>Maintaining calibration standards, tools, and test equipment in a qualified state with appropriate certification and traceability.</li><li>Supporting facility start-ups, shutdowns, capital projects, and continuous improvement initiatives including Lean and 5S programs.</li><li>Adhering to and remaining current in assigned IOPS plant and departmental SOPs and required training programs.</li><li>Continuously developing technical knowledge and contributing to the success of a high-performing team supporting the manufacturing of life-changing medicines.</li><li>Occasionally performing other processes, utility, facility, and project-related activities outside normal calibration responsibilities in support of site objectives.</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>A time-served Instrumentation/Electrical qualification or relevant third-level qualification in Instrumentation, Electrical/Electronic Engineering, Mechatronics, or a related discipline.</li><li>Relevant experience in calibration, instrumentation, and control systems, preferably within a GMP-regulated environment.</li><li>Experience calibrating temperature, pressure, flow, level, and analytical instrumentation; experience with control valves and weighing systems is an advantage.</li><li>The ability to interpret P&IDs, loop drawings, wiring diagrams, and technical documentation.</li><li>Strong fault-finding and troubleshooting skills across instrumentation and low-voltage control systems.</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>A relevant recognised Trade qualification, third level qualification is preferred; along with 2+ years of experience in a similar position. Will substitute additional relevant experience for educational requirement.</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€14.55 - €37.18]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44853]]></requisitionid>
    <referencenumber><![CDATA[R44853]]></referencenumber>
    <apijobid><![CDATA[r44853]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44853/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables</li><li>Lead the development and quality control of tables, listings, and graphs in support of analysis requirements</li><li>Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests</li><li>Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch</li><li>Partner with management to determine resource requirements for your therapeutic area or department</li><li>Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles</li><li>Provide feedback to management on team members' contributions to support performance evaluations and goal-setting</li><li>Advise direct reports on procedures for data, records, and information retention</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Enjoy working with minimal supervision and taking ownership of complex deliverables</li><li>Communicate clearly with cross-functional, multidisciplinary teams</li><li>Think analytically and stay organized when managing multiple priorities and timelines</li><li>Take initiative in developing deep expertise within a specialized area</li><li>Bring a collaborative mindset to hiring, feedback, and team development</li><li>Adapt easily to shifting priorities, including last-minute requests from senior leadership</li><li>Approach quality and documentation with rigor in a regulated environment</li></ul><p><strong>This role requires:</strong></p><ul><li>Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)</li><li>Proven experience leading programming deliverables within a clinical study team</li><li>Experience providing input on hiring, feedback, and performance evaluation</li><li>Strong organizational and documentation skills within a regulated environment</li></ul><p><strong>Nice to haves:</strong></p><ul><li>SAS Certification</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology (f/m/d)]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49973]]></requisitionid>
    <referencenumber><![CDATA[R49973]]></referencenumber>
    <apijobid><![CDATA[r49973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49973/director-international-commercialization-immunology-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Munich, Germany - multiple locations are being considered for this role</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>125.250,00 € - 208.750,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regulatory Affairs Strategy - Genetics Medicine]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48560]]></requisitionid>
    <referencenumber><![CDATA[R48560]]></referencenumber>
    <apijobid><![CDATA[r48560]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48560/director-regulatory-affairs-strategy-genetics-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Regulatory Affairs Strategy </strong>team.<strong> </strong></p><p>The Director, Regulatory Affairs Strategy will provide leadership on global regulatory activities for assigned products within the Genetic Medicine portfolio. This role is focused on regulatory strategy and filings, with responsibility for providing regulatory leadership across project teams. Consistent with our hands-on culture, the Director will be actively involved in clinical study support and will lead IND/CTA and BLA submission activities.</p><p>The Director will develop and maintain regulatory strategy at the study, indication, and program level, lead interactions with global health authorities, and serve as a key cross-functional partner and subject matter expert. This role also carries people management responsibility, including mentoring and developing regulatory staff.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing interpretation of regulatory authority feedback, policies, and guidelines, and communicating strategic implications to project teams and senior management.</p></li><li><p>Leading the development and maintenance of regulatory strategic plans, either directly in conjunction with project teams or through direct reports. Owning the preparation of major clinical submissions required for regulatory approvals.</p></li><li><p>Working with cross-functional project teams to resolve complex regulatory issues, utilizing deep expertise in global regulations and guidances to strategically plan and communicate requirements.</p></li><li><p>Ensuring the quality and timeliness of regulatory submissions for IND/CTA/BLA; collaborating with other functions and partners in the preparation, review, and completion of submission documents.</p></li><li><p>Leading health authority interactions, including preparation of briefing books and meeting slides, and advising relevant stakeholders on agency feedback.</p></li><li><p>Representing regulatory affairs at senior program team meetings, providing strategic input and direction as a subject matter expert.</p></li><li><p>Planning, prioritizing, and overseeing regulatory activities in close collaboration with leads from other functions to ensure compliance and alignment with project timelines.</p></li><li><p>Mentoring and developing regulatory staff, providing direction and supporting career growth.</p></li><li><p>You bring a strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development processes, and industry standard practices.</p></li><li><p>You have demonstrated success leading regulatory strategy and health authority interactions across global programs, with the ability to influence cross-functional teams and senior leadership.</p></li><li><p>You are comfortable operating in ambiguous, fast-paced environments and can manage multiple programs and priorities simultaneously.</p></li><li><p>You have experience managing or interacting with CROs in the management of ex-US/ex-EU CTAs toward clinical trial activations.</p></li><li><p>You bring strong interpersonal and communication skills, both written and verbal, with the ability to produce persuasive and high-quality regulatory documents.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An MD, Ph.D., Pharm.D., or equivalent advanced degree; a relevant scientific discipline is strongly preferred.</p></li><li><p>A minimum of 10 years of pharmaceutical or biotechnology industry experience, with at least 7 years in regulatory affairs, including direct experience as a regulatory liaison.</p></li><li><p>This role requires onsite presence 4 days per week in Tarrytown, NY or Warren, NJ. Relocation support is available for qualified candidates.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Developer - Research and Development]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48042]]></requisitionid>
    <referencenumber><![CDATA[R48042]]></referencenumber>
    <apijobid><![CDATA[r48042]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48042/senior-developer-research-and-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking an outstanding Senior Developer to design, develop, and deliver informatics solutions that enable our research and preclinical development pipeline. This role focuses on LIMS/ELN platform development, scientific data integrations, and building AI-powered capabilities that accelerate scientific workflows. The ideal candidate brings a data-first perspective — approaching every problem by understanding the underlying data, its structure, and how it flows across systems before writing code. You will serve as a technical lead — driving architecture decisions, mentoring team members, and delivering high-quality solutions on COTS platforms including Sapio, Benchling, and Dotmatics.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Own the design and development of server-side plugins, integrations, and workflows on LIMS/ELN platforms (Sapio preferred) using Java and Python</p></li><li><p>Architect and build AI/GenAI-enabled solutions (LLM agents, RAG pipelines, prompt-engineered workflows) to streamline R&pD informatics processes</p></li><li><p>Develop data pipelines and integrations between scientific instruments, LIMS/ELN systems, and enterprise data platforms — owning data modeling, transformation logic, and data quality validation end-to-end</p></li><li><p>Serve as technical lead on projects — defining technical approach, conducting code reviews, and mentoring developers</p></li><li><p>Partner with scientists, lab operations, and product owners to translate scientific requirements into scalable technical solutions</p></li><li><p>Evaluate and implement COTS platform capabilities (Sapio, Benchling, Dotmatics) to enhance out-of-the-box functionality before custom development</p></li><li><p>Design and develop REST APIs, webhooks, and middleware to enable interoperability across R&PD systems</p></li><li><p>Apply a data-first approach to problem-solving — analyze scientific datasets, identify data quality issues, build dashboards and reporting solutions, and translate data insights into actionable recommendations for scientific collaborators</p></li><li><p>Contribute to platform modernization initiatives, including cloud migration and containerized deployments</p></li><li><p>Ensure solutions meet GxP compliance requirements where applicable</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Bioinformatics, Life Sciences, or related field</p></li><li><p>2+ years of work experience in software development supporting life sciences R&D or laboratory informatics</p></li><li><p>Proficiency in Java (server-side development, plugin architectures)</p></li><li><p>Proficiency in Python (scripting, data pipelines, webhooks, automation)</p></li><li><p>Experience with at least one LIMS or ELN platform: Sapio, Benchling, or Dotmatics. Experience with Sapio LIMS/ELN (server-side plugins, workflows, data model configuration) is preferred.</p></li><li><p>Proven experience with AI/GenAI technologies: building LLM-powered agents, prompt engineering, retrieval-augmented generation (RAG), or AI-assisted workflow automation. Experience with AI agent frameworks (LangChain, LlamaIndex, Claude/Anthropic APIs, OpenAI APIs) is preferred.</p></li><li><p>Familiarity with containerization (Docker, Kubernetes) and CI/CD pipelines (Jenkins, GitHub Actions) is a plus</p></li><li><p>Experience with instrument integrations (TetraScience or direct instrument interfaces) is preferred</p></li><li><p>Experience with data analytics and visualization tools (Spotfire, Tableau, Power BI, or Jupyter notebooks) to support data-driven decision-making is a plus</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Supply Network & Capacity Planning Specialist, Advanced Therapies]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49866]]></requisitionid>
    <referencenumber><![CDATA[R49866]]></referencenumber>
    <apijobid><![CDATA[r49866]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49866/staff-supply-network-capacity-planning-specialist-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Staff Supply Network and Capacity Planning Specialist supporting Advanced Therapies, to join our IOPS Supply Chain team, performing global production allocations and analyzing multi-site production capacity to integrate manufacturing-impactful activities and business initiatives. In this role, you will translate global demand requirements into site production and multi-asset allocation plans, drive long-term planning, and serve as a key liaison across CMC Program Management, Regulatory Sciences, Operations, and Finance — while mentoring team members and influencing strategy across the organization. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Translate global demand requirements into site production and multi-asset allocation plans, efficiently identifying, solutioning, and escalating conflicts while developing multiple draft scenarios for leadership consideration</li><li>Build and maintain capacity models to forecast future needs, including product and asset lifecycle management; lead long-term planning efforts to identify and flag potential business risks</li><li>Serve as liaison between CMC Program Management, Regulatory Sciences, Operations, Finance, and Supply Planning to keep plans aligned with program and supply timelines</li><li>Anticipate issues before they materialize and drive solutions to minimize disruption to production and supply; act as primary point of contact for global production data across cross-functional departments</li><li>Influence and set strategy for production-impactful change management efforts, including determining implementation windows to minimize rework, increase efficiency, and maximize business value</li><li>Create, review, and present routine informational reports to cross-functional audiences; identify opportunities to improve communication and collaboration across functional groups and organizational levels</li><li>Act as subject matter expert for assigned programs and areas of specialty; mentor and provide technical and functional guidance to specialists and other team members supporting global production allocations</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Business, Supply Chain Management, Industrial Engineering, Engineering/Science discipline or related field required</li><li>Principal Specialist: 8+ years of experience</li><li>Staff Specialist: 10+ years of experience</li><li>Master's degree (MBA, MS Supply Chain, or life sciences) and/or APICS certification (CPIM, CSCP) or Lean/Six Sigma knowledge is a plus </li><li>Relevant biotech manufacturing or supply chain management experience is a plus</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Director Marketing - HCP (Lung Oncology)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50188]]></requisitionid>
    <referencenumber><![CDATA[R50188]]></referencenumber>
    <apijobid><![CDATA[r50188]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50188/assoc-director-marketing-hcp-lung-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>BUILD OUR FUTURE TOGETHER:</strong></p><p> The Associate Director, US Lung HCP Oncology Marketing is responsible for contributing to and executing on the healthcare professional strategy for the NSCLC indications. This includes customer engagement and non-personal channel strategy as well as operational support and execution of digital and print media tactics, including support and development of selected field-based materials. The Associate Director will partner closely with cross-functional teams to advance the product’s growth, contribute to the brand's financial success, and strengthen its position in market. </p><p><strong>WHEN & WHERE:</strong></p><p>In the Sleepy Hollow, NY office for 4 days a week with 25% travel for business meetings, conferences, etc.</p><p><strong>DISCOVER YOUR ROLE (these are the responsibilities)</strong></p><ul><li>Development and execution of NSCLC customer engagement and non-personal channel strategy</li><li>Lead for development of the NSCLC non-personal promotion strategy, tactical plans and outputs, data triggers, and budgets</li><li>Responsible for creating downstream field-based materials and selected original field-based pieces as identified and needed</li><li>Vendor Management including digital and/or non-personal communications (e-blasts, Rep Triggered emails, CRM, banner ads, etc)</li><li>Non-personal and field team integration planning, as well as point for field communications</li><li>Responsible for collection and reconciliation of budget with HCP and Scientific marketing leads monthly</li><li>Coordination with other indication teams for brand level personal/non-personal and customer engagement strategy, planning, and execution</li><li>Marketing operations for the team including Veeva CRM platform management, print and digital inventory management, and meeting management</li><li>Partner and collaborate with Sales Training to ensure adequate communication and training for the field team on key initiatives</li><li>Work with agency for label updates/new launches for HCP promotional materials including website</li><li>Optimization of the current metrics and measurement plan in conjunction with the analytics and customer insights team</li><li>Review Committee (RC) captain: leading and driving the RC prioritization and meetings for the NSCLC team</li></ul><p><strong>THIS ROLE REQUIRES: </strong></p><ul><li>Bachelor's degree required; MBA preferred</li><li>10+ years of progressive experience in the pharmaceutical/biotech industry</li><li>8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas</li><li>Field experience is preferred</li><li>Demonstrated ability to work effectively and efficiently with team members, and across departments, to ensure consistency and collaboration with strategy</li><li>Strong project and process skills with attention to detail</li><li>Must be proactive and able to prioritize and operate in fast paced environment</li><li>Experience with media planning and creation, developing digital customer engagement and digital engagement plans preferred</li><li>Good problem-solving ability with strong interpersonal skills both internally and externally</li><li>Ability to grasp complex scientific concepts and clinical data</li><li>Excellent ability to present, listen, and communicate clearly with both scientific and commercial stakeholders</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 08:26:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Finance Transformation]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50110]]></requisitionid>
    <referencenumber><![CDATA[R50110]]></referencenumber>
    <apijobid><![CDATA[r50110]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50110/associate-director-finance-transformation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Finance Transformation, is responsible for driving strategic initiatives that improve the effectiveness, scalability, and operational performance of Finance. This role partners with Finance Operations, Shared Services, IT, and business stakeholders to lead process optimization, technology enablement, standardization, and continuous improvement efforts across the organization.</p><p>The Associate Director will identify opportunities to simplify and modernize finance processes, enhance service delivery, strengthen controls, and support enterprise transformation initiatives. Success in this role requires a deep understanding of finance operations, strong leadership capabilities, and experience leveraging key Finance technologies including Oracle Fusion, Hyperion, Tableau, BI Publisher, and other enterprise platforms to improve business outcomes.</p><p><em>This role is based in our Sleepy Hollow, NY office and is required to be on-site 4 days per week.</em></p><p><strong>Key Responsibilities</strong></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><ul><li><p><strong>Finance Operations Leadership:</strong> Leads Finance operational excellence initiatives by driving process standardization, performance improvement, scalability, risk reduction, and service delivery enhancements aligned with business priorities.</p></li><li><p><strong>Process Improvement & Transformation:</strong> Oversees Finance process transformation efforts through continuous improvement, automation, and change management to increase efficiency, controls, and scalability.</p></li><li><p><strong>Technology Enablement:</strong> Partners with Finance and IT teams to optimize and implement enterprise technologies, leveraging automation, AI, and analytics platforms to improve business performance and decision support.</p></li><li><p><strong>Reporting, Analytics & Decision Support:</strong> Delivers actionable financial and operational insights through standardized reporting, data governance, performance metrics, and trend analysis to support strategic decision-making.</p></li><li><p><strong>Stakeholder Management:</strong> Builds and manages cross-functional partnerships, driving collaboration, executive communication, and data-driven recommendations to achieve operational and transformation objectives.</p></li></ul></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p><strong>Qualifications</strong></p><p><strong>Required Qualifications</strong></p><ul><li>Bachelor's degree required in Finance, Accounting, Business Administration, Information Systems, or a related field. MBA preferred.</li><li>10+ years of progressive experience in Finance Operations, Shared Services, Finance Transformation, or related disciplines.</li><li>5+ years of leadership experience managing teams and complex cross-functional initiatives.</li><li>Demonstrated experience leading process improvement, operational excellence, and technology-enabled transformation initiatives.</li><li>Strong understanding of finance processes, controls, and enterprise operations.</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>CPA, CMA, PMP, Lean Six Sigma, or equivalent certification.</li><li>Experience supporting large-scale Finance Transformation or ERP initiatives.</li><li>Knowledge of Oracle Fusion, Hyperion, Tableau, BI Publisher, Power BI, automation platforms, and AI-enabled technologies.</li><li>Experience in global organizations and shared services environments.</li><li>Proven ability to drive measurable operational improvements and business value.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[AP Service Delivery Coordinator]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48262]]></requisitionid>
    <referencenumber><![CDATA[R48262]]></referencenumber>
    <apijobid><![CDATA[r48262]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48262/ap-service-delivery-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are seeking an AP Service Coordinator to join our Finance team. In this role, you will be responsible for day-to-day invoice and credit memo processing within Accounts Payable workflow and ERP systems, supporting vendor management activities, resolving payment-related queries, and ensuring accurate and efficient AP operations. You will work closely with internal stakeholders and external vendors while leveraging automation, standard processes, and accounting fundamentals to deliver high-quality financial services.</p><p><strong>When & where:</strong></p><p><strong>Hyderabad (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li>Process invoices and credit memos through AP workflow and ERP systems using 2-way and 3-way purchase order matching.</li><li>Compile, review, and analyze routine accounts payable transactions to support internal and external business requests.</li><li>Review and reconcile vendor statements, request missing invoices or credit notes, and coordinate resolution of discrepancies with vendors and internal teams.</li><li>Manage accounts payable inquiries, ensuring timely investigation and resolution of vendor and end-user issues.</li><li>Support departmental goals through execution of assigned AP-related activities and process improvements.</li><li>Utilize AP automation tools, accounting principles, and best practices to improve efficiency and accuracy.</li><li>Build and maintain strong working relationships with internal stakeholders and external vendors to facilitate timely issue resolution.</li><li>Provide backup support for AP Coordinator II responsibilities and assist with invoice entry as required.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Accounting, Finance, Commerce, or a related discipline.</li><li>0-2 years of Accounts Payable experience.</li><li>Basic understanding of accounting principles and strong English communication skills.</li><li>Excellent organizational skills with the ability to manage high volumes of work in a fast-paced environment.</li><li>Strong analytical, problem-solving, and attention-to-detail capabilities.</li><li>Ability to adapt quickly to changing priorities and business requirements.</li><li>Strong interpersonal and stakeholder management skills.</li><li>Proficiency in Microsoft Office applications, including Excel, Outlook, Word, and PowerPoint.</li><li>Experience with Oracle ERP systems, document scanning, and invoice workflow systems is preferred.</li><li>Advanced working knowledge of MS Excel and MS Outlook is highly desirable.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Quality Manager GCP - GVP]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50170]]></requisitionid>
    <referencenumber><![CDATA[R50170]]></referencenumber>
    <apijobid><![CDATA[r50170]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50170/temporary-quality-manager-gcp-gvp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Temporary Quality Manager GCP - GVP, supporting our Global Development quality system in a hybrid work model. In this role, you will support quality management system governance, quality event oversight, and continuous improvement activities while collaborating with Global Development functions and quality leaders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. This is a 12 month contract.</p><p><strong>When & where:</strong></p><p>UK, US, or Ireland</p><p>Work model: Remote</p><p><strong>Discover your role:</strong></p><ul><li><p>Engage Global Development stakeholders to drive process improvements, standardization, and regulatory compliance.</p></li><li><p>Manage quality metrics and trend reporting to support continuous improvement.</p></li><li><p>Oversee the Quality Event portfolio and provide subject matter expertise to functional teams.</p></li><li><p>Lead quality data analysis, root cause investigations, and Corrective Action/Preventive Action development.</p></li><li><p>Manage Quality System Metrics, including thresholds, reporting, actions, and effectiveness measures.</p></li><li><p>Facilitate governance meetings and present data on Quality Management System health.</p></li><li><p>Coordinate procedural document reviews and impact assessments across GDQGO.</p></li><li><p>You promote quality culture and strengthen collaboration across Quality Management System elements.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree and 6+ years of healthcare or pharmaceutical industry experience.</p></li><li><p>Experience in Quality Management, Quality Assurance, or Clinical Development roles with Good Clinical Practice and/or Good Pharmacovigilance Practice expertise.</p></li><li><p>Knowledge of Quality Management System oversight, governance, quality event management, and continuous improvement.</p></li><li><p>Experience as a subject matter expert, process owner, or business process owner in a quality-related area.</p></li><li><p>Experience delivering training and presenting quality and regulatory compliance information.</p></li><li><p>Experience supporting or participating in regulatory agency inspections.</p></li><li><p>Experience training, supervising, or mentoring staff.</p></li><li><p>Strong project management, prioritization, organization, and time management skills.</p></li><li><p>Strong communication, presentation, collaboration, and interpersonal relationship skills.</p></li><li><p>Ability to identify process gaps, manage multiple priorities, and apply sound judgment with integrity and attention to detail.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42034]]></requisitionid>
    <referencenumber><![CDATA[R42034]]></referencenumber>
    <apijobid><![CDATA[r42034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42034/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p><strong>When & Where:</strong></p><ul><li>Location: Rensselaer, NY</li><li>Hours: Monday-Friday 8:00am-4:30pm</li></ul><p><strong>Discover Your Role:</strong></p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p><strong>This Role Requires:</strong></p><ul><li>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level:</li><li>HVAC Technician II: AAS with 2+ years or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years or equivalent combination of education and experience</li><li>Solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director GMP Compliance and Inspections]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49889]]></requisitionid>
    <referencenumber><![CDATA[R49889]]></referencenumber>
    <apijobid><![CDATA[r49889]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49889/director-gmp-compliance-and-inspections/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director GMP Compliance & Inspections to join our Quality department, supporting our IOPS Manufacturing site in Limerick. In this role, you will serve as a strategic compliance leader, ensuring regulatory readiness, driving continuous improvement, and coordinating inspection and audit activities to maintain the highest standards of GMP compliance.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Limerick</p></li><li><p>Work model: Onsite, Monday-Friday</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leading compliance assessments and inspection readiness initiatives across the site</p></li><li><p>Monitoring regulatory trends and translating them into actionable improvements</p></li><li><p>Developing tools, processes, metrics, and content repositories to support audit and inspection preparedness</p></li><li><p>Providing expert guidance on quality and regulatory matters to internal teams and external partners</p></li><li><p>Acting as a key liaison with regulatory agencies, customers, and partner quality organisations</p></li><li><p>Supporting regulatory inspections and internal audits, including coordinating responses and managing information requests</p></li><li><p>Benchmarking best practices and driving continuous improvement to maintain a state of inspection readiness at all times</p></li><li><p>Partnering with compliance and quality teams to identify gaps, resolve issues, and strengthen compliance capabilities across operations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Life Sciences or related field, or equivalent combination of education and experience, and a minimum of 12 years experience in a similar role</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Oncology Marketing - Austria, Switzerland  & Portugal]]></title>
    <date><![CDATA[Sat, 22 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47355]]></requisitionid>
    <referencenumber><![CDATA[R47355]]></referencenumber>
    <apijobid><![CDATA[r47355]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47355/senior-manager-oncology-marketing-austria-switzerland-portugal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><div><div><div><div><div><div><div><div><h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><div><div>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Oncology Marketing, DACH & Portugal to join our International Commercial team, supporting our oncology business across Austria, Switzerland, and Portugal in a hybrid work model. In this role, you will develop and deliver brand strategy across international markets while collaborating with Medical Affairs, global teams, agencies, and external partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</div></div><br><div><strong>When</strong> <strong>&</strong> <strong>where:</strong></div><div><div>Austria & Field Based </div></div><br><div><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></div><ul><li><div>Lead local brand marketing plan development and execution.</div></li><li><div>Analyse market dynamics to find opportunities and identify risks.</div></li><li><div>Shape brand strategy aligned with global direction.</div></li><li><div>Partner with Medical Affairs on market approaches.</div></li><li><div>Drive compliant promotional activities across channels.</div></li><li><div>Adapt global materials for local market use.</div></li><li><div>Plan congresses, healthcare professional engagement, and events.</div></li><li><div>You build positive relationships while balancing strategy and execution.</div></li></ul><br><div><strong>This</strong> <strong>role</strong> <strong>requires:</strong></div><ul><li><div>Bachelor’s degree in business, science, or a related field.</div></li><li><div>8-10+ years’ experience in pharmaceutical or biotechnology brand marketing.</div></li><li><div>Strong knowledge of the Austrian and Swiss healthcare markets.</div></li><li><div>Experience managing agencies and external partners.</div></li><li><div>Knowledge of healthcare compliance and promotional regulations.</div></li><li><div>Proficiency in English & German.</div></li><li><div>Willingness to travel approximately 30-40%.</div></li><li><div>Experience in oncology marketing, including immuno-oncology, preferred.</div></li><li><div>Product launch experience preferred.</div></li><li><div>Strong prioritization, relationship-building, and budget management skills.</div></li></ul></div></div></div></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€87,525.00 - €145,875.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 23 Aug 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[PharmD Program Associate - Regulatory Strategy]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50228]]></requisitionid>
    <referencenumber><![CDATA[R50228]]></referencenumber>
    <apijobid><![CDATA[r50228]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50228/pharmd-program-associate-regulatory-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together:</strong> </p></div><div><p>The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles. </p></div><div><p>This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. </p></div><div></div><div><p><strong>When & where:</strong> </p></div><div><ul><li><p><strong>Location:</strong> Tarrytown, NY </p></li><li><p><strong>Travel percentage:</strong> Up to 15% </p></li></ul></div><div></div><div><p><strong>Program Tracks:</strong> <br>The program is comprised of a 24-month rotational experience within one of the following tracks: </p></div><div><ul><li><p>Clinical Operations & Program Management </p></li><li><p>Clinical Sciences </p></li><li><p><strong>Regulatory Strategy </strong></p></li><li><p>Regulatory Labeling & Advertising/Promotion </p></li><li><p>Safety Sciences </p></li></ul></div><div></div><div><p>Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program. </p></div><div></div><p><strong>Regulatory Strategy</strong> – The regulatory associate will support global regulatory planning and execution to support the clinical development, approval, and lifecycle management of pharmaceutical products. This position partners cross-functionality to define innovative regulatory pathways, ensure compliance with global health authority requirements and guidances, and produce and manage timelines and deliverables across multiple programs. The associate will provide strategic input on operations and submissions to global regulatory authorities to enable efficient and successful product development.</p><div></div></div><div><div><p><strong>Discover your role:</strong> </p></div><div><ul><li><p>Drafting documents integral to clinical sites and regulatory submissions </p></li><li><p>Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others </p></li><li><p>Managing third-party vendors and maintaining timelines of key results </p></li><li><p>Developing regulatory strategies for clinical development programs </p></li><li><p>Analyzing safety data to characterize the safety profile of products throughout their development lifecycle </p></li><li><p>Working with program mentors to improve skills to reach professional goals better </p></li><li><p>Opportunities to travel to clinical sites and/or meetings with health authorities </p></li></ul></div><div></div><div><p><strong>This role requires:</strong> </p></div><div><ul><li><p>Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates within a life science related area of study may also be considered. </p></li><li><p>You must have completed your PharmD and/or PhD degree by Summer 2027 </p></li><li><p>Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus </p></li><li><p>Exposure or familiarity with evaluating clinical trials, scientific literature and data </p></li><li><p>You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences You are eligible to work in the U.S. on a permanent basis </p></li></ul></div><div></div><div><p><strong>Application Details:</strong> </p></div><div><p><strong>When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference. </strong></p></div><div></div></div><div><p><strong>Applications Accepted: August 24th, 2026 - September 11th, 2026</strong> <br>For more information on the tracks, program, and interview process, please refer to the brochure. </p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Mountain West]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48154]]></requisitionid>
    <referencenumber><![CDATA[R48154]]></referencenumber>
    <apijobid><![CDATA[r48154]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48154/neurology-account-director-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Mountain West (Minnesota, Iowa, Missouri, Kansas, Idaho, Colorado, New Mexico and Arizona)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - BUFFALO, NY]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48004]]></requisitionid>
    <referencenumber><![CDATA[R48004]]></referencenumber>
    <apijobid><![CDATA[r48004]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48004/medical-account-specialist-ii-neurology-buffalo-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Buffalo]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Buffalo (Metro), NY</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -RIVERSIDE, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48080]]></requisitionid>
    <referencenumber><![CDATA[R48080]]></referencenumber>
    <apijobid><![CDATA[r48080]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48080/medical-account-specialist-ii-neurology-riverside-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Riverside]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Riverside (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - KNOXVILLE, TN]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48023]]></requisitionid>
    <referencenumber><![CDATA[R48023]]></referencenumber>
    <apijobid><![CDATA[r48023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48023/medical-account-specialist-ii-neurology-knoxville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Knoxville]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Knoxville (Metro), TN</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Medical Review]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47767]]></requisitionid>
    <referencenumber><![CDATA[R47767]]></referencenumber>
    <apijobid><![CDATA[r47767]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47767/senior-manager-medical-review/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Pharmacovigilance Medical Review, India to join our Global Patient Safety team, supporting our global development programs and marketed products in a hybrid role. In this role, you will lead the medical review of safety cases to ensure every report is scientifically sound and inspection-ready before health authority submission, while collaborating with triage, pharmacovigilance, risk management, and clinical development partners across India, the US, and the EU. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad (Hybrid)</p><br><h3><strong>Discover your role:</strong></h3><ul><li><p>Act as team lead, owning end-to-end case quality from coding through causality to final company comment</p></li><li><p>Perform and oversee medical review of ICSRs within defined time standards, ensuring accuracy in Argus</p></li><li><p>Author and review case narratives, analysis of similar events, and company causality rationale</p></li><li><p>Code adverse events and medical history using MedDRA in line with global safety standards</p></li><li><p>Partner with triage, PV, risk management, and clinical development teams on inspection-ready documentation</p></li><li><p>Serve as the medical resource for assigned compounds, resolving and escalating complex case issues</p></li><li><p>Drive SOP development, process improvement, and integration of new technologies including AI</p></li><li><p>You mentor Managers and junior reviewers to ensure consistent application of medical and regulatory standards</p></li></ul><br><h3><strong>This role requires:</strong></h3><ul><li><p>MD or MBBS with active registration, or eligibility for registration, with the relevant Indian professional regulatory body</p></li><li><p>Minimum 8–10 years of pharmacovigilance experience with hands-on ICSR medical review, including narrative authoring, causality assessment, and expectedness determination</p></li><li><p>Strong knowledge of ICH E2A, E2B, and E2D guidelines and FDA/EMA pharmacovigilance regulations</p></li><li><p>Proficiency with Argus Safety or an equivalent safety database and MedDRA coding</p></li><li><p>Sound clinical judgment with the ability to assess complex cases and communicate reasoning clearly in writing</p></li><li><p>Experience within global development programs or on marketed products preferred</p></li><li><p>Exposure to AI or generative AI tools in pharmacovigilance or clinical documentation a plus</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, R&D Chemistry, Peptidomimetic Purification]]></title>
    <date><![CDATA[Sun, 21 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48140]]></requisitionid>
    <referencenumber><![CDATA[R48140]]></referencenumber>
    <apijobid><![CDATA[r48140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48140/sr-associate-scientist-rd-chemistry-peptidomimetic-purification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Sr. Associate Scientist (Peptidomimetic Purification), R&D Chemistry </strong></p><p>We are currently seeking a lab-centric peptide purification chemist to join the R&D (Research & Development) Chemistry group. In this position, they will play a key role in Regeneron’s peptidomimetic antibody-conjugate drug discovery capabilities to enable seamless combination with the company’s existing expertise in biologics and novel genetic medicines. The candidate will drive the purification of peptidomimetic payloads and linker payloads for antibody conjugate drug therapeutics across diverse research areas. Cultural fit with the Regeneron cross-functional teams will be a key driver for success. The R&D Chemistry team is primarily composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have a peptide/peptidomimetic purification background and will require a firm understanding of the latest techniques, strategies and instrumentation for HT peptide purification and isolation. We expect they will act as an inspiring and motivating colleague, effective communicator, and strong project team collaborator to help develop novel antibody-conjugated peptidomimetic therapeutics.</p><p><strong> </strong></p><p><strong>Build our future together:</strong></p><ul><li>Actively participate and collaborate in the day-to-day activities of the R&D Chemistry Peptidomimetic purification team.</li><li>Perform mass-triggered HPLC purification of novel peptidomimetic drug modalities, using modern purification instrumentation/detection and techniques</li><li>Troubleshoot and optimize peptide purification methods and enable high throughput purification and isolation.</li><li>Identify new strategies and technologies for peptidomimetic purification to improve on existing Regeneron techniques</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic purification team.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>Discover your role:</strong></p><ul><li>Passion and enthusiasm about the promise of peptidomimetic conjugated, antibody-targeted therapeutics and how peptide purification can enable their generation.</li><li>You enjoy applying and combining traditional methods and novel technologies to develop solutions for purification.</li><li>You are comfortable working in a cross-functional role and excel in a diverse team where egos are checked at the door.</li><li>You want to provide meaningful contributions to the development of an organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li><li>You prefer to work in an organization that is modality agnostic, letting the data determine the best course forward.</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required, Master’s degree preferred in peptide, peptidomimetic, small molecule purification</li><li>Minimum of 5 years of industry experience.</li><li>Extensive hands-on experience of the HPLC purification/detection and method troubleshooting of peptidomimetics</li><li>Hands-on experience with Waters and/or Agilent purifications systems preferred</li><li>Hands-on experience with mass-triggered collection preferred</li><li>Experience with high throughput purification</li><li>Extensive experience running modern purification/isolation equipment and instrumentation </li><li>A track record of success in the field of either peptidomimetics or small molecules purification is required. </li><li>Working collaboratively with both internal and external organizations (e.g., CROs) is essential.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - QC Analyst HPLC]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49030]]></requisitionid>
    <referencenumber><![CDATA[R49030]]></referencenumber>
    <apijobid><![CDATA[r49030]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49030/temp-qc-analyst-hplc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temporary QC Analyst HPLC </strong>to join our <strong>QC Chemistry </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: 12/7</li><li>Location: Raheen, Limerick.</li><li>This is a 12-month contract position.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Gathering data and documenting test results.</li><li>Reviewing test results to ensure compliance with standards and reporting any quality anomalies.</li><li>Complying with all pertinent regulatory agency requirements.</li><li>Maintaining laboratory supplies.</li><li>Conducting testing on in-process, product, stability, and/or research samples.</li><li>Writing and revising control test procedures and SOPs.</li><li>Completing test records and reviewing data.</li><li>Calibrating or verifying calibration of instruments/devices prior to use.</li><li>Interacting with outside customers or functional peer groups.</li><li>Developing new analytical methods and techniques.</li><li>May assist in validation and method transfer of methods.</li><li>May be involved in establishing the transfer of methodology from R&D.</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have current or prior experience working with HPLC in a regulated environment</li><li>You enjoy working a shift pattern.</li><li>Proven ability to work independently or as part of a team.</li><li>You possess strong trouble-shooting and problem solving skills.</li><li>You have strong attention to detail & excellent written and oral skills.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>To be considered for this opportunity you should have a BS/BA in Life Sciences or related field. Minimum of 2 years’ experience in QC. HPLC/UPLC and Empower required. Experience in SE-UPLC, peptide and glycan assay desirable.</li></ul><h3>Thrive today. Grow tomorrow.</h3><h3>#IRELIM #JOBSIEST #LI-Onsite #REGNQC</h3><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Tampa Central]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49126]]></requisitionid>
    <referencenumber><![CDATA[R49126]]></referencenumber>
    <apijobid><![CDATA[r49126]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49126/medical-specialist-i-allergyent-tampa-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tampa]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US</p><p>The MS is responsible for developing strategy and executing tactics within key allergists in the Dermatology and Respiratory therapeutic areas to generate product utilization. The MS will develop strong working relationships with experts and all Allergists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Tampa Central</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Dermatology or Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Precision Medicine Operations]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49774]]></requisitionid>
    <referencenumber><![CDATA[R49774]]></referencenumber>
    <apijobid><![CDATA[r49774]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49774/manager-precision-medicine-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology. In this role, you will be a key driver of precision medicine operational execution partnering with Precision Medicine Strategy Lead (PMSL), clinical study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL), Clinical Laboratory Study Manager (CLSM), and Clinical Laboratory Project Management (CLPM) groups to deliver high-quality samples and data. Through strong cross functional collaboration and operational excellence, you will help ensure biomarker and non-biomarker strategies are executed seamlessly, enabling the translation of innovative science to medicines for patients.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Uxbridge, United Kingdom</p></li><li><p>Work model/flexibility: 3 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Works with project manager and set-up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics</p></li><li><p>Monitor’s acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensure compliance with ICF permissions</p></li><li><p>Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing </p></li><li><p>Work closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries.</p></li><li><p>Oversees Study start up, closeout and overall life-cycle activities for assigned studies at central lab/specialty labs to support all samples and testing</p></li><li><p>Provides input on sample-related section in clinical trial-related (e.g. protocols and ICF) and other supporting documents</p></li><li><p>Works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials.</p></li><li><p>Enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor's degree with a minimum of 8 years of pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams.</p></li><li><p>Minimum of 5 years' experience with Clinical Trials, focus on clinical sample collection</p></li><li><p>Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested.</p></li><li><p>Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Systems Administrator, Manufacturing & Lab Support]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49100]]></requisitionid>
    <referencenumber><![CDATA[R49100]]></referencenumber>
    <apijobid><![CDATA[r49100]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49100/senior-automation-systems-administrator-manufacturing-lab-support/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Systems Administrator to join our IOPS team, providing expertise in the configuration and administration of automated and computerized system software and firmware across our manufacturing and laboratory operations. In this role, you will ensure systems remain in a compliant and validated state — leading projects, driving continuous improvement, and delivering advanced technical support — while collaborating with Manufacturing, Quality Control, Facilities, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Menands, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Configure and maintain cGMP software for process control, monitoring, and testing; manage user access, system security, configuration management, and recipe and method management to meet regulatory requirements</li><li>Determine data backup and archive requirements and configurations to meet defined RTO and RPO targets; design and maintain recovery processes</li><li>Ensure systems remain in a compliant state by processing change control requests including requirement and design specifications, test plans, technical evaluations, and quality risk assessments</li><li>Support and lead system SAT/FAT, validation, and qualification efforts; generate and execute testing and qualification protocols for automated process, monitoring, and testing equipment</li><li>Initiate, author, and review Change Controls, EOEs, NOEs, DNFs, risk assessments, impact statements, and corrective and preventive action plans; lead investigations and root cause analyses for non-compliance issues</li><li>Lead multiple small to medium-sized projects related to corrective action, software performance improvement, and new equipment and software implementation</li><li>Provide advanced technical automation support and troubleshooting to Manufacturing, Quality Control, and Facilities in accordance with established SOPs and departmental practices</li><li>Support system integration with existing platforms such as LIMS and Historian; draft, approve, and follow relevant system software SOPs and policies; identify opportunities for continuous improvement in processes, procedures, and architecture standards</li><li>Direct experience in a pharmaceutical or biopharmaceutical manufacturing facility preferred</li><li>Advanced experience configuring and troubleshooting process control, monitoring, and product release testing systems including design and installation</li><li>Expertise in developing Software Lifecycle Documentation, software design documents, technical evaluations, and test plans for cGMP process equipment following GAMP 5 guidelines</li><li>Current knowledge of cGMP biotech and pharma operations, regulatory and quality policies, procedures, and documentation methods</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>BS/BA in Science, Engineering, or a related field with 5+ years of relevant experience</li><li>May consider equivalent combination of education and experience</li><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Apprentice I - OEM]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49433]]></requisitionid>
    <referencenumber><![CDATA[R49433]]></referencenumber>
    <apijobid><![CDATA[r49433]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49433/apprentice-i-oem/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Apprenticeship Programme – Original Equipment Manufacturing (OEM Apprenticeship)</strong></p><p><strong>Build our future together:</strong></p><p>The Apprenticeship programme is crafted to provide apprentices with the required knowledge, skills, and competence to perform as a qualified craftsperson. Working under the mentorship of expert Technicians, you'll provide support to the site as part of the Facilities team, specialising The Apprenticeship programme is crafted to provide apprentices with the required knowledge, skills, and competence to perform as a qualified craftsperson. Under the mentorship of expert technicians, the Apprentice is primarily responsible for providing a support service to the site as part of the Technical Operations team specializing</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Supporting Facilities, Quality Assurance, Automation, Engineering, Operations, or other areas as needed</p></li><li><p>Installing, testing, servicing, and maintaining a range of engineered equipment</p></li><li><p>Assembling, installing, testing, commissioning, and troubleshooting electrically powered systems</p></li><li><p>Completing scheduled and unscheduled maintenance on plant and equipment</p></li><li><p>Following site Environmental, Health and Safety policies and help maintain an accident-free workplace</p></li><li><p>Documenting maintenance activities to current GxP standards, using both paper-based records and the computerised maintenance system</p></li><li><p>Helping to maintain the physical condition and environment of all areas</p></li><li><p>Supporting continuous improvement, housekeeping, and Lean initiatives</p></li><li><p>Working across all areas of Facilities</p></li><li><p>Helping to develop and improve the apprenticeship programme at Regeneron</p></li><li><p>Ensuring documentation of maintenance activities to current GxP standards both in paper based records and the computerized maintenance system</p></li><li><p>Maintaining the physical condition and environment of all areas</p></li><li><p>Following current good manufacturing practices (cGMPs)</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have a strong technical capability</p></li><li><p>You're interested in engineering and mechanical systems</p></li><li><p>You have strong fixing and problem-solving skills</p></li><li><p>You enjoy hands-on work and adapt easily to changing tasks</p></li><li><p>You're willing to attend off-the-job college phases over three years</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><p>To be considered for this position you should have a Leaving Certificate, including a pass in Maths and a Science or Engineering subject.</p><p><strong>Hourly Rate Year 1 </strong></p><p>€ 14.15</p><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Dermatology Consumer Marketing]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49745]]></requisitionid>
    <referencenumber><![CDATA[R49745]]></referencenumber>
    <apijobid><![CDATA[r49745]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49745/director-dermatology-consumer-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, Dermatology Consumer Marketing (Atopic Dermatitis) will play a critical role in shaping and executing consumer marketing strategy within an increasingly dynamic healthcare, media, and technology landscape. This leader will drive the development of integrated, omnichannel consumer engagement strategies that educate, engage, and activate patients while accelerating brand growth and adherence.</p><p>The individual will oversee strategy and execution across the full consumer ecosystem, including media, digital experiences, CRM, social, influencer, content, in-office materials, and emerging consumer touchpoints across the full consumer journey. They will be responsible for identifying and leveraging evolving consumer discovery behaviors, advances in AI-enabled marketing, and innovative engagement approaches to create differentiated patient experiences and improve marketing effectiveness.</p><p>The ideal candidate is a strategic and digitally fluent marketing leader with deep direct to consumer marketing expertise, a passion for innovation, and a commitment to continuous learning. They possess a strong track record of leading high-performing teams, developing talent, influencing across complex organizations, and translating consumer insights and business data into impactful marketing strategies that drive measurable results.</p><p>This role directly manages consumer marketers and is responsible for building a high-performing team culture through coaching, talent development, succession planning, and fostering an environment of accountability, collaboration, and continuous learning.</p><h3>When & where:</h3><ul><li>Office Based in Sleepy Hollow, NY for 4 days a week with 15% travel expected</li></ul><h3>Discover your role:</h3><ul><li>Lead the development and orchestration of integrated consumer marketing strategies for Atopic Dermatitis (eczema) that support brand objectives and drive patient engagement, education, and activation</li><li>Own the consumer marketing ecosystem across media, digital, social, influencer, CRM, content, websites, and emerging consumer engagement platforms</li><li>Lead indication-level strategic planning and creative development, ensuring executional excellence across the consumer journey</li><li>Partner with media agencies to develop, optimize, and measure omnichannel media strategies spanning traditional and digital channels</li><li>Leverage consumer insights, analytics, market research, business performance data, and market dynamics to identify opportunities and optimize marketing investments</li><li>Develop consumer experience strategies that improve discoverability, engagement, and conversion across evolving search environments, AI-powered information ecosystems, and emerging consumer behaviors</li><li>Manage CRM and personalization strategies to deepen consumer relationships and improve customer engagement across the patient journey</li><li>Identify, evaluate, and pilot emerging marketing technologies, AI-enabled capabilities, and innovative engagement approaches that improve marketing effectiveness and patient experience</li><li>Own agency management, budget stewardship, and operational excellence alongside alliance marketing team to ensure delivery of high-quality marketing initiatives on time and within budget</li><li>Collaborate closely with HCP Marketing, Medical Affairs, Market Research, Analytics, Patient Services, PR, Legal, Regulatory, and Alliance partners to deliver aligned and integrated customer experiences</li><li>Lead, coach, and develop a high-performing team while fostering a culture of innovation, accountability, and continuous improvement</li><li>Serve as a consumer marketing thought leader across the Dermatology franchise by sharing best practices, emerging trends, and scalable marketing capabilities that can be leveraged across indications</li><li>Partner across Dermatology brands to identify opportunities for consistency, capability-building, and adoption of innovative consumer marketing approaches</li><li>Ensure all strategies, tactics, and materials comply with corporate, legal, regulatory, and industry requirements</li></ul><h3>This role requires:</h3><ul><li>12+ years of progressive consumer marketing, brand marketing, digital marketing, or related commercial experience in pharmaceutical marketing, including experience leading integrated marketing strategies</li><li>5+ years of people leadership experience with demonstrated success developing high-performing teams and future leaders</li><li>Pharmaceutical, biotech, healthcare, or highly regulated industry experience required</li><li>Demonstrated expertise in direct-to-consumer marketing, digital transformation, omnichannel engagement, and marketing innovation</li><li>Dermatology, Immunology, or specialty biologics experience preferred</li><li>Experience operating within alliance or co-promote partnerships preferred</li><li>Bachelor's degree required; MBA or advanced degree preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Financial Analyst, SOX Compliance]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47488]]></requisitionid>
    <referencenumber><![CDATA[R47488]]></referencenumber>
    <apijobid><![CDATA[r47488]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47488/senior-financial-analyst-sox-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Senior Financial Analyst, SOX Compliance</strong></p><p>Do you enjoy turning complex financial controls into clear, practical guidance that helps teams move faster? As our Senior Financial Analyst, SOX Compliance, you'll be the go-to expert connecting Program Finance with our Global Development organization, making sure our clinical trial finances run smoothly, transparently, and in full compliance with SOX requirements. You'll build and refine the tools, processes, and guidelines that keep our financial operations efficient, audit-ready, and aligned with how the business actually works.</p><br><h3><strong>What You'll Do:</strong></h3><ul><li>Ensure financial controls are executed in line with the Company's SOX requirements.</li><li>Partner with the Head of Program Finance to present process changes to the SOX Committee and keep SOX documentation (narratives) current.</li><li>Lead the annual SOX audit process — running walkthroughs with internal and external auditors and preparing documentation for Study Budget and Study Requisition approvals as part of key controls testing.</li><li>Advise Program Finance and Global Development teams on SOX key controls for Study Budget and Study Requisition approvals.</li><li>Conduct ad-hoc reviews of Program Trial Finance (PTF) analysts' documentation, spotting gaps or weaknesses and recommending improvements to strengthen controls.</li><li>Champion operational improvements that cut unnecessary work and streamline processes — always within SOX guardrails.</li><li>Take a continuous-improvement mindset to clinical trial, program budget, and study-level requisition processes, including:</li><li>Submitting and updating approved budget information in Hyperion.</li><li>Reviewing budget dashboards to confirm accurate reporting of approved budgets.</li><li>Reviewing custom hierarchies for clinical trials and required approvers.</li><li>Administering and maintaining study budget approval workflows and QlikView dashboards that support SOX compliance via partnership with IT support teams.</li><li>Periodically reviewing budget values in Hyperion to keep QlikView budget dashboards accurate and up to date.</li></ul><br><h3><strong>What You'll Bring:</strong></h3><ul><li>Strong verbal and written communication skills, with the ability to engage confidently with business partners and leaders at all levels.</li><li>A track record of managing multiple projects in a fast-paced environment.</li><li>Sharp problem-solving, quantitative, and analytical abilities.</li><li>Experience working within a rapidly growing organization.</li><li>Excellent organization and attention to detail, with the ability to work independently and see tasks through efficiently.</li><li>Strong analytical skills and a knack for turning findings into practical solutions and process improvements.</li></ul><br><h3><strong>This Role Requires:</strong></h3><ul><li>Bachelor's degree in Finance, Accounting, or a related quantitative field; an MBA is a plus.</li><li>5+ years of experience in compliance, forecasting, budgeting, and/or business partnering — ideally within a science- or research-driven organization.</li><li>A proven track record spanning both audit and finance functions.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager, Predictive Analytics]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48512]]></requisitionid>
    <referencenumber><![CDATA[R48512]]></referencenumber>
    <apijobid><![CDATA[r48512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48512/senior-product-manager-predictive-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are seeking a highly motivated and skilled Senior Product Manager to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop products based on the world’s largest integrated datasets of genomics, proteomics, and electronic medical records. </p><p>The role involves partnering with cross-functional teams, including Business Development, Laboratory staff, and other scientific groups, to foster collaboration and advance key initiatives. Excellent communication and interpersonal skills are also required as this candidate will be encouraged to work efficiently in a collaborative, team working environment.</p><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Mock up products based on proteomic, electronic medical record, and/or genomic datasets</p></li><li><p>Draft specifications for software to display disease risk predictions, use AI tools to implement the specifications, and evaluate the results</p></li><li><p>Turn disease prediction ideas from other teams and collaborators into concrete project/budget proposals</p></li><li><p>Stay informed on emerging market trends in disease prediction and applications of genomics data to continuously refine product directions</p></li><li><p>Deliver clear and concise presentations of genomics and proteomic use cases to leadership, ensuring alignment with organizational goals and priorities</p></li><li><p>Assist in the design of clinical validation programs for products</p></li><li><p>Leader partner and customer discussions to test hypotheses about the value of new products, and summarize this feedback to leadership </p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>A bachelor's degree in a relevant field (software engineering, computational biology, etc.) with at least 13+ years of relevant industry experience (or a PhD and +7 years of experience as an equivalent)</p></li><li><p>Demonstrated expertise in software engineering or product design </p></li><li><p>Proven skills for translating scientific results into product prototypes</p></li><li><p>Proven track record to independently lead and run research projects from conception to completion.</p></li><li><p>Excellent communication and collaboration skills, with a track record of working effectively in interdisciplinary teams</p></li><li><p>Proven ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Immuno Assay]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46562]]></requisitionid>
    <referencenumber><![CDATA[R46562]]></referencenumber>
    <apijobid><![CDATA[r46562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46562/senior-associate-scientist-immuno-assay/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Associate Scientist to join our team, supporting our pipeline in a hybrid work mode. In this role, you will develop and validate immunoassays while collaborating with Assay Development Group scientists and study directors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Tarrytown, New York</p><p>On-site<br> </p><p><strong>Discover your role:</strong></p><ul><li>Design, execute, and troubleshoot immunoassays, including enzyme-linked immunosorbent assays, with minimal supervision.</li><li>Develop immunoassay methods and write validation protocols for study director review.</li><li>Perform validation experiments and prepare tabular results, reports, and procedure documents.</li><li>Process samples, run assays, and analyze data under current GxP guidance.</li><li>Evaluate new immunoassay technologies, formats, and techniques.</li><li>Operate laboratory instruments and oversee verifications or maintenance when required.</li><li>Oversee reagent preparation, laboratory supplies, cleanliness, and safety compliance.</li><li>You manage multiple projects and clearly present results through reports or presentations.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in biology or a related field and three to six years of experience.</li><li>Hands-on immunoassay knowledge using multiple detection systems.</li><li>Understanding of methodologies measuring proteins and immunogenicity.</li><li>Knowledge of Good Laboratory Practice, FDA regulations, and company standard operating procedures.</li><li>Prior bioanalytical assay development experience is highly desirable.</li><li>Master’s degree is preferred.</li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro)-Louisville, KY]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49298]]></requisitionid>
    <referencenumber><![CDATA[R49298]]></referencenumber>
    <apijobid><![CDATA[r49298]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49298/medical-specialist-i-gastro-louisville-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Louisville-Jefferson County5]]></city>
    <state><![CDATA[Kentucky]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where:</strong></p><p>Field Role</p><p>Location: Louisville, KY</p><p><strong>Discover your role:</strong></p><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Gastroenterology market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Osaka Area]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49518]]></requisitionid>
    <referencenumber><![CDATA[R49518]]></referencenumber>
    <apijobid><![CDATA[r49518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49518/medical-representative-mr-dermatology-starosaka-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Sales Representative Dermatology Japan Region to join our commercial team, supporting Japan in a field-based work mode. In this role, you will achieve dermatology sales objectives and deliver customer value while collaborating with sales leadership, marketing teams, and alliance partners. This position offers the opportunity to supply to a fast-growing, science-driven organization making a relevant difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Osaka, Japan</p><p>Work model: Field-based</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Achieve dermatology sales objectives through territory budget management.</li><li>Develop and update annual territory business plans using market insights.</li><li>Build territory action plans using key data sources.</li><li>Deliver disease-focused customer engagement and value-based solutions.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Partner with alliance teams to achieve shared business objectives.</li><li>Follow regulatory, legal, and company compliance requirements.</li><li>You act strategically and lead priorities to enhance customer impact.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree or equivalent.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Valid driver license and MR Certification.</li><li>Strong customer engagement skills with a focus on delivering value.</li><li>Technical proficiency and ability to conduct disease and concept selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and audience-focused communication skills.</li><li>Ability to implement strategic and tactical plans independently under tight timelines.</li><li>Computer proficiency in word processing, spreadsheets, databases, and email software.</li><li>Alliance partnership experience.</li><li>Dermatology knowledge and biologics sales experience preferred.</li><li>Current clinical knowledge of relevant therapy areas and competitor brands preferred.</li><li>Established Key Opinion Leader relationships within dermatology preferred.</li><li>English fluency is a plus.</li><li>Willingness to travel and work evenings or weekends when required.</li><li>Dedication to training completion, safe driving practices, and company policies.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Medical Affairs, Hematology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49776]]></requisitionid>
    <referencenumber><![CDATA[R49776]]></referencenumber>
    <apijobid><![CDATA[r49776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49776/director-medical-affairs-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director Medical Affairs Hematology Strategy Japan to join our Global Medical Affairs team, supporting our Japan business in a hybrid work model. In this role, you will provide scientific and medical leadership for our hematology portfolio and pipeline while collaborating with global, regional, local, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Tokyo</li><li>Work model: Hybrid</li></ul><br><h3>Discover your role:</h3><ul><li>Serve as the in-country medical lead for hematology assets and pipeline activities.</li><li>Represent Medical Affairs in cross-functional planning with regional and global partners.</li><li>Direct Field Medical execution, insight generation, and external scientific engagement.</li><li>Coach and develop Field Medical colleagues through onboarding, feedback, and guidance.</li><li>Support clinical development, research, investigator engagement, and site identification.</li><li>Lead medical strategy for congresses, symposia, advisory boards, and educational activities.</li><li>Deliver scientific presentations to healthcare professionals and key stakeholders.</li><li>You build trusted relationships and bring local patient and physician insights forward.</li></ul><br><h3>This role requires:</h3><ul><li>MD or PhD with strong scientific expertise and extensive hematology experience.</li><li>More than 10-15 years of relevant pharmaceutical or biotechnology industry experience.</li><li>Strong knowledge of Medical Affairs, Clinical Development, and Japan regulatory requirements.</li><li>Solid experience in drug development and lifecycle management.</li><li>Experience leading people and directing Field Medical activities.</li><li>Deep knowledge of solid tumors; immuno-hematology experience preferred.</li><li>Experience in matrix organizations and cross-functional collaboration.</li><li>Thorough understanding of the Japanese healthcare environment.</li><li>Ability to shape strategic and tactical planning opportunities.</li><li>Excellent medical communication, analytical, and stakeholder management skills.</li><li>Publication record and translational or basic research experience are a plus.</li><li>Business-level Japanese and English proficiency.</li><li>Ability to manage multiple priorities while maintaining compliance standards.</li><li>Willingness to travel approximately 10-20%.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Accountant, Corporate Accounting]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47371]]></requisitionid>
    <referencenumber><![CDATA[R47371]]></referencenumber>
    <apijobid><![CDATA[r47371]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47371/staff-accountant-corporate-accounting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Join Regeneron's Corporate Accounting team as a Staff Accountant with high visibility across Product Revenue and general ledger accounting. This role owns core close-process responsibilities — journal entries, account reconciliations, and variance analysis — and works directly with Accounting, Finance, Commercial, and Trade on GAAP-based accounting for the business.</p><p>We are looking for a Staff Accountant who is a collaborative team member, communicates effectively with colleagues, thrives in a dynamic environment, and is eager to take on challenges and contribute to Regeneron's growth.</p><p><strong>Discover your role:</strong></p><ul><li>Perform Product Revenue accounting activities, including journal entries for sales, gross to net deductions, and receivables; balance sheet reconciliations; and detailed trend analysis of product sales related deductions</li><li>Own preparation and analysis of Corporate Accounting schedules and balance sheet account reconciliations for assigned areas ensuring completeness, accuracy, and timely resolution of reconciling items</li><li>Partner with Finance to ensure completeness and accuracy of accruals and reclasses</li><li>Participate in the Oracle Fusion Cloud Financials ERP implementation and ongoing optimization efforts, including user acceptance testing (UAT), process design activities, updates to process documentation, and identification of automation opportunities</li><li>Support accounting transformation and process improvement initiatives by leveraging technology, automation, and data analytics to improve reporting and operational efficiency</li><li>Analyze financial results, investigate period-over-period fluctuations, and prepare meaningful variance explanations for Management</li><li>Maintain knowledge of and compliance with Company accounting policies and internal controls</li><li>Ensure compliance with the Company’s Prepaid Expense Accounting Policy and other relevant accounting policies</li><li>Support compliance with Sarbanes Oxley (SOX) requirements, including maintaining documentation and supporting control execution and assist with internal and external audit requests</li><li>Assist with special projects, financial analyses, and continuous improvement initiatives</li></ul><p><strong>This Role May Be for You If You:</strong></p><ul><li>Bachelors degree in Accounting or Finance. CPA or active pursuit of CPA licensure is preferred.</li><li>Have 1-3 years of general ledger accounting, audit, or corporate accounting experience within public accounting experience (Big 4 or national firm) and/or publicly traded company environment are considered strong assets.</li><li>Experience with ERP systems, financial reporting tools, and large datasets is preferred. Experience with Oracle GL, Oracle Fusion, SmartView, Hubble, or similar reporting tools is a plus.</li><li>Are a team player who collaborates effectively, thinks independently, and proactively proposes solutions with a continuous improvement mindset</li><li>Have a solid grasp of GAAP and enjoy applying it to real operational challenges</li><li>Are analytical and comfortable working with large data sets to reach sound accounting conclusions</li><li>Bring strong organizational skills and attention to detail</li><li>Can operate in a fast‑paced environment and comfortably manage multiple priorities</li><li>Have strong written and verbal communication skills</li><li>Enjoy partnering with cross-functional teams and learning how accounting supports business decision-making</li><li>Have an interest in leveraging technology, automation, and data analytics to improve accounting processes</li><li>Are seeking opportunities for professional growth, expanded responsibilities, and career progression within Finance and Accounting</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Precision Medicine (Clinical Diagnostics)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49845]]></requisitionid>
    <referencenumber><![CDATA[R49845]]></referencenumber>
    <apijobid><![CDATA[r49845]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49845/associate-director-precision-medicine-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution. This role owns CDx programs from early biomarker feasibility through clinical validation, regulatory submission, and launch — translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions. You'll work at the interface of biomarker science, clinical development, regulatory, and external IVD partners to ensure diagnostics keep pace with therapeutic milestones. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Armonk, NY, Cambridge, MA, Warren, NJ</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles (TPPs), defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays). </p></li><li><p>Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics.</p></li><li><p>Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints. </p></li><li><p>Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. </p></li><li><p>Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. </p></li><li><p>Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment. </p></li><li><p>Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). </p></li><li><p>Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. </p></li><li><p>Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. </p></li><li><p>8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. </p></li><li><p>Track record translating biomarker science into validated assays supporting drug approvals. </p></li><li><p>Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). </p></li><li><p>Ability to translate complex scientific and clinical data for cross-functional and executive audiences. </p></li><li><p>Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Continuous Improvement Specialist]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49070]]></requisitionid>
    <referencenumber><![CDATA[R49070]]></referencenumber>
    <apijobid><![CDATA[r49070]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49070/staff-continuous-improvement-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a<strong> Staff Continuous Improvement Specialist </strong>to join our Continuous Improvement team. In this role, you will accountable for driving targeted, measurable, and sustainable improvements in Safety, Quality, Delivery, Cost, and People (SQDCP) performance by owning key transformational initiatives and deploying CI systems and tools across the site.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Raheen, Limerick.</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Owning the technical performance and results of key transformational projects (e.g. visual and daily management systems or equivalent site-wide initiatives); working with site leadership to set priorities and translate strategy into actionable plans</p></li><li><p>Evaluating and prioritising the CI project portfolio against strategic goals, and designs, executes, and project manages significant initiatives aligned to IOPS Strategic Priorities</p></li><li><p>Tracking and reporting the impact of CI initiatives against SQDCP metrics (Safety, Quality, Delivery, Cost, People)</p></li><li><p>Independently facilitates cross-site / cross-functional Kaizens and structured problem-solving activities that eliminate waste, finding alternative solutions and obtaining buy-in even amid resistance or ambiguity</p></li><li><p>Developing new CI systems, tools, and training, and managing their upskilling and deployment across IOPS</p></li><li><p>Providing dedicated CI support to a specific organisational group within IOPS, building and sustaining strong relationships with senior leaders and key influencers across functions, and helps the team map who to engage for what, strengthening the team's organisational reach</p></li><li><p>Preparing and presenting influential reports and proposals to project teams and senior management, tailoring communication style and format to the audience</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BSc/BA in a scientific, engineering, or business discipline required (MS/MBA preferred), with 10+ years of relevant experience in operations, manufacturing, or a related field, including demonstrated experience in a highly regulated (e.g., GMP) environment</p></li><li><p>Principal Specialist: BSc/BA plus 8 years experience</p></li></ul><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLCI</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €120,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Engineer]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49773]]></requisitionid>
    <referencenumber><![CDATA[R49773]]></referencenumber>
    <apijobid><![CDATA[r49773]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49773/project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><strong>Build our future together:</strong></div><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Project Engineer </strong>to join our <strong>Project Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Designing and specifying cGMP process equipment, piping, and/or controls</p></li><li><p>Managing small projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li><li><p>Preparing process and instrument drawings and other related drawings</p></li><li><p>Developing Process Flow Diagrams for manufacturing processes.</p></li><li><p>Supporting the validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Assisting in investigations of process equipment and control system anomalies</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations for and executes modification change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>Problem-solving and continuous improvement skills</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>To be considered for this opportunity you should have a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li><li><p><strong>Senior Project Engineer:</strong> BS/BEng or higher in chemical/process/mechanical engineering with 5+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager - Hematology (f/m/d) - Germany North-West]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49846]]></requisitionid>
    <referencenumber><![CDATA[R49846]]></referencenumber>
    <apijobid><![CDATA[r49846]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49846/key-account-manager-hematology-fmd-germany-north-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hematology to join our International Hematology team, supporting Germany in a field-based work mode. In this role, you will drive account performance and regional contracting activities for our hematology portfolio while collaborating with Medical colleagues, pharmacists, hospital stakeholders, and commercial teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Field-based in Germany North-West</p><p><strong>Discover your role:</strong></p><ul><li><p>Establish high-quality healthcare professional relationships across the territory</p></li><li><p>Develop referral networks spanning hospital, outpatient, and office-based settings</p></li><li><p>Deliver portfolio value messages through face-to-face, remote, and digital engagement</p></li><li><p>Partner with Medical on regional programs and healthcare professional activities</p></li><li><p>Manage account planning, segmentation, targeting, and local account plans</p></li><li><p>Support regional contracting activities and adapt contract models to local needs</p></li><li><p>Analyze market trends and competitor activity to inform negotiations</p></li><li><p>Thrive in an agile environment and adjust priorities to account needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or recognized equivalent for sales professionals</p></li><li><p>5-7 years of progressive pharmaceutical or biotechnology sales experience</p></li><li><p>Knowledge of the German healthcare system and regional market structures</p></li><li><p>Experience using data, customer relationship management systems, and multiple business systems</p></li><li><p>Qualification in applicable pharmaceutical industry codes, including EFPIA Code or VFA Pharmakodex</p></li><li><p>Fluency in German and good working knowledge of English</p></li><li><p>Ability to manage a large territory independently with frequent travel</p></li><li><p>Strong customer engagement, negotiation, and communication skills</p></li><li><p>High integrity and ethical standards in all interactions</p></li><li><p>Hematology sales experience and an established network strongly preferred</p></li><li><p>Experience supporting hospital, purchasing group, or payer contract negotiations preferred</p></li><li><p>Product launch experience preferred</p></li></ul><p>Salary range (annually)</p><p>73,125 -121,875 €</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist-Raleigh & Durham, NC]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49458]]></requisitionid>
    <referencenumber><![CDATA[R49458]]></referencenumber>
    <apijobid><![CDATA[r49458]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49458/oncology-account-specialist-raleigh-durham-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Raleigh & Durham, NC</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC experience Preferred).</p></li><li><p>Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC thought leaders or high influence customers in group practices, academic hospitals, key institutions.</p></li><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines.</p></li><li><p>You are results oriented with a track record of success with product launches.</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49912]]></requisitionid>
    <referencenumber><![CDATA[R49912]]></referencenumber>
    <apijobid><![CDATA[r49912]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49912/director-international-commercialization-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Uxbridge, UK - multiple locations are being considered for this role</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs - Hematology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49777]]></requisitionid>
    <referencenumber><![CDATA[R49777]]></referencenumber>
    <apijobid><![CDATA[r49777]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49777/senior-manager-field-medical-affairs-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Field Medical Hematology Japan to join our Global Medical Affairs team, supporting our Hematology business area in a field-based work model. In this role, you will advance scientific engagement, generate actionable field insights, and support Medical Affairs execution while collaborating with Medical Affairs colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Japan</p><p>Work model: Field-based</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead compliant scientific engagement with external experts across Hematology.</li><li>Gather and communicate field insights from clinical practice and congress activities.</li><li>Own complex field medical activities aligned with Medical Affairs strategy.</li><li>Maintain expert, investigator, and engagement-priority mapping.</li><li>Deliver disease-state education to practitioners and researchers in Hematology.</li><li>Contribute to evidence generation, medical education, and scientific communication.</li><li>Lead selected Medical Affairs projects and support IIS and clinical-trial activities.</li><li>You build trusted relationships and translate scientific exchange into actionable insights.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>MD, PhD, or PharmD preferred; Master's degree with substantial Hematology experience may be considered.</li><li>Deep scientific expertise in Hematology and solid tumors; hemato-oncology or immuno-Hematology experience preferred.</li><li>6+ years in pharmaceutical, clinical research, clinical practice, Medical Affairs, or related scientific roles.</li><li>Ability to independently deliver advanced scientific engagement and high-quality field outcomes.</li><li>Strong scientific communication and presentation skills with external and internal stakeholders.</li><li>Experience building relationships with academic and clinical experts.</li><li>Experience working in matrix organizations; partnership experience is valued.</li><li>Understanding of compliance requirements governing non-promotional Field Medical activities.</li><li>Experience supporting evidence generation, medical education, scientific communication, or Medical Affairs projects preferred.</li><li>Prior Field Medical or Medical Science Liaison experience in Hematology preferred.</li><li>Fluency in Japanese and English.</li><li>Ability and willingness to travel approximately 40–60%.</li><li>Strong teamwork, integrity, ownership, judgment, adaptability, and follow-through.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 14 Aug 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Compliance Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49352]]></requisitionid>
    <referencenumber><![CDATA[R49352]]></referencenumber>
    <apijobid><![CDATA[r49352]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49352/qa-compliance-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> QA Compliance Specialist </strong>to join our <strong>QA Compliance & Quality Systems </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Supporting the administration, review, and coordination of Change Control records to ensure compliance with company procedures and regulatory requirements.</li><li>Providing quality oversight of Change Control activities throughout the change lifecycle, including initiation, impact assessment, implementation, effectiveness verification, and closure.</li><li>Reviewing and approving Quality System documentation, including: Change Control records, Deviation investigations, CAPA records, Risk assessments, Standard Operating Procedures and Work Instructions and associated quality documentation.</li><li>Collaborating with Manufacturing, Quality Control, Engineering, Validation, Supply Chain, MSAT, and other functional areas to ensure appropriate assessment and implementation of proposed changes.</li><li>Ensuring Change Controls are appropriately categorised, documented, assessed for impact, and progressed in accordance with established timelines.</li><li>Supporting quality system governance activities, including monitoring open records, escalating risks, and driving timely completion of actions.</li><li>Assisting in the generation, monitoring, and trending of Quality System metrics to support management review and continuous improvement initiatives.</li><li>Participating in investigations related to Change Controls and supporting identification and implementation of corrective and preventive actions where required.</li><li>Supporting the development and delivery of training on Change Control and Quality System processes.</li><li>Actively participating in continuous improvement initiatives to enhance Quality System effectiveness, compliance, and efficiency.</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Experience working with Quality Systems, including one or more of the following: Change Controls, Deviations, CAPA's, Audit Management and Risk Management</li><li>Working knowledge of cGMP requirements and regulatory expectations.</li><li>Strong organisational, communication, and stakeholder management skills, with the ability to effectively coordinate activities across multiple functional areas.</li><li>Biologics manufacturing experience desirable.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or a related discipline.</li><li>Requires 3-5+ years of relevant experience in the pharmaceutical, biotechnology, or other regulated industry.</li><li>Relevant experience may be considered in lieu of educational requirements.</li></ul><h3>Thrive today. Grow tomorrow.</h3><p>#IRELIM #JOBSIEST #LI-Onsite #REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager QA Operations]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49368]]></requisitionid>
    <referencenumber><![CDATA[R49368]]></referencenumber>
    <apijobid><![CDATA[r49368]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49368/manager-qa-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager / Sr Manager QA Operations </strong>to join our <strong>QA Operations Batch Review</strong> team. In this role, you will be responsible for the management and oversight of the QA Operations function.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Directing and continuously improving QA Operations processes ensuring that performance and quality conform to regulatory standards and internal requirements</p></li><li><p>Driving initiatives that support departmental growth and organizational objectives to improve processes, reduce waste and improve efficiency</p></li><li><p>Providing leadership and collaboration within and across the organization at all levels, across functional groups</p></li><li><p>Partnering with US counterparts to ensure global alignment of processes, systems and procedures, unified communication to user areas, and identification of system enhancements</p></li><li><p>Identifying risks to operations and collaborating with the team and business to identify and implement mitigations</p></li><li><p>Ensuring appropriate resourcing for document schedule planning adherence</p></li><li><p>Developing resourcing strategies to plan and manage the operating budget and headcount budget and forecasting to ensure maximum utilization of personnel to fulfill department objectives</p></li><li><p>Defining and implementing quality standards, systems, and metrics for QA Operations to ensure performance, compliance, effectiveness, efficiency, and value to the business in line with department goals</p></li><li><p>Reporting the status of process performance and ensuring that they are on-time and accurate metrics for presentation</p></li><li><p>Site support for QA Operations global teams, projects, and initiatives; continuously partnering with counterpart site leads</p></li><li><p>Involved in Regulatory Agency interactions and preparation as related to site inspections and ensuring regulatory observations in their area are adequately addressed and completed on schedule</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Requires BSc/BEng in scientific discipline or related field with 8+ years’ experience in a pharmaceutical/biologics manufacturing environment desired or equivalent combination of education and experience</p></li><li><p>Sr Manager: BSc/BEng plus 10+ years' experience</p></li></ul><p><strong>#IRELIM #JOBSIEST #LI-Onsite </strong> <strong>#REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€74,000.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Hematology Thought Leader Liaison (Midwest)]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48325]]></requisitionid>
    <referencenumber><![CDATA[R48325]]></referencenumber>
    <apijobid><![CDATA[r48325]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48325/associate-director-hematology-thought-leader-liaison-midwest/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Michigan]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Hematology Thought Leader Liaison (TLL), Midwest is a field-based, non-sales position on Regeneron’s Commercial Hematology Marketing team. It will be focused on enhancing and improving interactions with key external US hematology thought leaders at academic centers and leading community practices for our Hematology bispecific.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Oncology/Hematology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><h3>When & where:</h3><ul><li>Must reside in one of the following states:</li><li>North Dakota, South Dakota, Nebraska, Minnesota, Iowa, Michigan, Wisconsin, Ohio, Indiana, and Kentucky</li><li>Must be able to travel 60%-80% of time within the territory</li></ul><h3>Discover your role:</h3><ul><li>The Hematology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau program placement and execution, which may include identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10 years of work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in hematology/oncology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry</li><li>Experience with physician-administered biologics preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 09:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[PharmD Program Associate - Regulatory Labeling & Advertising/Promotion]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50229]]></requisitionid>
    <referencenumber><![CDATA[R50229]]></referencenumber>
    <apijobid><![CDATA[r50229]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50229/pharmd-program-associate-regulatory-labeling-advertisingpromotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> </p><p>The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles. </p><p>This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. </p><p><strong>When & where:</strong> </p><ul><li><p><strong>Location:</strong> Tarrytown, NY </p></li><li><p><strong>Travel percentage:</strong> Up to 15% </p></li></ul><p><strong>Program Tracks:</strong> <br>The program is comprised of a 24-month rotational experience within one of the following tracks: </p><ul><li><p>Clinical Operations & Program Management </p></li><li><p>Clinical Sciences </p></li><li><p>Regulatory Strategy </p></li><li><p><strong>Regulatory Labeling & Advertising/Promotion</strong> </p></li><li><p>Safety Sciences </p></li></ul><p>Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program. </p><p><strong>Regulatory Labeling & Advertising/Promotion </strong>– Associate will contribute to the development of labeling content and labeling strategies through interpretation of regulations and guidelines; and support the labeling process throughout the product lifecycle, including Labeling Working Group reviews and management approvals. The associate will also develop knowledge and skills to interpret FDA regulations and guidances to ensure promotional communications are truthful and not misleading, and appropriately advise teams on associated regulatory risks, and support FDA-Office of Prescription Drug Promotion (OPDP) interactions.</p><p><strong>Discover your role:</strong> </p><ul><li><p>Drafting documents integral to clinical sites and regulatory submissions </p></li><li><p>Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others </p></li><li><p>Managing third-party vendors and maintaining timelines of key results </p></li><li><p>Developing regulatory strategies for clinical development programs </p></li><li><p>Analyzing safety data to characterize the safety profile of products throughout their development lifecycle </p></li><li><p>Working with program mentors to improve skills to reach professional goals better </p></li><li><p>Opportunities to travel to clinical sites and/or meetings with health authorities </p></li></ul><p><strong>This role requires:</strong> </p><ul><li><p>Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates within a life science related area of study may also be considered. </p></li><li><p>You must have completed your PharmD and/or PhD degree by Summer 2027 </p></li><li><p>Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus </p></li><li><p>Exposure or familiarity with evaluating clinical trials, scientific literature and data </p></li><li><p>You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences You are eligible to work in the U.S. on a permanent basis </p></li></ul><p><strong>Application Details:</strong> </p><p><strong>When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference.</strong> </p><p><strong>Applications Accepted: August 24th, 2026 - September 11th, 2026</strong> <br>For more information on the tracks, program, and interview process, please refer to the brochure. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director, Clinical Program Lead, Hematology Oncology]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47077]]></requisitionid>
    <referencenumber><![CDATA[R47077]]></referencenumber>
    <apijobid><![CDATA[r47077]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47077/executive-medical-director-clinical-program-lead-hematology-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Medical Director to join our Hematology team, providing overall clinical scientific leadership for our cell therapy program. In this role, you will shape clinical development strategy and drive execution of clinical trials while collaborating closely with the Global Program Head, Research, Early Clinical Development, Global Medical Affairs, Marketing, and HEOR. You'll serve as a clinical role model, bringing outstanding scientific knowledge to hematology research and leading a team of MDs and clinical scientists, reporting directly to the VP, Therapeutic Area Lead, Hematology.</p><p>This position offers the opportunity to provide clinical scientific leadership on a fast-growing, science-driven cell therapy program making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Travel: 10%, to relevant conferences/congresses</p></li></ul><p><br><strong>Discover your role:</strong></p><ul><li><p>Acts as medical expert and leader with external collaborators (regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal partners across Research, Global Medical Affairs, and Marketing</p></li><li><p>Builds and defends data-driven clinical strategies with scientific rigor and creative problem-solving, both internally and with external partners</p></li><li><p>Designs innovative First-in-Human and Phase 2/3 programs that are smaller yet robust, shortening development timelines amid an evolving regulatory landscape</p></li><li><p>Drives consensus across multi-disciplinary, matrixed clinical teams in a fast-paced, hands-on environment</p></li><li><p>Partners closely with the Global Program Head to define the optimal development strategy for the cell therapy portfolio</p></li><li><p>Leads and develops a team of MDs and clinical scientists to meet personal and business goals</p></li><li><p>Serves as a clinical role model, bringing scientific rigor and creative thinking to hematology clinical research</p></li></ul><p><br><strong>This role requires:</strong></p><ul><li><p>MD or equivalent required; MD/PhD strongly preferred, with fellowship training in Hematology or Oncology preferred</p></li><li><p>6-8 years of industry experience in related therapeutic area clinical development; cell therapy drug development experience preferred</p></li><li><p>Demonstrated track record across leadership roles, including work with senior clinical development staff and established credibility with external collaborators such as opinion leaders and regulators</p></li><li><p>Substantial drug development experience, including both IND and BLA/NDA submissions</p></li><li><p>Experience leading study start-up and execution, including data cleaning, medical review, database locks, and health authority responses</p></li><li><p>People management experience is a plus</p></li></ul><p><br>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Business Operations]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49982]]></requisitionid>
    <referencenumber><![CDATA[R49982]]></referencenumber>
    <apijobid><![CDATA[r49982]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49982/associate-manager-business-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Manager, Business Operations supports the development and execution of Business Operations functions, including data analysis, metrics reporting, process documentation, and project coordination. Under the guidance of senior team members, this individual contributes to operational initiatives, assists with vendor management activities, and helps drive efficiency improvements across the Global Development portfolio. This role is designed for emerging professionals who bring analytical rigor, collaborative energy, and a desire to grow within the pharmaceutical development operations environment.</p><br><h3>When & where:</h3><ul><li>Location: onsite in either Armonk, NY or Tarrytown, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Assist in collecting, organizing, and analyzing operational and financial data to support metrics reporting and performance tracking.</li><li>Support the development and maintenance of dashboards, scorecards, and reporting tools that monitor key Business Operations performance indicators.</li><li>Contribute to process documentation efforts, including drafting standard operating procedures, process maps, and training materials.</li><li>Coordinate meeting logistics, prepare agendas, capture minutes, and track action items for internal and cross-functional team meetings.</li><li>Assist with vendor management activities, including data collection, invoice tracking, and basic performance monitoring.</li><li>Support resource planning efforts by compiling headcount and capacity data for review by senior team members.</li><li>Participate in continuous improvement projects, contributing analysis and project coordination support.</li><li>Assist in managing select internal systems and tracking tools to ensure timely and accurate updates.</li><li>Engage with cross-functional stakeholders to gather inputs needed for reporting and operational projects.</li><li>Proactively identify data gaps or process inefficiencies and bring observations to manager for review.</li></ul><br><h3>This role requires:</h3><ul><li>Master of Business Administration (MBA) required, or MBA expected within 12 months of hire</li><li>Bachelor's Degree in a relevant field required Minimum of 4 years of industry experience required (pharmaceutical, biotech, CRO, consulting, or related field). Experience in clinical operations, business analytics, or project coordination preferred</li><li>Strong analytical and quantitative skills with comfort working with data sets</li><li>Proficiency in Microsoft Excel, PowerPoint, and Word; familiarity with data visualization tools a plus</li><li>Strong written and verbal communication skills</li><li>Detail-oriented with solid organizational skills and ability to manage multiple tasks</li><li>Collaborative team player who can work across functions</li><li>Proactive mindset and ability to work under guidance to meet deadlines</li><li>Demonstrated interest in pharmaceutical, biotech, or clinical operations</li><li>Intellectual curiosity and a continuous improvement orientation</li><li>Ability to handle confidential information with discretion</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 15:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Neuroscience / Genetic Medicine]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50139]]></requisitionid>
    <referencenumber><![CDATA[R50139]]></referencenumber>
    <apijobid><![CDATA[r50139]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50139/principal-scientist-neuroscience-genetic-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Scientist to join our Genetic Medicines team, helping advance the preclinical development of targeted genetic medicines for disorders of the central nervous system. In this role, you will design and lead experiments across CNS disease models, working as part of a collaborative, multidisciplinary team spanning platform technology, disease biology, and early clinical development.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Design experiments to evaluate the efficacy, target engagement, and delivery efficiency of viral and non-viral therapeutic candidates across CNS disease models</li><li>Design AAV transgene cassettes to optimize therapeutic efficacy</li><li>Lead a team of associates in the execution of experiments and analysis of primary data</li><li>Interpret complex datasets, integrating findings with current scientific literature to propose data-driven next steps</li><li>Communicate project strategy, scientific vision, and data updates to senior leaders</li><li>Author and review preclinical study reports to support regulatory submissions</li><li>Approach scientific problems with an engineering mindset and a design-build-test-learn framework</li><li>Coach and mentor junior scientists within a multidisciplinary team environment</li></ul><p><strong>This role requires:</strong></p><ul><li>Experience evaluating DNA- or RNA-based therapeutics in small-animal models</li><li>Hands-on experience with molecular biology techniques</li><li>Experience mentoring and managing research associates</li><li>Excellent communication and presentation skills</li><li>Preferred: Ph.D. in neuroscience, gene therapy, or a related discipline</li><li>Preferred: 5+ years of combined postdoctoral and industry experience in biotechnology, genetic medicines, or CNS drug discovery</li><li>Preferred: knowledge of both viral and non-viral genetic medicine delivery modalities</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Triage and Medical Review]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47768]]></requisitionid>
    <referencenumber><![CDATA[R47768]]></referencenumber>
    <apijobid><![CDATA[r47768]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47768/associate-director-triage-and-medical-review/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Global Patient Safety POD, supporting our global programmes in a hybrid role. In this role, you will lead end-to-end ICSR triage and medical review while collaborating with global safety and clinical development teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (Hybrid - three days a week on site)<br> </p><p><strong>Discover your role:</strong></p><ul><li><p>Oversee Individual Case Safety Report medical review and accurate data capture in Argus.</p></li><li><p>Lead triage harmonisation and end-to-end case quality across the India POD.</p></li><li><p>Review narratives, author analyses, causality rationale, and reporting decisions.</p></li><li><p>Guide expectedness determinations against programmes, products, and approved labelling.</p></li><li><p>Oversee clinically appropriate MedDRA coding for adverse events and medical history.</p></li><li><p>Partner with pharmacovigilance, risk management, and clinical teams before regulatory submissions.</p></li><li><p>Support compounds, case issue resolution, SOP development, process improvements, and inspection readiness.</p></li><li><p>You explore artificial intelligence technologies to strengthen pharmacovigilance activities.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MD or MBBS with active Indian registration or eligibility.</p></li><li><p>10+ years’ industry experience, including 7+ years in pharmacovigilance.</p></li><li><p>Hands-on ICSR review, narrative authoring, causality assessment, expectedness determination, and MedDRA coding.</p></li><li><p>Expert knowledge of ICH E2A, E2B, E2D, and FDA/EMA pharmacovigilance regulations.</p></li><li><p>Proficiency with Argus Safety or equivalent safety databases.</p></li><li><p>Strong clinical judgement and clear written rationale.</p></li><li><p>Global development or marketed product experience preferred.</p></li><li><p>GPS POD or insourced pharmacovigilance experience is advantageous.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Quality Assurance, Medical Device (Sustaining)]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47283]]></requisitionid>
    <referencenumber><![CDATA[R47283]]></referencenumber>
    <apijobid><![CDATA[r47283]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47283/senior-manager-quality-assurance-medical-device-sustaining/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our Medical Device QA team. This expanded leadership role will provide QA oversight across two critical functions: Combination Products Sustaining Engineering and Compliance. The position will lead a team of engineers and quality specialists.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Manage, mentor, and develop quality engineering and compliance teams</li><li>Standardize, streamline, and improve processes across sustaining and compliance</li><li>Implement digital, data-driven tools for accurate, consistent, and timely reporting</li><li>Lead teams through complex, ambiguous challenges in a pharmaceutical/medical device environment</li><li>Sustaining Engineering Support:<ul><li>Support sustaining engineering programs through risk assessment, design change management, and maintenance of the Design History File and Risk Management File</li><li>Advice and actively participate in Design Reviews associated with combination products</li><li>Provide QA and technical support to quality engineers and project teams during ongoing maintenance of the combination product</li><li>Interact with partners and contract organizations to ensure accurate completion of project milestones, including post-commercialization activities</li></ul></li></ul><ul><li>Combination Product Support:<ul><li>Act as Management Representative for the combination products QMS; own policies and procedures</li><li>Support regulatory inspections and partner audits for combination products</li><li>Keep the QMS current and inspection-ready via monitoring, gap assessments, and updates</li></ul></li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering and 8+ years of experience; including combination product or medical device experience; or equivalent combination of education & experience</li><li>Previous supervisory/ people leadership experience</li><li>Knowledge of the combination device development and lifecycle process</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Part_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior External Manufacturing Data Analyst]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50177]]></requisitionid>
    <referencenumber><![CDATA[R50177]]></referencenumber>
    <apijobid><![CDATA[r50177]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50177/senior-external-manufacturing-data-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill an External Manufacturing (EM) Data Analyst role to turn complex data into the insights that keep life-changing medicines moving efficiently from our manufacturing partners to the patients who need them. As part of our newly formed EM Center of Excellence, you’ll dig into real business problems, build the dashboards and analyses leadership relies on, and help shape how the EM network runs. This is a role for someone who thrives on turning ambiguity into clarity — and wants their work to matter.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work schedule: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Partner with business leaders and collaborators to gather requirements, document processes, and find opportunities for new business capabilities and process improvements</p></li><li><p>Develop and maintain dashboards and reports (e.g., Tableau, Power BI) that give leadership clear, real-time awareness of EM performance</p></li><li><p>Analyze capacity, performance, and other operational data to support Planning/Scheduling and drive EM strategy, process simplification, and standardization initiatives</p></li><li><p>Conduct root-cause and A3 problem-solving analysis, leading Continuous Improvement and Kaizen events (Process Mapping, Direct Observation, etc.) across the EM organization</p></li><li><p>Monitor and analyze metrics to identify gaps in current processes, improve service levels to internal and external customers, reduce waste, and improve value chain efficiency</p></li><li><p>Support implementation projects end-to-end, including requirements gathering, application and process design, testing, validation, and end-user knowledge transfer</p></li><li><p>Evaluate industry and market trends to identify new business solutions, and review opportunities to develop new products, technologies, and business models</p></li><li><p>Respond to ad hoc data analysis requests from across EM, and assist in developing presentations and EM strategy updates</p></li><li><p>Leverage AI to optimize processes and create efficiencies for workflows</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in business, data science, information technology, computer science, engineering, mathematics, statistics or related field, or equivalent combination of education and experience, for each level:</p></li><li><p>Specialist - 2+ years</p></li><li><p>Senior Specialist – 5+ years</p></li><li><p>Level will be determined based on experience</p></li><li><p>Previous experience in product management/project management/ and/or project leadership related activities is preferred</p></li><li><p>A natural problem solver who thrives in a fast-paced, high-pressure environment, prioritizing competing demands and hitting tight deadlines without sacrificing accuracy</p></li><li><p>Quickly learn new business processes and ask the right questions to close knowledge gaps, applying that understanding to guide your analysis</p></li><li><p>Translate ambiguous business questions into clear data requirements — knowing what data to pull, how to structure the analysis, and how to communicate the findings</p></li><li><p>Solid understanding of writing SQL to query relational databases; experience with programming languages such as Python is a plus</p></li><li><p>Expert in Excel and Business Intelligence tools (Tableau and Power BI); familiarity with IT project management tools is a plus</p></li><li><p>Strong situational analysis, decision-making, and process/operations improvement skills, with the ability to work independently against key timelines</p></li><li><p>Exceptional interpersonal and communication skills — written, verbal, and visual — with the confidence to present findings to senior leadership, influence decisions, and drive consensus across the organization</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 17:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director,  Program Operations Leader - Ophthalmology/Renal]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45092]]></requisitionid>
    <referencenumber><![CDATA[R45092]]></referencenumber>
    <apijobid><![CDATA[r45092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45092/director-program-operations-leader-ophthalmologyrenal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>For US Locations, this position is on-site 4 days per week and 1 day from home. A fully remote role is not possible for this position. </em></p><p>The Program Operations Leader (POL) is responsible for leadership of and setting and implementation of the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional strategy of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence.</p><p>In a typical day, you will:</p><ul><li>Be responsible for the overall success of the clinical study team(s) within a program(s)</li><li>Maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested</li><li>Provide operational insight into feasibility, timeline and cost estimates during clinical program/study development</li><li>Oversee clinical study timelines within a clinical program(s)</li><li>Provide input and operational insight into Clinical Study Concepts (CSC)</li><li>Be responsible for development and implementation of operational strategy, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol </li><li>Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency within the program and development of best practices within CTM</li><li>Oversee clinical study budgets within a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate</li><li>Ensure timely delivery of quality operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams within the clinical program(s). </li><li>Drive decision making and integrates all operational considerations for studies within a clinical program(s) to ensure goals are attainable prior to implementation</li><li>Act as point of contact for clinical program and study level escalation</li><li>Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress</li><li>Provide proactive creation and implementation of risk mitigation strategies</li><li>Provide innovative and flexible operational solutions and options to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges</li><li>Drives the strategy and oversight for vendor selection and management within a clinical program(s)</li><li>Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts</li><li>May require up to 25% travel</li></ul><p>To be considered, you must possess a Bachelor's degree and a minimum of 12 years of related in-house sponsor-side pharmaceutical experience, with 8 years in clinical operations.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Change Communications]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45838]]></requisitionid>
    <referencenumber><![CDATA[R45838]]></referencenumber>
    <apijobid><![CDATA[r45838]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45838/manager-internal-change-communications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an internal communications pro at the Manager level to help develop and drive communications targeting our 15,000+ colleagues globally. The successful candidate will join a dynamic and high-performing Internal Communications team that thinks strategically and executes at a high level to support our fast-growing company -- where colleagues are passionate about their work and our mission to bring important new medicines to patients in need. Internal Communications is part of the Corporate Affairs organization, which is focused on strengthening Regeneron’s reputation by developing strategies and programs that (1) distinguish our science, medicines and patient focus, (2) sustain culture and drive employee engagement, and (3) advance and differentiate our corporate responsibility commitments.</p><p><em><strong>This role will require 4 days per week onsite at our Global HQ Campus in Westchester, NY. This is not available as a fully remote / hybrid work.</strong></em></p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li><p>Support the development and execution of global communications programs that advance the goals of our key corporate functions (HR, IT, etc.) that are advancing critical innovation and digital transformation programs across the company.</p></li><li><p>Serve as trusted internal communications partner to leaders within G&A functions, advising on communications approaches that support enterprise priorities and initiatives.</p></li><li><p>Plan and coordinate key internal communications initiatives, demonstrating project management know-how and creative approaches that effectively inform, inspire and engage employees.</p></li><li><p>Draft compelling messaging – including project briefs, key messages, talking points, FAQ and other materials – that connect to company goals and priorities.</p></li><li><p>Develop informative and creative ways to communicate and engage employees about critical enterprise change initiatives, including digital transformation, global expansion, culture storytelling, and more.</p></li><li><p>Build strong relationships with colleagues at all levels of the organization to support collaboration.</p></li><li><p>Measure the effectiveness of communications and translate insights into actionable recommendations to improve reach, clarity and impact. </p></li><li><p>Identify and implement opportunities to elevate the strategic focus of communications, streamline processes, and improve overall efficiency and effectiveness.</p></li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li><p>Experienced in planning and executing communications initiatives, including storytelling and content management, that engage a busy, global employee base.</p></li><li><p>Knowledge and understanding of change communication principles that help employees navigate organizational change and connect to the opportunity that change presents.</p></li></ul><ul><li><p>Outstanding verbal and written communication skills, with the ability to translate complex topics into clear, accessible messaging tailored to diverse audiences.</p></li><li><p>Knowledge of and experience with channels, approaches and technologies that are used to communicate and connect with employees (intranets, enterprise social platforms, email distribution tools, etc.)</p></li><li><p>Ability to manage and prioritize multiple tasks and projects, adapt quickly to changing priorities and needs, and meet deadlines in a fast-paced environment.</p></li><li><p>Exceptional project management skills, strong attention to detail, sound judgment and curiosity to learn.</p></li></ul><p><strong>To be considered you must have a:</strong></p><ul><li><p>Bachelor's degree</p></li><li><p>Minimum 4+ relevant experience in internal communications and employee engagement.</p></li></ul><ul><li><p>Previous employment in a PR/Communications agency and/or the pharma/biotech industry preferred but not required.</p></li><li><p>Experience in a communications role supporting corporate or business functions, including HR, IT, etc.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - GRAND RAPIDS, MI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48049]]></requisitionid>
    <referencenumber><![CDATA[R48049]]></referencenumber>
    <apijobid><![CDATA[r48049]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48049/medical-account-specialist-ii-neurology-grand-rapids-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Grand Rapids]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Grand Rapids (Metro), Michigan </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MINNEAPOLIS, MN]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48066]]></requisitionid>
    <referencenumber><![CDATA[R48066]]></referencenumber>
    <apijobid><![CDATA[r48066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48066/medical-account-specialist-ii-neurology-minneapolis-mn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minneapolis]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Minneapolis (Metro), Minnesota</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MILWAUKEE, WI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48054]]></requisitionid>
    <referencenumber><![CDATA[R48054]]></referencenumber>
    <apijobid><![CDATA[r48054]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48054/medical-account-specialist-ii-neurology-milwaukee-wi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milwaukee]]></city>
    <state><![CDATA[Wisconsin]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Milwaukee (Metro), Wisconsin</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LAS VEGAS, NV]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48077]]></requisitionid>
    <referencenumber><![CDATA[R48077]]></referencenumber>
    <apijobid><![CDATA[r48077]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48077/medical-account-specialist-ii-neurology-las-vegas-nv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Las Vegas]]></city>
    <state><![CDATA[Nevada]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Las Vegas (Metro), NV</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - NEW ORLEANS, LA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48058]]></requisitionid>
    <referencenumber><![CDATA[R48058]]></referencenumber>
    <apijobid><![CDATA[r48058]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48058/medical-account-specialist-ii-neurology-new-orleans-la/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New Orleans]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: New Orleans (Metro), LA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (Skin) - North East]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46312]]></requisitionid>
    <referencenumber><![CDATA[R46312]]></referencenumber>
    <apijobid><![CDATA[r46312]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46312/sales-specialist-oncology-skin-north-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is growing its newly established International Oncology organisation and is seeking a Sales Specialist to join the UK sales team. This role focuses on engaging oncology healthcare professionals, supporting effective clinical practice through high‑quality scientific exchange, and representing Regeneron Oncology across the local healthcare system. The position offers the opportunity to contribute to a developing oncology portfolio while working closely with cross‑functional colleagues.</p><h3><strong>When and where</strong></h3><ul><li><strong>Location & work model:</strong> UK‑based, field‑facing role</li><li><strong>Travel:</strong> Frequent travel required, including attendance at meetings and congresses</li></ul><h3><strong>Discover your role</strong></h3><ul><li>Engage oncology healthcare professionals through compliant, scientific discussions</li><li>Understand local healthcare environments and account context</li><li>Communicate agreed brand messages to support objectives</li><li>Develop and implement territory and account plans using data and insights</li><li>Manage key accounts in line with regional and country guidance</li><li>Work closely with medical colleagues on regional activities</li><li>Represent Regeneron Oncology at national and international meetings</li><li>Report performance and market insights to UK leadership</li></ul><h3><strong>This role requires</strong></h3><ul><li>Comfort managing a defined territory and multiple accounts</li><li>A planned and structured approach to customer engagement</li><li>Flexibility to adapt activity based on account and market needs</li><li>Confidence using face‑to‑face, remote, and digital engagement channels</li><li>Consistent adherence to industry codes and company procedures</li><li>Professional conduct grounded in integrity and ethics</li></ul><h3><strong>Required qualifications</strong></h3><p>A Bachelor’s degree, or recognised equivalent for sales professionals, is required. The role requires experience in customer engagement and disease‑ or concept‑led selling, with the ability to present effectively to varied audiences. Strong planning and prioritisation capability and competence using CRM systems and multiple IT platforms are essential. Qualification in the relevant pharmaceutical industry Code of Practice (such as ABPI or EFPIA), fluency in English, and willingness to travel frequently are required.</p><p><strong>Preferred:</strong> Experience within the biotech or pharmaceutical sector, oncology sales exposure, and launch experience.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Statistical Programming - Pharmacometrics]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47328]]></requisitionid>
    <referencenumber><![CDATA[R47328]]></referencenumber>
    <apijobid><![CDATA[r47328]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47328/associate-director-statistical-programming-pharmacometrics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director Pharmacometrics Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. Provides project leadership, resource planning/coordinating deliverables within project or across multiple projects. Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement and programming specifications using internal standards and guidelines. Providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. The incumbent is responsible for addressing administrative functions required for project management such as compilation of resource requirements and milestones, identifying/communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies.</p><p><strong><em>This position requires 4 days onsite presence based out of our Tarrytown, NY or Warren, NJ location.</em></strong></p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Lead the programming and QC of analysis datasets, TFL's across multiple projects or standard tools following Regeneron standard data models or user requirements. Representation of PMX programming functions and coordination of activities with cross line functions and support planning/coordinating timelines in data exchange, deliverables. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.</p></li><li><p>Lead the integration of data across studies in support of Exposure-response, PopPK and PopPKPD analysis and 2.7.2.</p></li><li><p>Provide programming support for all PMX deliverable in HAR request, data driven analysis, publications, conference</p></li><li><p>Plan and lead the creation and validation of electronic submission requirements (i.e. annotated CRF, data export files, define documents).</p></li><li><p>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Expert SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment</p></li><li><p>Understanding of relational database structure and reporting systems utilizing multiple data delivery applications</p></li><li><p>Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards.</p></li><li><p>Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis), experienced in data handling, process and analysis and able to understand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner</p></li><li><p>Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.</p></li><li><p>Good Skilled in use of relevant software, including Window SAS, SAS studio (Base, Stat, Macro, graph), MS-Excel, R programming and/or Python.</p></li><li><p>Good knowledges in AI use case in statistical programming and data sciences.</p></li></ul><p><strong>To be considered for this opportunity</strong> you must have a Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline. 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. Experience in project and people management, and expertise in one or more therapeutic areas is also preferred. SAS Certification desirable in statistics, computer science.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Data Reporting]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47785]]></requisitionid>
    <referencenumber><![CDATA[R47785]]></referencenumber>
    <apijobid><![CDATA[r47785]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47785/manager-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><p>As a Manager, Clinical Data Management Reporting, you will lead the development and delivery of high-quality clinical data reporting solutions that support efficient data review, operational oversight, and decision-making across clinical development programs. You will play a key role in transforming complex clinical and operational data into clear, actionable insights while ensuring consistency, accuracy, and compliance.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Leading the design, development, and maintenance of standardized clinical data reports and listings to support data review and clinical trial oversight</p></li><li><p>Partnering with cross-functional teams to gather reporting requirements and translate them into high-quality, accurate, and timely outputs</p></li><li><p>Delivering participant-level listings, exception reports, and reconciliation outputs to enable efficient data cleaning and review</p></li><li><p>Driving reporting solutions that provide actionable insights for operational performance and decision-making</p></li><li><p>Collaborating with data management and technology teams to leverage EDC systems, data lakes, and external data sources</p></li><li><p>Providing subject matter expertise in clinical data reporting, data structures, and reporting workflows</p></li><li><p>Identifying opportunities for automation and process improvement to enhance reporting efficiency and scalability</p></li><li><p>Monitoring data flows and troubleshooting issues related to data accuracy, completeness, and refresh cycles</p></li><li><p>Supporting inspection readiness by ensuring reporting outputs are compliant, traceable, and audit-ready</p></li><li><p>Delivering insights to identify risks, bottlenecks, and opportunities for operational improvement</p></li><li><p>Ensuring compliance with regulatory requirements such as GCP, ICH, and data privacy standards</p></li><li><p>Supporting training initiatives and development of reporting frameworks, standards, and documentation</p></li><li><p>Providing guidance and mentorship to team members and contributing to team development</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Strong experience in clinical data management, reporting, and data visualization</p></li><li><p>Good understanding of clinical trial processes, data standards (CDISC), and regulatory requirements</p></li><li><p>Experience working with EDC systems such as Medidata Rave</p></li><li><p>Proficiency in reporting and visualization tools such as SAS, R, Tableau, Power BI, Spotfire, or similar</p></li><li><p>Experience with data integration, data lakes, data pipelines, and automation frameworks</p></li><li><p>Strong knowledge of data lifecycle management and risk-based data review concepts</p></li><li><p>Excellent problem-solving, communication, and stakeholder management skills</p></li></ul><div><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s or Master’s degree in Data Science, Computer Science, Life Sciences, or a related field</p></li><li><p>7+ years of experience in clinical data, reporting, or related domains</p></li><li><p>Strong hands-on experience in clinical data reporting, analytics, and visualization</p></li><li><p>Experience working in a regulated clinical or pharmaceutical environment</p></li></ul></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Finance Service Delivery Analyst]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47446]]></requisitionid>
    <referencenumber><![CDATA[R47446]]></referencenumber>
    <apijobid><![CDATA[r47446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47446/finance-service-delivery-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Finance Service Delivery Analyst to join our Financial Shared Services team, supporting our global payroll and accounting operations in a hybrid work model. In this role, you will support standardized financial processes, ensure accurate reporting, and drive efficiency across global operations while collaborating with international teams and stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Perform reconciliations between enterprise systems and external vendor systems to ensure data accuracy</p></li><li><p>Prepare and reconcile payroll data templates supporting processing across multiple global countries</p></li><li><p>Implement established payroll and accounting procedures consistently to support centralized operations</p></li><li><p>Coordinate and support month-end, quarter-end, and year-end close processes, including preparation of schedules impacting reporting</p></li><li><p>Assist in preparing reports, audit documentation, and materials for compliance reviews</p></li><li><p>Collaborate with international teams to deliver operational support and ensure seamless service delivery across regions</p></li><li><p>Maintain process documentation, mappings, and Standard Operating Procedures (SOPs) while ensuring adherence to governance practices and internal controls</p></li><li><p>You proactively identify and drive opportunities to improve efficiency and consistency within financial operations.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in Accounting, Finance, Business, Data Analytics, or related field (B.Com or BBM preferred)</p></li><li><p>Minimum 2+ years of experience in payroll, accounting, or data analysis</p></li><li><p>Experience performing reconciliations between enterprise systems and external vendor systems</p></li><li><p>Experience preparing and reconciling payroll data templates across multiple global countries</p></li><li><p>Knowledge of accounting month-end close processes and financial reporting schedules</p></li><li><p>Experience supporting audit preparation and compliance documentation</p></li><li><p>Understanding of governance practices, internal controls, and regulatory compliance requirements</p></li><li><p>Strong customer service and stakeholder communication skills when addressing associate inquiries</p></li><li><p>Ability to collaborate effectively with international, cross-regional teams</p></li><li><p>Proactive approach to identifying process improvements and driving operational efficiencies</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48310]]></requisitionid>
    <referencenumber><![CDATA[R48310]]></referencenumber>
    <apijobid><![CDATA[r48310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48310/senior-specialist-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist, External Data Acquisition and Delivery to join our Clinical Data Management team in a hybrid role. In this role, you will manage end-to-end non-Case Report Form data across assigned studies or Clinical Development Units - developing or amending Data Transfer Specifications of low to medium complexity with minimal supervision, performing external data reconciliation and ensuring vendor data is accurately transferred and cleaned in accordance with study protocols and Data Management Plan - while collaborating with external data vendors, CRO partners and cross-functional stakeholders. Ensure compliance with Regeneron SOPs, regulatory requirements, and industry best practices. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Develop Data Transfer Specifications (DTS) for assigned studies or Clinical Development Units as per study timelines.</li><li>Author and maintain DTS documents using standard templates and CDISC requirements, in collaboration with internal and external stakeholders.</li><li>Act as the primary technical point of contact between clinical data management and vendors.</li><li>Respond to vendor and stakeholder queries to ensure external data is complete, correctly structured and delivered in the required format.</li><li>Track DTS status, milestones and deliverables across data types and programs, escalating issues and following through to resolution.</li><li>Process change requests, support data structure issue resolution and facilitate the creation of new test codes where required.</li><li>Reconcile external vendor data against clinical database to ensure accurate transfer, completeness and consistency across all data sources.</li><li>Support data locking, archival, reconciliation documentation, eTMF maintenance and ensure inspection readiness standards.</li><li> Provide review of protocol requirements, vendor specifications, and operational data flows with minimal supervision.</li><li>You guide CROs, vendors and cross-functional partners with clear technical direction while identifying areas for process improvement.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Science, Health, Mathematics, Engineering, Computational or related field.</li><li>4+ years in external clinical data acquisition or management within biotechnology, pharmaceutical or a health-related industry.</li><li>Experience managing multiple clinical data types and formats such as biomarker, eCOA, imaging, ECG, PK, genomics and laboratory data.</li><li>Knowledge of 21 CFR Part 11, ICH-GCP guidelines and CDISC standards for data collection.</li><li>Proficiency extracting data into SAS, CSV and XML formats.</li><li>Experience with EDC platforms such as Medidata Rave, Veeva or Oracle Inform, and external data reconciliation and query processes between EDC and vendor systems.</li><li>Basic knowledge of database structures and protocol review as relevant to clinical data management is preferred.</li><li> Ability to draw from wide-ranging experience to resolve complex issues.</li><li> Strategic thinking, creativity, and problem-solving skills essential</li><li> Ability to work effectively with and motivate virtual teams in a matrix environment.</li><li>Good interpersonal, oral, and written communication skills.</li><li>Society of Clinical Data Management certification is recommended.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Tax]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48870]]></requisitionid>
    <referencenumber><![CDATA[R48870]]></referencenumber>
    <apijobid><![CDATA[r48870]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48870/manager-tax/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager Tax Compliance and Indirect Tax Operations India to join our Finance and Tax function, supporting our global tax operations in a hybrid work model. In this role, you will lead tax compliance and reporting activities across global value-added tax (VAT) and income tax processes while collaborating with finance, information technology, supply chain, procurement, operations teams, and external advisors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Support global VAT and international tax compliance through preparation, review, and filing activities delivered with external co-source partners.</p></li><li><p>Lead end-to-end VAT reconciliations, validate transactional data, investigate variances, and prepare audit-ready reporting files.</p></li><li><p>Maintain VAT ledgers by reconciling VAT accounts across returns, balance sheet, income statement, e-reporting, and Intrastat filings.</p></li><li><p>Monitor changes in global VAT legislation and assess the impact on business operations and compliance requirements.</p></li><li><p>Coordinate responses to VAT and income tax queries, provide practical guidance, and document tax positions through technical memos.</p></li><li><p>Ensure timely and accurate income tax calculations and reporting for statutory financial statements and corporate reporting obligations.</p></li><li><p>Support tax audits, inquiries, and regulatory notices by providing accurate documentation and responses.</p></li><li><p>Build strong cross-functional partnerships, mentor junior tax professionals, and foster a collaborative, process-driven tax function.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in Accounting, Finance, Taxation, or a related field.</p></li><li><p>CA, CPA, EA, or equivalent professional certification preferred.</p></li><li><p>7–9+ years of experience in tax compliance and tax operations.</p></li><li><p>Strong knowledge of global direct and indirect tax, including in-depth understanding of VAT legislation and statutory requirements.</p></li><li><p>Experience preparing and overseeing income tax reporting aligned with local statutory and corporate requirements.</p></li><li><p>Knowledge of cross-border transactions and related tax implications.</p></li><li><p>Experience working in multinational or global tax environments preferred.</p></li><li><p>Exposure to enterprise resource planning systems such as Oracle and tax reporting tools is desirable.</p></li><li><p>Strong analytical and problem-solving skills, with experience using artificial intelligence or automation technologies considered a plus.</p></li><li><p>Experience managing and developing teams.</p></li><li><p>Excellent communication and interpersonal skills, with the ability to engage effectively with diverse partners.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology – Washington DC / Baltimore]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48562]]></requisitionid>
    <referencenumber><![CDATA[R48562]]></referencenumber>
    <apijobid><![CDATA[r48562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48562/medical-specialist-ii-ophthalmology-washington-dc-baltimore/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Territory: Washington DC / Baltimore</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets several medicines, including for eye diseases, and has product candidates in development in other areas of high unmet medical need.</p><p><strong>A typical day might include the following:</strong><br>The Medical Specialist II will report to the Regional Director and will be responsible for daily development and management of relationships with Retina Specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The primary focus on this role will be the approved indications suffered by patients as it relates to conditions of the eye. The Medical Specialist II will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you:</strong><br>• Have experience in biologics and buy and bill products<br>• Can demonstrate history of high sales performance<br>• Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Ophthalmology and/or Buy & Bill with relevant retina experience is preferred. Residency in the territory is required and occasional overnights expected.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Central Monitoring]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47804]]></requisitionid>
    <referencenumber><![CDATA[R47804]]></referencenumber>
    <apijobid><![CDATA[r47804]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47804/manager-central-monitoring/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Central Monitoring, Data Analysis to join our Global Clinical Trial Services team. In this role, you will oversee centralized monitoring activities for global and complex clinical trials and support the configuration, execution, and maintenance of Risk-Based Quality Management (RBQM) platforms. You will leverage your programming and analytical expertise to create customized analyses, automate workflows, integrate data systems, and deliver actionable insights that support informed decision-making and optimize clinical trial performance. You may also oversee multiple studies within an assigned therapeutic area, lead process-improvement initiatives, and collaborate with cross-functional teams and industry partners to advance central monitoring capabilities.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Act as a subject-matter expert for the configuration, implementation, and execution of Central Monitoring RBQM platforms across studies.</p></li><li><p>Maintain Regeneron Central Monitoring Key Risk Indicator and Quality Tolerance Limit libraries to ensure consistent deployment across studies and alignment with regulatory requirements.</p></li><li><p>Configure studies within an RBQM platform by partnering with functional and cross-functional stakeholders to develop Central Monitoring configuration specifications.</p></li><li><p>Provide operational expertise, training, and guidance, serving as an escalation point for issues related to the Central Monitoring RBQM platform.</p></li><li><p>Conduct central monitoring reviews as required, including recurring data refreshes and troubleshooting execution errors in support of Study Central Monitors.</p></li><li><p>Apply programming expertise to support Central Monitoring data analysis, automation, reporting, and system integration.</p></li><li><p>Interpret and present Key Risk Indicator and Key Performance Indicator data to support informed decision-making.</p></li><li><p>Contribute to the continuous improvement and standardization of technologies, systems, processes, and training materials that support Central Monitoring and RBQM.</p></li><li><p>Represent Central Monitoring in process-improvement initiatives and collaborate effectively with internal and external stakeholders.</p></li><li><p>Oversee multiple studies within an assigned therapeutic area, as applicable, and contribute to innovation in central monitoring capabilities.</p></li><li><p>Travel up to 25%, as required.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>At least 7 years of relevant biotechnology or pharmaceutical industry experience. Experience in Central Monitoring, site monitoring, or data management is preferred.</p></li><li><p>A minimum of 2 years of direct experience with RBQM systems.</p></li><li><p>Technical expertise in database design, system configuration, and report development, with experience managing RBQM or similar platforms.</p></li><li><p>Proficiency in programming languages such as Python, R, SQL, or SAS, with the ability to develop scripts for data analysis, automation, and system integration.</p></li><li><p>Strong analytical, critical-thinking, and problem-solving skills, including experience troubleshooting data refreshes and resolving execution errors in analytical systems.</p></li><li><p>Working knowledge of the clinical drug-development process, including ICH and GCP guidelines and applicable regulatory requirements.</p></li><li><p>Experience with clinical databases, electronic data-capture systems, quality-control processes, and auditing procedures.</p></li><li><p>The skills for mathematical concepts, statistical methodologies, and data analytics, with the ability to interpret KRIs and KPIs.</p></li><li><p>The ability to identify and interpret current and emerging business trends and apply them to centralized monitoring practices.</p></li><li><p>Effective interpersonal, verbal, and written communication skills, with the ability to convey sophisticated technical and analytical insights clearly and concisely.</p></li><li><p>The ability to collaborate across cross-functional teams and build effective internal and external relationships.</p></li><li><p>Proficiency in Microsoft Office applications, including sophisticated Excel skills for data manipulation and reporting.</p></li><li><p>Experience using CluePoints or a similar centralized monitoring and risk-based quality management solution is preferred</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Purification Development (PMPD)]]></title>
    <date><![CDATA[Mon, 20 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48581]]></requisitionid>
    <referencenumber><![CDATA[R48581]]></referencenumber>
    <apijobid><![CDATA[r48581]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48581/process-development-engineer-iii-purification-development-pmpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer III</strong> to join our Preclinical Manufacturing & Process Development (PMPD) group, on-site in Tarrytown, NY. In this exciting role, you will use your domain expertise in liquid chromatography separations to design, lead, and react to experiments and projects independently, while mentoring less experienced direct reports and team members within the Purification Development (PD) group.</p><p>This position offers the opportunity to act as an established authority in chromatography-based separation techniques, proactively identifying improvement opportunities and driving strategy across Regeneron in support of pipeline and assay development, and the release of clinical and commercial products.</p><p><strong>When & where:</strong></p><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site in Tarrytown, NY</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to maintain lab operations and support equipment</li></ul><p><strong>What you'll do:</strong></p><ul><li>Act as an established authority in chromatography-based separation techniques, demonstrating scientific acumen across Regeneron, and determine strategies for improvements</li><li>Begin to lead technology development independently, drive results, and onboard new technologies</li><li>Skillfully write and review complex technical documents typically reviewed by senior leadership</li><li>Take calculated risks to achieve goals, independently and accurately determining strategies to address gaps and implement them effectively</li><li>Ask pointed questions to eliminate ambiguity and provide appropriate solutions</li><li>Make science-based recommendations through novel incorporation of internal and external (literature) learnings</li><li>Maintain and continuously improve lab operations and relevant data or knowledge management systems within your area of expertise</li><li>Anticipate customer needs at an organizational level and proactively shape internal workflows to meet them</li><li>Prepare and deliver effective oral presentations in internal and external professional meetings, sharing cross-functional skills and knowledge</li><li>Collaborate across Regeneron and external groups, with regular interaction with PMPD Senior Leadership</li><li>Represent PMPD in external multi-functional meetings</li><li>Mentor peers, direct reports, and PMPD personnel directly or indirectly through leading, guiding, and assisting</li><li>Contribute to lab equipment maintenance and safety, anticipating and resolving potential problems with supplies and equipment</li><li>Keep up with SOP training and compliance responsibilities</li><li>Communicate relevant information to PMPD Senior Staff as departmental program team representative</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>This is an on-site laboratory role requiring hands-on use of specialized equipment, including Akta Explorer/Avant, Akta Pilot, BioProcess Skid, disc stack centrifuge, depth and tangential/normal flow filtration systems, chromatographic columns, HPLC, UPLC, diafiltration skid, and Raman spectroscopy, as well as laminar flow hoods and chemical fume hoods.</li><li>Flexibility to multi-task, work both independently and within a team environment, and take calculated risks to solve complex, ambiguous problems is required.</li></ul><p><strong>Let's find out if we're a fit:</strong></p><p>Must-haves:</p><ul><li>Degree in an engineering discipline, with 0-2+ years of experience (PhD), 3-5+ years (MS), or 7-10+ years (BS) of industrial experience</li><li>Industrial experience in protein purification</li><li>Demonstrated ability to communicate complex messages clearly and credibly with multifaceted audiences, establishing multi-functional relationships that support proactive teamwork across the organization</li><li>Experience with specialized laboratory software and systems, including Empower, Unicorn, PI Historian, JMP, LIMS, Spotfire, RPES, and ELN</li></ul><p>Preferred / nice-to-haves:</p><ul><li>Demonstrated innovative thinking, developing ideas, tools, or techniques to solve problems or improve established procedures</li><li>Experience leading a team and effectively delegating tasks</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42183]]></requisitionid>
    <referencenumber><![CDATA[R42183]]></referencenumber>
    <apijobid><![CDATA[r42183]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42183/associate-director-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Clinical Data Management</strong> team.</p><p>As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron’s clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio</p></li><li><p>Serving as a portfolio-level lead for external data quality and clinical-data operational strategy</p></li><li><p>Reviewing protocol requirements, vendor specifications, and operational data flows</p></li><li><p>Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines</p></li><li><p>Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data</p></li><li><p>Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring</p></li><li><p>Establishing and handling vendor KPIs, SLAs, and quality metrics</p></li><li><p>Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency</p></li><li><p>Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies</p></li><li><p>Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies</p></li><li><p>Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions</p></li><li><p>Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management</p></li><li><p>Supporting SOP development, inspection readiness, audit activities, and regulatory compliance</p></li><li><p>Representing EDAD in leadership forums, governance committees, and technology discussions</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10+ years of experience in Clinical Data Acquisition/Management within biotechnology, pharmaceutical, or healthcare industries</p></li><li><p>Minimum 4+ years of people management experience</p></li><li><p>Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms</p></li><li><p>Experience driving process improvements and vendor oversight in supervised environments</p></li><li><p>Bachelor’s degree in Science, Health, Mathematics, Computing, Information Systems, or a related field</p></li><li><p>Advanced degree preferred</p></li><li><p>Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data</p></li><li><p>Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform</p></li><li><p>Experience working with SAS, CSV, and XML data formats</p></li><li><p>Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Proven experience handling external vendor relationships and driving accountability for quality deliverables</p></li><li><p>Strong leadership, people management, coaching, and mentoring capabilities</p></li><li><p>Strategic thinking, creativity, problem-solving, and analytical skills</p></li><li><p>Strong project management and stakeholder management capabilities</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Ability to work effectively in a fast-paced, matrixed, and global environment</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst - Therapeutic Focus Areas]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48892]]></requisitionid>
    <referencenumber><![CDATA[R48892]]></referencenumber>
    <apijobid><![CDATA[r48892]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48892/principal-business-analyst-therapeutic-focus-areas/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Principal Business Analyst Therapeutic Focus Areas, will work collaboratively with Research & Preclinical Development scientists, as well as other IT stakeholders, to understand and document scientific lab and data processes, and translate these into requirements for the development of data and technology solutions that support Regeneron’s scientific mission.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Translate business strategies, goals, and objectives into clear requirements; document problem statements with quantifiable business value</p></li><li><p>Document “as is” and “to be” business processes; identify, verify, and document functional and non-functional requirements using standard methodologies and tools</p></li><li><p>Map information system connections and data flows between systems; identify data elements and provide data mapping and data dictionaries</p></li><li><p>Write SQL statements to investigate data; understand data lake principles and different database types</p></li><li><p>Maintain and prioritize the backlog of requests; ensure the development team has absolute clarity on requirements; manage business stakeholder expectations</p></li><li><p>Work with scientists and laboratory personnel to understand business processes and suggest improvements; partner with research scientists and technical teams to define system goals and requirements</p></li><li><p>Pursue data quality issues to root cause; collaborate with business and IT partners to address issues intelligently</p></li><li><p>Handle a variety of tasks, effectively solve problems with complex variables, and shift priorities as needed in a fast-paced research environment</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Master’s degree in a life science with experience in computer science or information technology.</p></li><li><p>5+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment.</p></li><li><p>Previous experience in the biotechnology and/or pharmaceutical industry is required. We need someone who is adept at using a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, data modeling frameworks) in order to perform business analysis, elicit and document requirements, map data flows, and drive data quality improvements in a research-focused environment. </p></li><li><p>Previous experience with biological laboratory techniques, bioinformatics methods, relational database concepts, IT project and software development lifecycle methodologies, and managing or leading software development projects is preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - RALEIGH, NC]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48925]]></requisitionid>
    <referencenumber><![CDATA[R48925]]></referencenumber>
    <apijobid><![CDATA[r48925]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48925/medical-account-specialist-ii-hematology-raleigh-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Raleigh, NC</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Associate Scientist, Metabolic & Muscle Diseases]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48549]]></requisitionid>
    <referencenumber><![CDATA[R48549]]></referencenumber>
    <apijobid><![CDATA[r48549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48549/sr-associate-scientist-metabolic-muscle-diseases/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Associate Scientist to join our Obesity, Metabolism and Muscle Diseases Group, serving as a central histological resource providing expert tissue processing and staining services across multiple research programs simultaneously. In this role, you will manage end-to-end histological workflows spanning a broad range of tissue types, maintaining rigorous quality standards while navigating competing program demands to deliver high-quality data on time.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Process tissue samples from multiple tissue types (e.g., liver, heart, brain, muscle, adipose), including fixation, dehydration, clearing, embedding, and sectioning</p></li><li><p>Perform routine and special histological staining according to program needs</p></li><li><p>Conduct IHC and IF, developing, optimizing, and validating new protocols, antibody titrations, and antigen retrieval conditions</p></li><li><p>Apply in situ hybridization (ISH/RNAscope) techniques for gene expression localization where required</p></li><li><p>Perform image acquisition using various scanning platforms and manage image data repositories</p></li><li><p>Perform quantitative image analysis, developing and applying customized algorithms as needed</p></li><li><p>Generate high-quality figures and data summaries for internal reports, regulatory packages, and peer-reviewed publications</p></li><li><p>Maintain and communicate a dynamic workload tracker, proactively flagging capacity constraints or scheduling conflicts to stakeholders</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS with 5+ years or MS with 2+ years of relevant experience</p></li><li><p>Proficiency in standard and special histochemical staining techniques across multiple tissue types</p></li><li><p>Demonstrated IHC/IF assay development, optimization, and troubleshooting experience</p></li><li><p>Proficiency with whole-slide imaging systems and digital pathology image analysis software (e.g., HALO)</p></li><li><p>Strong organizational and record-keeping skills, with the ability to manage and prioritize simultaneous requests from multiple stakeholders</p></li><li><p>Excellent oral and written communication skills</p></li><li><p>Preferred: experience with in situ hybridization platforms (RNAscope, BaseScope, FISH)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Senior Scientist – Autoimmunity, Immunology and Inflammation]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48713]]></requisitionid>
    <referencenumber><![CDATA[R48713]]></referencenumber>
    <apijobid><![CDATA[r48713]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48713/sr-senior-scientist-autoimmunity-immunology-and-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Scientist to join our Immunology and Inflammation team, leading innovative research programs that connect deep mechanistic biology with therapeutic discovery. In this role, you will shape experimental strategy, design rigorous in vitro and in vivo studies, and interrogate novel immune pathways, while collaborating with talented scientists across disciplines to advance high-impact programs in Regeneron's pipeline.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead complex in vivo studies in mouse models of inflammatory disease to evaluate therapeutic efficacy and define mechanism of action</p></li><li><p>Build and optimize primary cell-based assays and high-content immunological readouts, including multi-parameter flow cytometry, ELISA/MSD, and histology</p></li><li><p>Interrogate cytokine and immunoreceptor pathways to generate decision-enabling data</p></li><li><p>Influence project direction by interpreting complex datasets and communicating clear scientific recommendations to project teams, leadership, and external collaborators</p></li><li><p>Mentor junior scientists and research associates, contributing to an inclusive, collaborative culture</p></li><li><p>Shape research questions and troubleshoot complex programs from concept through readout as an independent, hypothesis-driven scientist</p></li><li><p>Partner across disciplines to move discovery programs forward, energized by cross-functional collaboration</p></li><li><p>Stay intellectually curious and adaptable, learning new approaches as scientific questions and priorities evolve.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D.+ 0-4 years in Immunology, Biology, Cellular and Molecular Biology, or a related discipline, or MS with at least 8 years of relevant industry or academic research experience</p></li><li><p>Hands-on expertise with mouse models of inflammatory diseases</p></li><li><p>Experience with multi-parameter flow cytometry, primary cell culture and cell-based assays, ELISA/MSD, and standard molecular techniques</p></li><li><p>Strong peer-reviewed publication record and demonstrated ability to lead independent research programs</p></li><li><p>Deep immunology expertise and strong analytical thinking, with the ability to translate complex data into clear scientific conclusions</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Developer - Automation Core]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48957]]></requisitionid>
    <referencenumber><![CDATA[R48957]]></referencenumber>
    <apijobid><![CDATA[r48957]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48957/sr-developer-automation-core/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking an outstanding Sr. Developer to design, develop, and deliver informatics solutions that enable our research and preclinical development pipeline. This role focuses on LIMS/ELN platform development, scientific data integrations, and building AI-powered capabilities that accelerate scientific workflows. The ideal candidate brings a data-first perspective, approaching every problem by understanding the underlying data, its structure, and how it flows across systems before writing code. You will serve as a technical lead driving architecture decisions and delivering high-quality solutions on COTS platforms including Sapio, Benchling, and Dotmatics. The ideal candidate will collaborate across diverse scientific and engineering functions to achieve organizational goals.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>When: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li>Own the design and development of server-side plugins, integrations, and workflows on LIMS/ELN platforms (Sapio preferred) using Java and Python.</li><li>Architect and build AI/GenAI-enabled solutions (LLM agents, RAG pipelines, prompt-engineered workflows) to streamline R&pD informatics processes.</li><li>Develop data pipelines and integrations between scientific instruments, LIMS/ELN systems, and enterprise data platforms owning data modeling, transformation logic, and data quality validation end-to-end.</li><li>Serve as technical lead on projects, defining logical approach, and conducting code reviews.</li><li>Partner with scientists, lab operations, and product owners to translate scientific requirements into scalable technical solutions.</li><li>Design and implement digital solutions to streamline day-to-day lab operations, improve efficiency, and support data-driven workflows across Core laboratories.</li><li>Evaluate and implement COTS platform capabilities (Sapio, Benchling, Dotmatics) to enhance out-of-the-box functionality.</li><li>Design and develop REST APIs, webhooks, and middleware to enable interoperability across R&pD systems.</li><li>Apply a data-first approach to problem-solving; analyze scientific datasets, identify data quality issues, build dashboards and reporting solutions, and translate data insights into actionable recommendations for scientific collaborators.</li><li>Contribute to platform modernization initiatives, including cloud migration and containerized deployments.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor's degree in Computer Science, Bioinformatics, Life Sciences, or related field with 3+ years of work experience in software development supporting life sciences R&pD or laboratory informatics.</li><li>Proficiency in Java (server-side development, plugin architectures).</li><li>Proficiency in Python (scripting, data pipelines, webhooks, automation).</li><li>Experience with at least one LIMS or ELN platform: Sapio, Benchling, or Dotmatics. Experience with Sapio LIMS/ELN (server-side plugins, workflows, data model configuration) is preferred.</li><li>Proven experience with AI/GenAI technologies: building LLM-powered agents, prompt engineering, retrieval-augmented generation (RAG), or AI-assisted workflow automation. Experience with AI agent frameworks (LangChain, LlamaIndex, Claude/Anthropic APIs, OpenAI APIs) is preferred.</li><li>Experience with instrument integrations (TetraScience or direct instrument interfaces) is preferred.</li><li>Familiarity with lab automation integration scheduling platforms, such as HighRes Cellario, and the APIs used to connect scheduling software with instruments is preferred.</li><li>Experience creating custom drivers for laboratory devices using manufacturer-provided APIs or software development kits is a plus.</li><li>Familiarity with containerization (Docker, Kubernetes) and CI/CD pipelines (Jenkins, GitHub Actions) is a plus.</li><li>Experience with data analytics and visualization tools (Spotfire, Tableau, Power BI, or Jupyter notebooks) to support data-driven decision-making is a plus.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Host Cell Protein (HCP) Analytics]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49410]]></requisitionid>
    <referencenumber><![CDATA[R49410]]></referencenumber>
    <apijobid><![CDATA[r49410]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49410/associate-scientist-host-cell-protein-hcp-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Associate </strong><strong>Scientist</strong> to join our Product Biochemistry group, supporting our Host Cell Protein (HCP) analytical program. In this role, you will focus on polyclonal antibody purification, ELISA method development, and related reagent generation activities that underpin our HCP impurity monitoring strategy across biologics programs.</p><p>This position offers the opportunity to play a key role in enabling high-quality analytical support for process development, CMC, and regulatory filings, contributing to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site laboratory setting</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support laboratory operations</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Purify polyclonal antibodies from rabbit/goat bleeds immunized with host cell protein antigens, using affinity chromatography and other standard purification workflows</li><li>Optimize and streamline purification protocols to improve yield, purity, reproducibility, and throughput</li><li>Support ELISA method development, qualification, and troubleshooting for HCP detection and quantitation</li><li>Prepare, aliquot, and manage critical reagents (antibodies, conjugates, standards, buffers) to ensure consistent assay performance</li><li>Document all experimental work in the electronic laboratory notebook (ELN) in accordance with defined procedures and departmental standards, and provide documentation upon request to support internal reviews, tech transfer, or regulatory submissions</li><li>Collaborate cross-functionally with process development, QC, and analytical teams to align on reagent needs and assay performance criteria</li><li>Contribute to continuous improvement of laboratory workflows and best practices</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is a hands-on, on-site laboratory role centered on protein purification and immunoassay work, requiring rigorous attention to detail and consistent documentation practices.</li><li>Flexibility to work independently, manage multiple tasks in parallel, and collaborate effectively within a team-oriented environment is required.</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><h3>Must-haves:</h3><ul><li>BS/MS in Biochemistry, Chemistry, Molecular Biology, or a related life science discipline</li><li>Hands-on experience with protein purification (affinity chromatography, e.g., Protein A/G, antigen-affinity columns; AKTA or equivalent FPLC systems preferred)</li><li>Working knowledge of ELISA and general immunoassay techniques</li><li>Ability to work independently, manage multiple tasks in parallel, and maintain rigorous attention to detail</li><li>Excellent written and verbal communication skills; team-oriented mindset</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Prior ELN experience</li><li>Strong documentation habits</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III,  Analytical Science: Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47644]]></requisitionid>
    <referencenumber><![CDATA[R47644]]></referencenumber>
    <apijobid><![CDATA[r47644]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47644/process-development-engineer-iii-analytical-science-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer III</strong> to join our Preclinical Manufacturing & Process Development (PMPD) organization's Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group, on-site in Tarrytown, NY. In this role, you will serve as the analytical lead to develop fit-for-purpose analytical methods, transfer methods, and provide troubleshooting support to advance a diverse bioconjugate pipeline.</p><p>This position offers the opportunity to lead and implement analytical deliverables, working closely with bioconjugation teams and internal/external collaborators (CDMOs) to advance bioconjugate programs from development to commercialization.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site in Tarrytown, NY</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support lab operations and collaboration with internal/external CDMO partners</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Independently design and execute analytical testing, method development, and characterization to enable bioconjugate process development</li><li>Serve as the subject matter expert to lead and design analytical deliverables: robust method development, method transfer to internal/external receiving labs, training, and troubleshooting to move programs forward</li><li>Connect, interpret, and communicate complex results into clear, actionable next steps for technical and non-technical audiences to drive timely decisions</li><li>Author high-quality documentation (e.g., procedures, development and characterization reports, ELN entries) in a timely manner to support program timelines</li><li>Drive, build, and improve business workflows: documentation standardization, data digitization, and sample management</li><li>Maintain compliance with lab and environmental safety requirements and promote a safe lab environment</li><li>Proactively scout, evaluate, and implement new or improved technologies for high-throughput analytics and real-time decision-making</li><li>Lead equipment upkeep and troubleshooting, maintain an organized workspace, and proactively plan for lab resources</li><li>Mentor and support peers and junior team members (direct and/or indirect via matrix)</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is a hands-on, on-site laboratory role serving as analytical lead across bioconjugate programs, requiring close collaboration with internal teams and external CDMO partners and comfort navigating complex, ambiguous problems.</li><li>Flexibility to thrive in a fast-paced, highly collaborative environment while independently driving projects forward is required.</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><h3>Must-haves:</h3><ul><li>B.S. with 10+ years of relevant experience, M.S. with 7+ years, or recent Ph.D. with 0-3 years of relevant experience in chemistry, biochemistry, biology, chemical engineering, or a related field</li><li>Hands-on experience with analytical method development for antibody, bioconjugate, and/or synthetic molecules (e.g., small molecule, PEG, peptides, and/or siRNA), such as electrophoresis, HPLCs, LC-MS, UV spectroscopy, plus associated software (e.g., Empower)</li><li>Hands-on experience transferring methods to internal/external labs, and troubleshooting</li><li>Demonstrated experience serving as an analytical lead for bioconjugate programs, collaborating effectively with internal teams and external CDMOs</li><li>Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences</li><li>Experience drafting analytical methods, development, and characterization reports to support regulatory filing</li><li>Ability to work independently and collaboratively across cross-functional teams to persuade and drive data-based decisions</li><li>Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Customer-centric mindset in providing analytical support across different phases of drug development</li><li>Experience simplifying complex technical messages for varied audiences</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - COLUMBUS, OH]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48898]]></requisitionid>
    <referencenumber><![CDATA[R48898]]></referencenumber>
    <apijobid><![CDATA[r48898]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48898/medical-account-specialist-ii-hematology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Columbus, OH</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Scientist, Product Biochemistry]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49789]]></requisitionid>
    <referencenumber><![CDATA[R49789]]></referencenumber>
    <apijobid><![CDATA[r49789]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49789/assoc-scientist-product-biochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a talented <strong>Associate Scientist</strong> to join our Product Biochemistry group, supporting the characterization, modification, conjugation, purification, and binding analysis of critical reagents used across multiple therapeutic programs, in an on-site capacity. In this role, you will perform advanced characterization of biological reagents using biochemical, biophysical, and binding-based analytical techniques, including Biacore (SPR), to generate high-quality data that supports reagent program needs and lifecycle management, while collaborating with cross-functional teams to support project timelines and reagent-related deliverables.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><strong>Shift Requirements:</strong> Full-time, standard business hours</li><li><strong>Location:</strong> On-site in Tarrytown, NY</li><li><strong>Flexibility & travel:</strong> Minimal to no travel; on-site laboratory presence required to support experimental work and instrumentation needs</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Support the purification, characterization, modification, and conjugation of critical protein and biomolecule reagents using standard analytical methods and laboratory procedures</li><li>Perform advanced characterization of reagents to evaluate identity, purity, stability, aggregation, binding properties, and overall fitness for intended use</li><li>Perform reagent labeling and modification activities to support assay development, method qualification, and reagent supply needs</li><li>Perform binding characterization studies using Surface Plasmon Resonance (SPR) and other analytical platforms to evaluate molecular interactions and reagent performance</li><li>Accurately document laboratory activities, experimental procedures, and analytical results in the electronic laboratory notebook (ELN) following established procedures</li><li>Communicate experimental findings and project updates to the supervisor and team members in a timely manner; summarize results in clear, concise reports and presentations</li><li>Present findings at group meetings and contribute to scientific discussions and problem-solving efforts</li><li>Maintain, troubleshoot, and support laboratory instrumentation necessary for reagent characterization and analytical testing</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is an on-site, hands-on laboratory role requiring the ability to work both independently and within a team on multiple projects simultaneously</li><li>The role includes contributing to lab equipment maintenance and safety practices to help maintain a safe, effective, and efficient working environment</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><h3>Must-haves:</h3><ul><li>BS/MS in Biochemistry, Biophysics, or a related field, with 0–3+ years of experience</li><li>Initiative and drive to complete meaningful tasks and learn new technologies</li><li>Strong organizational, communication, analytical, computer, and technical writing skills</li><li>Excellent oral and written communication skills and evidence of teamwork</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Technical proficiency in automated FPLC and/or HPLC (SEC, IEX, affinity), electrophoresis (capillary or microchip, SDS-PAGE, western blots), spectroscopy, and light scattering</li><li>Fundamental understanding of protein structure/function, protein-protein interaction, and general biochemistry</li><li>Experience working in the biopharmaceutical industry</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Fill Finish Manufacturing, Cleaning Technician]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39745]]></requisitionid>
    <referencenumber><![CDATA[R39745]]></referencenumber>
    <apijobid><![CDATA[r39745]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r39745/supervisor-fill-finish-manufacturing-cleaning-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Cleaning Operations Supervisor to join our Manufacturing team, providing leadership and direction to our Manufacturing Cleaning Technician team while overseeing microbial control across our clean room environments. In this role, you will plan and manage cleaning operations, drive regulatory compliance, and support environmental investigations — while collaborating with Manufacturing, Procurement, and Quality teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Manage all aspects of clean room cleaning operations, including planning, scheduling, and providing work direction to the Manufacturing Cleaning Technician team to ensure ongoing compliance</li><li>Monitor cleaning schedules, progress, data, and work quality; implement the latest clean room technologies by staying current on industry trends</li><li>Conduct troubleshooting and provide support for environmental excursion investigations; monitor liquid and solid waste disposal programs to ensure proper handling and disposal</li><li>Partner with Procurement to manage and maintain vendor contracts in alignment with business needs</li><li>Develop and implement department policies and procedures; ensure effective administration and compliance with regulatory requirements</li><li>Support Manufacturing during regulatory inspections; provide input on long-term planning for processes, staffing, and budget</li><li>Perform personnel management functions including annual performance evaluations, coaching, and employee development</li><li>Experience in clean room operations, environmental monitoring, or manufacturing cleaning in a regulated biopharmaceutical or pharmaceutical environment preferred</li><li>Familiarity with microbial control programs, waste disposal regulations, and environmental monitoring practices</li><li>Demonstrated people leadership experience including scheduling, performance management, and team development</li></ul><p><strong>This role requires:</strong></p><ul><li>3+ years of relevant cGMP experience; BS/BA in Life Sciences or a related field preferred, or equivalent combination of education and experience</li><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lb</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$77,600.00 - $126,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Physician Scientist, Neuroscience & Ophthalmology Genetics]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46973]]></requisitionid>
    <referencenumber><![CDATA[R46973]]></referencenumber>
    <apijobid><![CDATA[r46973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46973/physician-scientist-neuroscience-ophthalmology-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Physician Scientist to join our Neuroscience and Ophthalmology Therapeutic Area Genetics (TAG) team within the Regeneron Genetics Center. In this role, you will translate human genetic evidence into actionable insights across neurological, psychiatric, ophthalmological, hearing-, and aging-related diseases, designing and interpreting large, complex genetic studies while collaborating with Genome Informatics, Analytical Genomics, Clinical Informatics, and other RGC teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY</li><li><strong>Work model/flexibility:</strong> Hybrid</li></ul><br><h3>Discover your role:</h3><ul><li>Apply human genetics to target discovery, indication selection, and identification of patient subgroups likely to respond to treatment</li><li>Design, execute, and interpret genetics studies alongside human genetics scientists, bioinformaticians, and statistical geneticists</li><li>Partner with Therapeutic Area Genetics colleagues and RGC teams to deliver complex, high-quality scientific work</li><li>Generate, summarize, and present findings to internal and external audiences</li><li>Lead or contribute to scientific reports and publications</li><li>Represent the TAG team in cross-functional initiatives across RGC and Regeneron</li><li>Collaborate with external industry and academic partners in scientific consortia</li></ul><br><h3>This role requires:</h3><ul><li>MD or MD/PhD with a strong background in human genetics or genetic epidemiology</li><li>Experience designing and leading human genetics studies that deliver medically relevant findings</li><li>Knowledge of study designs and analyses such as GWAS, exome, or genome sequencing across cohort, case-control, or family-based studies</li><li>Strong communication skills, with the ability to present complex genetic findings to varied audiences</li><li>Familiarity with statistical genetics applications (e.g., polygenic risk scores, quantitative trait analyses, Mendelian randomization) and programming/statistical software (e.g., Python, R) preferred</li><li>Experience integrating genetics with other "omics" technologies (e.g., epigenetics, proteomics, RNA-seq) preferred</li></ul><p>#MDJobs, #MDJobsRGC, #Neurology, #Ophthalmology, #GWAS</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Hematology Oncology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43418]]></requisitionid>
    <referencenumber><![CDATA[R43418]]></referencenumber>
    <apijobid><![CDATA[r43418]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43418/medical-director-clinical-development-hematology-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Sciences to join our Global Clinical Development team, supporting our Hematology Oncology programs. In this role, you will serve as clinical leader for a section of a clinical program, driving execution and clinical deliverables while collaborating with Clinical Scientists, Clinical Operations, Research, Medical Affairs, and external experts including regulatory authorities and key opinion leaders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY or Warren, NJ</li><li><strong>Travel percentage:</strong> 10% to relevant conferences</li></ul><br><h3>Discover your role:</h3><ul><li>Lead clinical strategy and deliverables for an assigned section of a clinical program</li><li>Drive execution across trial phases in partnership with global line functions</li><li>Guide and support assigned Clinical Scientists and Clinical Operations associates</li><li>Represent the program in interactions with regulatory authorities, key opinion leaders, and advisory boards</li><li>Partner cross-functionally with Research, Early Clinical Development, Medical Affairs, Marketing, and HE&OR</li><li>Contribute to internal decision boards shaping program direction</li><li>Shape Global Clinical Development standards by authoring or reviewing SOPs</li><li>Participate in training programs and strategic taskforces that advance clinical development practices</li></ul><br><h3>This role requires:</h3><ul><li>MD or equivalent medical degree with clinical Residency training</li><li>Hematology or Oncology fellowship training strongly preferred</li><li>More than 2 years of experience in clinical research or drug development (academic or industry), spanning Phases I through IV</li><li>Medical/scientific expertise in the disease area of the assigned program, hematologic malignancies, preferred</li></ul><p>#MDJobs, #MDJobsCD, #GDTherapeuticJobs, #Hematology #Oncology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Electrical Project Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46892]]></requisitionid>
    <referencenumber><![CDATA[R46892]]></referencenumber>
    <apijobid><![CDATA[r46892]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46892/senior-electrical-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are seeking a Senior Electrical Engineer who will design, specify and commission new and renovated electrical systems. This individual will provide engineering support and problem solving for new capital projects, existing equipment and manufacturing processes and work in conjunction with the electrical maintenance team to ensure operational availability of electrical distribution networks. </p><p><strong>What you’ll do:</strong></p><ul><li><p>Designing and maintaining LV (e.g. Lighting, General Services, UPS, Protection Settings incl. Arc Flash) and ELV (e.g. Fire Alarm, Data points, Building Automation) systems</p></li><li><p>Managing small projects related to electrical systems infrastructure</p></li><li><p>Assisting in the design review, site acceptance and installation of electrical equipment</p></li><li><p>Preparing and maintaining electrical drawings and related documentation</p></li><li><p>Designing and specifying cGMP E&I equipment and process controls</p></li><li><p>Managing electrical systems residing on the business IT network</p></li><li><p>Supporting validation department by preparation of design documents and assisting in protocol execution</p></li><li><p>Assisting in investigations of equipment and control system anomalies, incl. power quality events</p></li><li><p>Preparing engineering evaluations for and executing modification change control documentation</p></li><li><p>Supervising electrical contractors and confirming works are to the required standard</p></li><li><p>Preparing risk assessments, method statements and all aspects relating to Health and Safety on site</p></li><li><p>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p></li><li><p>Can safely operate and manage HV network</p></li><li><p>Maintaining company reputation by enforcing compliance with all relevant laws, policies, standards and regulations</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>You are skilled at problem-solving and continuous improvement</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>To be considered for this position, you must hold a Bachelors degree in Electrical Engineering or relevant discipline and have 5+ years' experience working in regulated industry. Level will be determined based on qualifications and experience relevant to the role</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>IRELIM #JOBSIEST #LI-Onsite</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement - Direct Materials]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47496]]></requisitionid>
    <referencenumber><![CDATA[R47496]]></referencenumber>
    <apijobid><![CDATA[r47496]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47496/director-global-procurement-direct-materials/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As the Director, Global Procurement you will be developing and leading procurement strategies within the managed spend areas. You will work to build the foundation for continued success in Global Procurement by simplifying, accelerating, and clarifying ways of working. </p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Applying advanced judgement, planning, and independent thought leadership in order to influence positive business program outcomes and drive the procurement team deliverables</p></li><li><p>Either directly, or through a matrix, manages an organization of procurement professionals responsible for carrying out category management and sourcing projects</p></li><li><p>Developing and presenting functional strategy and objectives for procurement in alignment with the category business strategy and operational requirements</p></li><li><p>As part of a business team, influences the strategic direction of how Regeneron employs service providers</p></li><li><p>Directing a team responsible for activities associated with the development and execution of contracts covering spend under management</p></li><li><p>Liaising with finance to ensure all sourcing activities align with Regeneron’s financial controls, ensures ongoing engagement with finance throughout a program’s lifecycle for appropriate levels of contract, savings, and budgetary oversight</p></li><li><p>Providing mentorship, support, and overall leadership to the team to ensure goals are achieved</p></li><li><p>Advises, consults, and drives the global category management program for spend categories under management</p></li><li><p>Reviewing major contracts and acts as an expert resource for planning and leading complex negotiations using leader level mastery skills</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in a relevant area along with 12 years of relevant, progressive experience within procurement, preferably including 9 years directly in sourcing Pharma/Biotech</p></li><li><p>Senior Manager: BS/BA plus 10 years experience</p></li><li><p>Associate Director: BS/BA plus 10 years experience</p></li></ul><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist - Analytical Development, Regeneron Cell Medicines (RCM)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47761]]></requisitionid>
    <referencenumber><![CDATA[R47761]]></referencenumber>
    <apijobid><![CDATA[r47761]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47761/scientist-analytical-development-regeneron-cell-medicines-rcm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Scientist, RCM Analytical Development</strong> to join our Regeneron Cell Medicines (RCM) team. In this role, you will support cell therapy programs by developing, optimizing, and executing biophysical assays to characterize lentiviral vectors, planning and performing experiments, developing new assay protocols, and analyzing and communicating results to advance therapies for patients.</p><p>This position offers the opportunity to partner cross-functionally across RCM to meet program timelines and deliver high-quality analytical data in a fast-paced, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site laboratory setting</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support lab operations, instrument maintenance, and assay execution</li></ul><p><strong>What you'll do:</strong></p><ul><li>Advance analytical development for cell therapy programs, with a primary focus on lentiviral vectors (LVVs)</li><li>Strengthen existing and establish new biophysical methods to characterize LVVs</li><li>Analyze, interpret, and clearly present complex datasets to technical and cross-functional audiences</li><li>Partner with cross-functional teams across RCM to troubleshoot challenges, align on priorities, and support program execution</li><li>Author and review technical documentation, including assay protocols, method development reports, and data summaries</li><li>Maintain complete, timely, and compliant electronic lab notebook records, support instrument upkeep, and independently troubleshoot equipment and assays</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>This is a hands-on, on-site laboratory role focused on biophysical characterization work, requiring independent design and execution of experiments alongside routine laboratory operations and instrument maintenance.</li><li>Flexibility to thrive in a fast-paced, collaborative environment, quickly learn new technologies, and prioritize effectively with minimal supervision is required.</li></ul><p><strong>Let's find out if we're a fit:</strong></p><p>Must-haves:</p><ul><li>Bachelor's or Master's degree in Biophysics, Biochemistry, Molecular Biology, or a related field, with 6-8+ years of proven experience characterizing and quantitatively analyzing lentiviral vectors</li><li>Ability to work independently to design experiments, as well as interpret, document, and communicate results</li><li>Self-motivated and proactive, with the ability to prioritize effectively and drive work forward with minimal supervision</li></ul><p>Preferred / nice-to-haves:</p><ul><li>Experience with biophysical characterization techniques for sizing and counting particles, such as DLS, MRPS, and fluorescent labeling assays</li><li>Understanding and knowledge of viral vector biology, design, process, and gene delivery mechanisms</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44376]]></requisitionid>
    <referencenumber><![CDATA[R44376]]></referencenumber>
    <apijobid><![CDATA[r44376]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44376/director-patent-attorney/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Director, Patent Attorney will act as legal counsel on matters related to the development, protection, and management of Regeneron’s valuable intellectual property pertaining to its manufacturing. The role will be responsible for patent activities relating to manufacturing and bioprocessing at all stages of the development pipeline including cell line technologies, purification, formulations, assay and media development. This position will partner closely with our world-class scientists and manufacturing development leaders around key strategies for our rapidly growing patent portfolio, patent filings, trade secret protection, and patent actions.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Identifying, capturing and prosecuting new inventions relating to manufacturing and bioprocessing; Preparing and prosecuting global patent applications relating to all aspects of manufacturing & bioprocessing including cell development, cell culture, purification, assay development, formulation, packaging and delivery; Leading outside counsel on various projects as appropriate;</p></li><li><p>Conducting patent landscape overviews, freedom-to-operate analyses, validity assessments and patentability assessments in relation to Regeneron pipeline products, and presenting the results and analyses to senior members of the Law Department and senior management;</p></li><li><p>Leading US and foreign administrative patent actions (e.g., oppositions, third party observations, inter partes reviews, etc.);</p></li><li><p>Supporting due diligence projects, agreements and other transactional work, administrative initiatives, and policy questions.</p></li><li><p>Advising on emerging legal issues, including monitoring and reviewing case law and legislative developments.</p></li><li><p>Possess strong interpersonal skills and the ability run multiple projects against competing priorities.</p></li><li><p>Excel at handling a large and sophisticated docket with minimal direction.</p></li><li><p>Have exceptional communication skills, including presentation, interpersonal, writing and conflict resolution.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D. in the life sciences (e.g., biochemistry, molecular biology, cell biology, or related fields)</p></li><li><p>Juris Doctorate from an accredited law school</p></li><li><p>Admitted to practice before the USPTO and licensed to practice law in at least one state (member of the NY bar or eligible for in-house licensure in NY)</p></li><li><p>5- 10 years of proven experience in a law firm setting (with or without corporate law department experience) preparing and prosecuting patent applications in the biological arts.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47030]]></requisitionid>
    <referencenumber><![CDATA[R47030]]></referencenumber>
    <apijobid><![CDATA[r47030]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47030/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Engineer to join our Automation Engineering team, keeping our cutting-edge process controls and process monitoring systems running at peak efficiency. In this role, you will design, develop, and optimize process control and monitoring systems for our sophisticated biopharmaceutical manufacturing processes. You will collaborate closely with Manufacturing, Quality Control, and Facilities teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Troy, NY</li><li>Hours: Monday-Friday 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Design, develop, and implement software and hardware improvements to automated and new equipment under change control.</li><li>Provide PLC- and HMI-based technical support to Manufacturing, Quality Control, and Facilities per established SOPs.</li><li>Troubleshoot and investigate manufacturing deviations tied to automated control systems.</li><li>Develop engineering design documents, technical evaluations, and test plans in line with GAMP 5.</li><li>Support process control and monitoring equipment through software design, commissioning, testing, and corrective action.</li><li>Support small manufacturing, engineering, and validation projects.</li><li>Author and execute Factory Acceptance Test and Site Acceptance Test protocols and system specifications.</li><li>Champion continuous improvement as an everyday mindset, not just a metric.</li></ul><br><h3>This role requires:</h3><ul><li>BS in Engineering or a related field, with 5+ years of relevant experience; equivalent combination of education and experience with process control or data acquisition systems may be considered.</li><li>Experience in the design and maintenance of process control and/or data acquisition systems.</li><li>Experience programming and troubleshooting PLCs; experience with Allen-Bradley and Siemens control system products and video graphic chart recorders is ideal.</li><li>Experience programming and troubleshooting DeltaV DCS is desirable.</li><li>Experience in a regulated manufacturing environment is preferred.</li><li><strong>Gowning and Physical Requirements:</strong></li><li>Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Marketing Manager (Oncology)]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49801]]></requisitionid>
    <referencenumber><![CDATA[R49801]]></referencenumber>
    <apijobid><![CDATA[r49801]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49801/associate-marketing-manager-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>As part of Regeneron’s International Oncology organisation and Italy Oncology Team, you will support brand marketing activities for currently commercialised indications and future launches. Working with cross-functional and cross-regional partners, you will help develop and execute the local country brand plan and deliver customer-focused marketing activities across Italy.</p><br><p><strong>When & where</strong></p><p>Milan (hybrid).</p><br><p><strong>Discover your role</strong></p><ul><li>Support the local country brand planning process by analysing the competitive landscape and identifying key promotional opportunities.</li><li>Develop customer-focused, differentiated messages for key target audiences.</li><li>Partner with Medical Affairs to create and agree an aligned brand strategy.</li><li>Collaborate with cross-functional teams to implement promotional activities within the local country brand plan.</li><li>Analyse brand performance drivers and barriers, including market dynamics and competitive actions, and propose actions to address opportunities or risks.</li><li>Develop and execute external stakeholder engagement plans, including national congresses and healthcare professional meetings.</li><li>Create local promotional materials aligned with local and global brand plans for use by the sales team and through digital channels.</li><li>You manage priorities effectively, act with initiative and creativity, and maintain high ethical and compliance standards.</li></ul><br><p><strong>This role requires</strong></p><ul><li>A bachelor’s degree, preferably in a scientific discipline.</li><li>At least three years of biotech or pharmaceutical brand marketing experience.</li><li>Experience managing agencies and suppliers.</li><li>Working knowledge of local healthcare compliance codes and regulations relating to promotional activities.</li><li>Excellent written and spoken Italian and English, with strong planning, prioritisation, communication and presentation skills.</li><li>Willingness to travel as required, approximately 30–40%, including some weekends for conferences and meetings.</li></ul><br><p>Oncology marketing and launch experience are preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,500.00 - €82,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Regulatory Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49492]]></requisitionid>
    <referencenumber><![CDATA[R49492]]></referencenumber>
    <apijobid><![CDATA[r49492]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49492/associate-manager-regulatory-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Manager </strong>to join our <strong>Regulatory Affairs Advertising and Promotion</strong> team.</p><p>The Associate Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). Provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Associate Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Contribute to the management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Assist with providing timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Assist with providing review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Ability to collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Contributes to the working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Assist with interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, assist with helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; help assess the potential impact of enforcement activities on the company policies.</p></li><li><p>Knowledge of process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Knowledge of products/indications to help provide continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>Knowledge of the input provided during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Ability to understand and work with management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 1 to 2 years within regulatory affairs, preferably within advertising and promotion or completion of a Post-Doctoral Fellowship Program with related experience focused on Regulatory Affairs, including Advertising and Promotion</p></li><li><p>Requires advanced scientific degree (i.e., Masters, PharmD, Ph.D) or at minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences.</p></li><li><p>Fundamental understanding of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products is highly preferred, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is desirable</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and help support launch products/campaigns, while maintaining excellent written/verbal communication skill</p></li><li><p>Familiarity with global promotional review, clinical trial recruitment materials, and labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Research Program Management]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49374]]></requisitionid>
    <referencenumber><![CDATA[R49374]]></referencenumber>
    <apijobid><![CDATA[r49374]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49374/associate-manager-research-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager in Data Operations to join our Research Program Management team, supporting our Discovery organization in an onsite capacity in Tarrytown, NY. In this role, you will strengthen the quality and reliability of discovery portfolio data by leading data operations, quality assurance, and system support activities, while collaborating with Senior Scientific Leadership, Research Program Management, Discovery Scientists, Operational Managers, and IT.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model: Onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Coordinate day-to-day project, program, and portfolio support activities, including tracking work, follow-up, and operational execution.</li><li>Partner with Senior Scientific Leadership, Research Program Management, Discovery Scientists, Operational Managers, and IT to align on data and operational needs.</li><li>Serve as a subject matter expert for assigned data domains, including data structure, business meaning, and downstream impact across the discovery workflow.</li><li>Monitor data quality, investigate issues, and drive corrective actions that improve data accuracy, consistency, and reliability.</li><li>Coordinate data maintenance activities, including backfill, restructuring, and clean-up, to keep discovery portfolio data current and accurate.</li><li>Identify process gaps and improvement opportunities that strengthen data flow, consistency, and operational execution.</li><li>Provide subject matter and technical expertise in PPM systems and tools, including training, testing, and implementation support.</li><li>Support team operational forums and stakeholder touchpoints by communicating needs, surfacing follow-up actions, and maintaining alignment.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelors or Master’s in biology, biochemistry, or another life science-related field and 7+ years of relevant experience (PhD in a related field with relevant work experience preferred but not required).</li><li>Experience supporting discovery operations, data management, system support, or portfolio and operational data processes strongly preferred.</li><li>Working knowledge of data quality, governance standards, and operational processes that support reliable, well-managed data.</li><li>Strong scientific and drug discovery knowledge and connecting data to project, program, and portfolio decisions.</li><li>Experience identifying, analyzing, and helping resolve data issues, including awareness of root cause, downstream impact, and process follow-up needs.</li><li>Strong written, verbal, organizational, and interpersonal communication skills, including the ability to support change management and cross-functional alignment.</li><li>Balancing multiple priorities with discipline, organization, and attention to detail, for both team and personal work.</li><li>A sharp eye for data quality and digging into issues to find root causes and drive lasting fixes</li><li>Strong working relationships across scientific, operational, and technical teams</li><li>Ability to manage multiple priorities with strong organization and attention to detail.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -THOUSAND OAKS, CA / SANTA CLARITA, CA - West]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48078]]></requisitionid>
    <referencenumber><![CDATA[R48078]]></referencenumber>
    <apijobid><![CDATA[r48078]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48078/medical-account-specialist-ii-neurology-thousand-oaks-ca-santa-clarita-ca-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Thousand Oaks]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Thousand Oaks (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Developer – Translational Medicine]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48887]]></requisitionid>
    <referencenumber><![CDATA[R48887]]></referencenumber>
    <apijobid><![CDATA[r48887]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48887/lead-developer-translational-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Business Analyst – Translational Medicine</strong></p><p>The Business Analyst Translational Medicine, will work collaboratively with scientists in the Translational Medicine Research & Preclinical Development section, to document scientific and data processes, including histology and imaging workflows, and contribute to the development of data and technology solutions that support Regeneron’s scientific mission.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Support the translation of business goals and objectives into documented requirements; assist in developing problem statements with guidance from senior team members</p></li><li><p>Document “as is” and “to be” business processes; apply standard methodologies and tools to gather and document functional and non-functional requirements</p></li><li><p>Contribute to mapping information system connections and data flows between systems; assist in identifying data elements and supporting data mapping and data dictionary documentation</p></li><li><p>Apply working knowledge of SQL, Python, AI, and other tools to investigate data; develop familiarity with data lake principles and common database types used in a research environment</p></li><li><p>Assist in maintaining and organizing the backlog of requests; support clear communication of requirements to the development team and help coordinate stakeholder updates</p></li><li><p>Engage with scientists and laboratory personnel to learn and document business processes; support research scientists and technical teams in gathering system and requirements information</p></li><li><p>Help identify data quality issues and support efforts to investigate contributing factors; assist business and IT partners in documenting and communicating findings</p></li><li><p>Handle a variety of tasks across projects, apply sound judgment within defined procedures, and adjust priorities as needed in a dynamic research environment</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Bachelor’s degree in a life science, computer science, information technology, or a related field.</p></li><li><p>2+ years of experience in a research or biotechnology environment.</p></li><li><p>Previous experience in the biotechnology and/or pharmaceutical industry is required. We need someone who has working familiarity with a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, Python programming, agentic tools, data documentation frameworks) and can apply general knowledge of industry practices to support business analysis, requirements gathering, and data flow documentation in a research-focused environment.</p></li><li><p>Previous exposure to laboratory techniques, bioinformatics concepts, relational database principles, or IT software development lifecycle processes is preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[AI/MLOps SRE Lead Engineer]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50034]]></requisitionid>
    <referencenumber><![CDATA[R50034]]></referencenumber>
    <apijobid><![CDATA[r50034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50034/aimlops-sre-lead-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron Digital & Technology, we are expanding our AI and Platform Engineering capabilities to support next-generation intelligent systems, machine learning platforms, and cloud-native technologies. We are seeking an AI-MLOps SRE Lead Engineer to drive reliability, scalability, observability, and operational excellence across our AI, ML, and cloud ecosystem. This role will lead the design and operation of resilient platforms supporting machine learning workloads, LLMs, AI Agents, and enterprise-scale automation while enabling engineering teams to innovate with speed and confidence.</p><p><strong>When & Where</strong></p><p><strong>Hyderabad (Hybrid)</strong></p><p><strong>Discover your role</strong></p><ul><li><p>Drive service reliability, availability, and performance across multi-cloud environments, establishing SLOs, SLIs, error budgets, and reliability standard methodologies.</p></li><li><p>Design, build, and scale enterprise ML platform infrastructure using technologies such as Dataiku, Amazon SageMaker AI, Databricks, and Google Vertex AI.</p></li><li><p>Develop AI-driven observability capabilities using anomaly detection, predictive analytics, and automated remediation solutions to proactively identify and resolve operational issues.</p></li><li><p>Lead the implementation and monitoring of LLM, SLM, RAG, and AI Agent platforms, ensuring performance, governance, operational efficiency, and scalability.</p></li><li><p>Design and implement Infrastructure as Code, CI/CD pipelines, self-healing systems, and platform automation capabilities to improve engineering productivity and operational resilience.</p></li><li><p>Architect enterprise ChatOps solutions that integrate operational events, AI workflows, observability platforms, and automated remediation capabilities.</p></li><li><p>Partner with Data Science, AI Engineering, and Platform teams to deliver secure, scalable, and production-ready AI/ML solutions.</p></li><li><p>Evaluate emerging AI-native operational technologies and integrate innovative solutions that enhance platform reliability, engineering efficiency, and business value.</p></li><li><p>Conduct technical debt assessments, identify architectural risks, and provide strategic recommendations to improve enterprise platform maturity.</p></li><li><p>Serve as a technical leader and trusted advisor, mentoring engineers and influencing reliability engineering, MLOps, and cloud platform strategy across the organization.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Bachelor's degree in Computer Science, Information Technology, Engineering, Data Science, Artificial Intelligence, or a related subject area; Master's degree preferred.</p></li><li><p>6-8 years of experience in Site Reliability Engineering, Platform Engineering, DevOps, or related technology fields with enterprise-scale delivery experience.</p></li><li><p>Strong hands-on experience operating across two or more major cloud platforms, including AWS, GCP, or Azure.</p></li><li><p>Deep expertise with ML platform technologies including Databricks, Amazon SageMaker AI, Dataiku, and Google Vertex AI.</p></li><li><p>Proven experience implementing end-to-end ML workflows including model training, deployment, experiment tracking, monitoring, and pipeline orchestration.</p></li><li><p>Advanced proficiency in Infrastructure as Code tools such as Terraform, Pulumi, AWS CDK, and modern CI/CD automation practices.</p></li><li><p>Strong programming and scripting skills in Python, Go, Bash, or similar languages.</p></li><li><p>Experience building enterprise observability solutions using Prometheus, Grafana, Datadog, OpenTelemetry, distributed tracing, metrics, and logging platforms.</p></li><li><p>Demonstrated expertise in anomaly detection, predictive analytics, automated remediation, and AI-assisted operational capabilities.</p></li><li><p>Proven experience designing and implementing enterprise ChatOps solutions and AI-enabled operational workflows.</p></li><li><p>Strong ability to assess technical debt, influence technical strategy, and drive platform modernization initiatives.</p></li><li><p>Experience using AI tools, LLM-powered assistants, and AI Agents to enhance engineering operations and productivity.</p></li><li><p>Experience with Kubernetes and container orchestration platforms such as EKS, GKE, or AKS preferred.</p></li><li><p>Familiarity with MLOps technologies including Kubeflow, Feast, MLflow, and model evaluation frameworks such as LangSmith, RAGAS, Evidently AI, or Weights & Biases preferred.</p></li><li><p>Knowledge of cloud cost optimization, policy-as-code, compliance automation, and multi-cloud governance practices preferred.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[VP, Global Patient Safety Sciences, General Medicine]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47607]]></requisitionid>
    <referencenumber><![CDATA[R47607]]></referencenumber>
    <apijobid><![CDATA[r47607]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47607/vp-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>VP, Global Patient Safety Sciences – General Medicine</strong></p><p> <br>The VP, Global Patient Safety Sciences (GPS) – General Medicine serves as the primary point of contact for General Medicine safety strategy across clinical and post‑marketing assets. As the Therapeutic Area Head (TAH) and product subject matter expert (SME), you define safety strategy, establish the medical safety opinion, and provide the scientific point‑of‑view across GPS and non‑GPS interactions. You will advise senior leadership on safety strategies and processes, shape cross‑functional decisions, and serve on the GPS Leadership Team (GPS LT). This role also leads and develops a high‑performing team.</p><p><strong>In This Role, You Will:</strong></p><p><strong>Safety Strategy & Clinical Risk Assessment</strong></p><ul><li>Contribute senior‑level safety expertise to clinical programs across the assigned therapeutic area.</li><li>Serve as the medical review resource for complex Individual Case Safety Reports (ICSRs) and other data sources; act as point of escalation for ICSR causality assessments.</li><li>Oversee safety signal evaluations and deliver clinical interpretation of emerging safety issues.</li><li>Review benefit‑risk assessments (e.g., HHAs) and provide recommendations appropriate to asset lifecycle stage, including responses to health authority queries and safety documents (e.g., DSURs, PSURs).</li><li>Develop innovative approaches to core safety activities that integrate new technologies, including AI.</li></ul><p><strong>Governance Leadership</strong></p><ul><li>Influence cross‑functional leaders to align priorities and drive enterprise outcomes.</li><li>Approve and provide medical oversight for Risk Management Plans (RMPs).</li><li>Approve responses to medical and clinical health authority queries as needed.</li><li>Oversee cross‑functional Safety Monitoring Team (SMT) activities.</li><li>Represent GPS at governance forums, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT), and with external collaborators.</li></ul><p><strong>Talent Development & Organizational Leadership</strong></p><ul><li>Build, coach, and scale a high‑performing team; drive succession planning and talent pipelines.</li><li>Lead talent strategy and leadership development initiatives to strengthen organizational capabilities.</li></ul><p><strong>What You Need to Succeed</strong></p><p><strong>Required Qualifications</strong></p><ul><li>15+ years of pharmacovigilance (PV) or relevant clinical experience in the pharmaceutical/biotech industry.</li><li>8+ years of people leadership with demonstrated success leading teams; experience in a matrixed environment is a plus.</li><li>Proven ability to develop a deep understanding of product safety profiles to inform safety assessments, risk evaluations, and decision‑making.</li><li>Experience overseeing strategy within a global patient safety organization.</li><li>Strong leadership presence with excellent interpersonal, verbal, and written communication skills.</li><li>Advanced organizational and workload planning skills with the ability to manage multiple projects simultaneously.</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Minimum 5 years of international pharmaceutical activities.</li><li>Advanced degree preferred: M.D., PA, or PharmD; Board Certification or equivalent in a relevant clinical specialty; MBA is an advantage.</li><li>Experience with AI technologies applied to safety science.</li></ul><p><strong>Work Model</strong></p><ul><li>This role requires 4+ days per week on‑site presence.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Clinical Trial Services, India]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47672]]></requisitionid>
    <referencenumber><![CDATA[R47672]]></referencenumber>
    <apijobid><![CDATA[r47672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47672/director-global-clinical-trial-services-india/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Global Clinical Trial Services, India to join our Global Clinical Trial Services team, supporting our India operations. In this role, you will provide operational leadership for clinical trial delivery in India as part of the senior leadership team, ensuring high-quality and compliant execution while collaborating with global functional leaders, site management, and vendor partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Hyderabad, India.</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead clinical trial services in India, from feasibility through to site close.</p></li><li><p>Manage and develop India-based staff and Functional Service Provider (FSP) teams.</p></li><li><p>Partner with global functional leaders to align India operations with worldwide standards.</p></li><li><p>Build relationships with local sites, investigators, and regulatory authorities.</p></li><li><p>Champion clinical trial infrastructure development in India alongside site management.</p></li><li><p>Oversee FSP resource planning, contracts, and vendor performance.</p></li><li><p>You connect regional and global teams through clear, cross-cultural communication.</p></li><li><p>You drive process improvements and standard methodologies while upholding compliance.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Deep understanding of the Indian clinical research landscape and regulatory environment.</p></li><li><p>Knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and Indian regulations.</p></li><li><p>Proven leadership in a matrix organisation with dotted-line reporting.</p></li><li><p>Strong experience in resource planning, vendor management, and operational budgeting.</p></li><li><p>Familiarity with site management, site start-up, trial optimisation, and central monitoring.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CHICAGO South, IL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48051]]></requisitionid>
    <referencenumber><![CDATA[R48051]]></referencenumber>
    <apijobid><![CDATA[r48051]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48051/medical-account-specialist-ii-neurology-chicago-south-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Chicago South (Metro), Illinois </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II Neurology - DETROIT South, MI]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48048]]></requisitionid>
    <referencenumber><![CDATA[R48048]]></referencenumber>
    <apijobid><![CDATA[r48048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48048/medical-account-specialist-ii-neurology-detroit-south-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Detroit]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Detroit South (Metro), Michigan </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - DALLAS, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48059]]></requisitionid>
    <referencenumber><![CDATA[R48059]]></referencenumber>
    <apijobid><![CDATA[r48059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48059/medical-account-specialist-ii-neurology-dallas-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dallas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Dallas (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - HOUSTON (SOUTH), TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48061]]></requisitionid>
    <referencenumber><![CDATA[R48061]]></referencenumber>
    <apijobid><![CDATA[r48061]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48061/medical-account-specialist-ii-neurology-houston-south-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><p><strong>When & where: </strong> </p><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Houston South (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II -  NEUROLOGY -SAN DIEGO, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48081]]></requisitionid>
    <referencenumber><![CDATA[R48081]]></referencenumber>
    <apijobid><![CDATA[r48081]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48081/medical-account-specialist-ii-neurology-san-diego-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Diego]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: San Diego (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PITTSBURGH, PA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48005]]></requisitionid>
    <referencenumber><![CDATA[R48005]]></referencenumber>
    <apijobid><![CDATA[r48005]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48005/medical-account-specialist-ii-neurology-pittsburgh-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Pittsburgh]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Pittsburg (Metro), PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - INDIANAPOLIS, IN]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48052]]></requisitionid>
    <referencenumber><![CDATA[R48052]]></referencenumber>
    <apijobid><![CDATA[r48052]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48052/medical-account-specialist-ii-neurology-indianapolis-in/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Indianapolis]]></city>
    <state><![CDATA[Indiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Indianapolis (Metro), Indiana </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHOENIX N, AZ]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48071]]></requisitionid>
    <referencenumber><![CDATA[R48071]]></referencenumber>
    <apijobid><![CDATA[r48071]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48071/medical-account-specialist-ii-neurology-phoenix-n-az/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Pheonix (North Metro), AZ</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - SALT LAKE CITY, UT]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48073]]></requisitionid>
    <referencenumber><![CDATA[R48073]]></referencenumber>
    <apijobid><![CDATA[r48073]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48073/medical-account-specialist-ii-neurology-salt-lake-city-ut/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Salt Lake City]]></city>
    <state><![CDATA[Utah]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Salt Lake City (Metro), UT</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - WASHINGTON, DC]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48016]]></requisitionid>
    <referencenumber><![CDATA[R48016]]></referencenumber>
    <apijobid><![CDATA[r48016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48016/medical-account-specialist-ii-neurology-washington-dc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Washington]]></city>
    <state><![CDATA[District of Columbia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Washington, DC (Metro)</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Pathologist]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47855]]></requisitionid>
    <referencenumber><![CDATA[R47855]]></referencenumber>
    <apijobid><![CDATA[r47855]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47855/associate-director-clinical-pathologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Clinical Pathology support to selected TFAs, and mentor junior Pathologists. </p></div><div></div><div><p><strong>A Typical day in this role may look like:</strong> </p></div><div><ul><li><p>Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas. </p></li></ul></div><div><ul><li><p>Work both independently and as a part of integrated discovery and development teams to interpret pharmacologic and toxicity related findings and help advance promising therapeutics through Regeneron’s pipeline. </p></li></ul></div><div><ul><li><p>Determining and evaluating clinical pathology-related endpoints in pharmacology and toxicology studies and guiding decision making. </p></li></ul></div><div><ul><li><p>Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron. </p></li></ul></div><div><ul><li><p>Partner with our CRO partners in providing scientific peer review of nonclinical safety studies. </p></li></ul></div><div></div><div><p><strong>This job might be for you if you have:</strong> </p></div><div><ul><li><p>Experience with integrating clinical and anatomic pathology data </p></li></ul></div><div><ul><li><p>Experience with animal models of human diseases </p></li></ul></div><div><ul><li><p>Clear, concise oral and written communication skills </p></li></ul></div><div><ul><li><p>Demonstrated ability to contribute to cross functional teams </p></li></ul></div><div><ul><li><p>Ability to contribute to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes. </p></li></ul></div><div></div><div><p><strong>In order to be considered for this role, you must have</strong>: </p></div><div><ul><li>DVM (or equivalent) with ACVP certification in Clinical Pathology required, (strong preference for PhD in Pathology, Immunology, or related ) </li></ul></div><div><ul><li>Minimum 3 years of industry experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/ biotech or CRO setting. </li><li>Additional certification in Anatomic Pathology nice to have</li></ul></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager - Full Stack Developer- Clinical Data Operation]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47963]]></requisitionid>
    <referencenumber><![CDATA[R47963]]></referencenumber>
    <apijobid><![CDATA[r47963]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47963/senior-manager-full-stack-developer-clinical-data-operation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>As a Senior Manager – Clinical Data Solutions & Insights, you will be responsible for designing, building, and handling a centralized clinical reporting platform that consolidates reporting outputs across Data Management and external vendor reconciliation activities into a single governed reporting layer. This role will be responsible for the end-to-end reporting lifecycle including data ingestion, analytical dataset development, dashboard creation, automated reporting, and self-service analytics applications using modern visualization and web technologies. You will work closely with Clinical Sciences, Data Management, Pharmacometrics, Precision Medicine, Safety, and multi-functional collaborators to deliver intuitive, audit-ready reporting solutions that support data-driven decision making, regulatory compliance, and operational perfection.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong></p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Owning the design and delivery of a centralized clinical reporting platform consolidating EDC listings, exception reports, and vendor reconciliation outputs</p></li><li><p>Building and maintaining Clean Patient Tracker applications providing real-time access to CRF completion, visit status, data queries, freeze/lock status, and PI signature status</p></li><li><p>Developing executive-level dashboards highlighting portfolio-wide KPIs such as query aging, protocol deviations, data entry lag, and study completion achievements</p></li><li><p>Partnering with Data Management Reporting teams and external vendor delivery teams to establish structured data ingestion pipelines for EDC and reconciliation reports</p></li><li><p>Collaborating with Clinical Sciences, Biostatistics, Safety, and Precision Medicine teams to develop validated self-service analytical tools and reporting applications</p></li><li><p>Designing and implementing data visualization standards, UX/UI guidelines, and reporting procedures for non-technical stakeholders</p></li><li><p>Building curated analytical datasets and semantic layers connected to clinical data lakes and vendor reconciliation feeds</p></li><li><p>Running the full reporting lifecycle including requirements gathering, UX wireframing, development, validation, UAT coordination, and production deployment</p></li><li><p>Driving automation across routine reporting workflows including scheduled data ingestion, reconciliation report generation, and alert-based notifications</p></li><li><p>Supporting GCP compliance, inspection readiness, report governance, version control, and audit trail management</p></li><li><p>Driving adoption of reporting tools through stakeholder engagement, training, and change management initiatives</p></li><li><p>Serving as an SME for clinical data reporting, embedded analytics, and emerging visualization technologies</p></li></ul><p><strong>This Role May Be For You If You Have:</strong></p><ul><li><p>Demonstrable experience in Clinical Data Management, clinical trial reporting, analytics, or reporting platform development</p></li><li><p>Hands-on experience with Medidata Rave EDC including query management workflows and dataset structures</p></li><li><p>Solid understanding of CDISC CDASH/SDTM standards and GxP/CSV validation principles</p></li><li><p>Experience developing reporting applications using Python frameworks such as Dash, Streamlit, or Flask</p></li><li><p>Demonstrable experience with Power BI, Tableau, SQL, and analytical dataset development</p></li><li><p>Experience working with clinical data sources, clinical metrics, and external vendor reconciliation outputs</p></li><li><p>Strong UX/UI design sensibility for building intuitive reporting tools for non-technical users</p></li><li><p>Excellent stakeholder management, communication, and presentation skills</p></li><li><p>Strong analytical thinking and problem-solving capabilities</p></li><li><p>Ability to work optimally in a fast-paced, matrixed, and multi-functional environment</p></li></ul><p><strong>To Be Considered For This Role, You Must Have:</strong></p><ul><li><p>8+ years of experience in Clinical Data Management or clinical trial operations</p></li><li><p>Minimum 3+ years focused on clinical data reporting, analytics, or reporting tool development</p></li><li><p>Experience with clinical reporting applications, dashboards, and data visualization tools</p></li><li><p>Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field</p></li><li><p>Advanced degree (MBA/MS) preferred</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Indirect Category Management]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48238]]></requisitionid>
    <referencenumber><![CDATA[R48238]]></referencenumber>
    <apijobid><![CDATA[r48238]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48238/manager-indirect-category-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Indirect Category Management Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will lead category management enablement, transform data and market intelligence into actionable insights, and support global indirect category strategies while collaborating with global procurement teams, data and analytics partners, and key collaborators. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead a team of associates and specialists transforming internal and external analytics into insights that enable global indirect category management strategies.</p></li><li><p>Support the definition and implementation of global indirect category strategies aligned to regional and global business needs.</p></li><li><p>Deliver micro and macro market analysis, spend analysis, supplier evaluation, and risk insights to support strategy development and partner engagement.</p></li><li><p>Partner with data and analytics teams to demonstrate internal and external data sources to identify trends, opportunities, and forecast future strategy direction.</p></li><li><p>Facilitate sourcing processes by preparing RFPs, RFQs, and RFIs and managing response collection, analysis, and comparative evaluation across sourcing and SRM events.</p></li><li><p>Maintain, standardize, and optimize category management templates, strategy decks, and stage-gate materials while improving procurement tools and repositories.</p></li><li><p>Lead contract management activities, oversee team execution, and track and report category management enablement requests in line with engagement plans.</p></li><li><p>You build strong relationships, lead through influence, and operate with integrity and clarity in a global, matrixed, and evolving environment.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive procurement experience; Pharma/Biopharma experience preferred.</p></li><li><p>Proven experience leading teams, processes, and suppliers across a breadth of categories in a multinational environment.</p></li><li><p>Strong expertise in category management principles including market analysis, spend analysis, supplier evaluation, and risk management.</p></li><li><p>Experience transforming data and market intelligence into actionable insights to enable category strategies.</p></li><li><p>Experience managing and developing associate and specialist-level professionals, including performance management, coaching, and career development.</p></li><li><p>Ability to build influential relationships with collaborators and suppliers to get results .</p></li><li><p>Experience in contract management and supporting sourcing and supplier relationship management activities.</p></li><li><p>Working knowledge of ERP systems such as Oracle and Source-to-Pay platforms (Oracle, Zycus, GEP, Ariba, or similar) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint).</p></li><li><p>Ability to operate with integrity, focus, and clarity in ambiguous environments and inspire change and continuous improvement .</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Manager - Engineering & Automation]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48600]]></requisitionid>
    <referencenumber><![CDATA[R48600]]></referencenumber>
    <apijobid><![CDATA[r48600]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48600/senior-project-manager-engineering-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>We are looking for an experienced Project Manager to join our growing team! The Senior Project Manager—Engineering & Automation will apply technical skills and resources to deliver impact quickly, without compromising quality, and manage stakeholder expectations to ensure technological development & implementation projects that bring value aligned with cGMP procedural requirements and strategic goals of Regeneron’s Industrial Operation and Product Supply organization. You will efficiently allocate resources and monitor progress by tracking key performance indicators against specific business processes.</p><br><h3>When & where:</h3><ul><li>Monday-Friday 8:00am-4:30pm</li><li>Troy, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Capitalize on technical background and knowledge of project management principles to deliver strategic value through oversight of complex, interdependent cGMP technology and equipment implementations.</li><li>Ensure key technical resources are in place to achieve project deliverables, optimizing them with iterative, feedback-driven processes.</li><li>Lead teams, streamlining stakeholder communication, and resolving conflicts with approaches tailored to improve speed-to-value.</li><li>Ensure SDLC processes and implementations are applied to desired project outcomes.</li><li>Develop automated dashboards to report project performance, tracked by timely, strategic goal-oriented key performance indicator assessment.</li><li>Minimize project complexity through risk identification and mitigation tactics, efficiently allocating resources, and monitoring progress by tracking key performance indicators.</li><li>Use data analytics and supportive AI to forecast business impact and streamline decision-making.</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA in Science/Engineering or a related technical field along with 10+ years of relevant experience in an Engineering, Automation, or Information Technology setting.</li><li>Direct experience in a pharmaceutical or biopharmaceutical manufacturing facility, with a high level of proficiency in project management within a portfolio management framework, as well as computerized system procurement, design, installation, and support in a cGMP industrial setting.</li><li>Strong knowledge and experience of Change Management in a GxP environment.</li><li>Detailed understanding of bioprocessing equipment design and GxP software quality system principles, with a focus on data integrity.</li><li>Broad business acumen and understanding of how to apply system development lifecycle concepts to computerized assets implemented globally for qualified use in a GxP environment.</li><li>Advanced portfolio/program/project management experience.</li><li>Ability to develop & publish schedules, dashboards, reports, and other project documents using project planning tools such as MS Project, Azure DevOps, Jira, etc.</li><li>Excellent communication (verbal and written), analytical and problem-solving skills, demonstrating creative and independent reasoning to navigate scope, time, and cost constraints, assuring quality deliverables.</li><li>Knowledge and experience with the design, development, configuration, and implementation of computerized equipment and systems for cGMP use is preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$141,400.00 - $231,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - OKLAHOMA CITY, OK - Mountain West]]></title>
    <date><![CDATA[Sun, 12 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48069]]></requisitionid>
    <referencenumber><![CDATA[R48069]]></referencenumber>
    <apijobid><![CDATA[r48069]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48069/medical-account-specialist-ii-neurology-oklahoma-city-ok-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Oklahoma City]]></city>
    <state><![CDATA[Oklahoma]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Oklahoma City (Metro), Oklahoma </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Precision Medicine (Cell Medicine)]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46672]]></requisitionid>
    <referencenumber><![CDATA[R46672]]></referencenumber>
    <apijobid><![CDATA[r46672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46672/director-precision-medicine-cell-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>We are seeking to hire a Precision Medicine Scientific Lead to oversee the development and execution of biomarker strategies for novel cell therapies, cell transfer conditioning agents and combinations with bispecific antibodies across multiple disease areas (Oncology and Immunology). In this highly matrixed role, they will design, develop, communicate across levels and operationally implement clinical biomarker strategies to support selecet programs in early and late stage drug development. Clinical biomarker assays include pharmacokinetic assays, mechanism of action, patient stratification assays and pharmacodynamic assays. The candidate will collaborate with teams internal to RCM and more broadly Regeneron or with contract research organizations to develop and implement clinical biomarker assays.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Cambridge, MA or Tarrytown, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Program-level Precision Medicine lead that develops and implements the strategic vision for pharmacokinetic, pharmacodynamic, and exploratory biomarkers for clinical studies enabling indication and/or patient selection, early indication of biological activity, and to identify potential novel combinations.</p></li><li><p>String collaboration with Biomarker and clinical operation teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Key individual contributor and precision medicine representative to development and Cell therapy characterization teams with a remit to integrate, influence and deliver biomarker strategies from initial concept to execution, data delivery and results interpretation.</p></li><li><p>Collaborate with internal Regeneron laboratories and groups (e.g. BioAnalytical, Clinical Pharmacology, Molecular Profiling, CDX, Discovery Research, Analytical Innovations, DMSQ etc.) to develop plan for validation and application of assays in the clinic.</p></li><li><p>Accountability for ensuring complex clinical assays used in programs are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine biomarker strategies for molecules in discovery phases (leading to candidate molecule selection) through to the clinic.</p></li><li><p>Represent Regeneron externally thorough collaborations and/or presentations.</p></li><li><p>Contribute to Clinical Protocol, schedule of Assessments, clinical study reports, technical reports, data agreements, scientific publications and make recommendations to development teams and management</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD and 10+ years of experience participating effectively on cross-disciplinary teams in pharmaceutical or biotech industry.</p></li><li><p>Experience in clinical assay development, validation and implementation with strong experience in Immunology is preferred.</p></li><li><p>The ability to drive, manage, complete and deliver results for complex multi-functional projects</p></li><li><p>Excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Precision Medicine Operations]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48614]]></requisitionid>
    <referencenumber><![CDATA[R48614]]></referencenumber>
    <apijobid><![CDATA[r48614]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48614/manager-precision-medicine-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><div><div><div><div><div><div><div><div><div></div></div></div></div></div></div></div></div></div><p>The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology. In this role, you will be a key driver of precision medicine operational execution partnering with Precision Medicine Strategy Lead (PMSL), clinical study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL), Clinical Laboratory Study Manager (CLSM), and Clinical Laboratory Project Management (CLPM) groups to deliver high-quality samples and data. Through strong cross functional collaboration and operational excellence, you will help ensure biomarker and non-biomarker strategies are executed seamlessly, enabling the translation of innovative science to medicines for patients.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY or Warren, NJ</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Works with project manager and set-up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics</p></li><li><p>Monitor’s acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensure compliance with ICF permissions</p></li><li><p>Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing </p></li><li><p>Work closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries.</p></li><li><p>Oversees Study start up, closeout and overall life-cycle activities for assigned studies at central lab/specialty labs to support all samples and testing</p></li><li><p>Provides input on sample-related section in clinical trial-related (e.g. protocols and ICF) and other supporting documents</p></li><li><p>Works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials.</p></li><li><p>Enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor's degree with a minimum of 8 years of pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams.</p></li><li><p>Minimum of 5 years' experience with Clinical Trials, focus on clinical sample collection</p></li><li><p>Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested.</p></li><li><p>Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Corporate Counsel, Corporate Governance]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48604]]></requisitionid>
    <referencenumber><![CDATA[R48604]]></referencenumber>
    <apijobid><![CDATA[r48604]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48604/director-corporate-counsel-corporate-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>Regeneron’s Corporate Governance & Securities Team is seeking an experienced attorney to serve as a strategic and solutions-oriented partner supporting our rapidly growing and globally expanding business. In this role, you will provide proactive legal advice on global subsidiary management, corporate governance, and general corporate matters. You may also be involved in providing legal support on public company reporting, securities law compliance, treasury/financing matters, and corporate transactions. You will be an integral member of a collaborative, agile Law Department that partners closely with key internal clients including Tax, Finance, Treasury, and Accounting/Financial Reporting.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Serve as a dedicated resource for global subsidiary management, supporting Regeneron’s approximately 30 domestic and international subsidiaries across a range of legal and corporate governance requirements, including statutory financial statement audits, corporate filings, and banking mandates, while coordinating closely with Regeneron Tax, Finance, Treasury, and Accounting/Financial Reporting teams.</p></li><li><p>Manage and maintain Regeneron’s cloud-based corporate document database (hCue), ensuring data integrity and accessibility of corporate records.</p></li><li><p>Draft and maintain shareholder and board resolutions, consents, agendas, secretary’s certificates, and other records. </p></li><li><p>Provide legal advice regarding certain intercompany transactions, including intercompany financing arrangements. </p></li><li><p>Assist with shareholder/equityholder meeting matters for Regeneron’s subsidiaries.</p></li><li><p>Assist in connection with board and committee meetings for Regeneron’s subsidiaries.</p></li><li><p>Oversee the formation and setup of future domestic and international subsidiaries. Work across international jurisdictions and cross-functional teams, with the ability to manage competing priorities and reduce reliance on outside counsel.</p></li><li><p>Assist other legal matters in which the Corporate Governance & Securities team is involved from time to time, such as preparation of current and periodic reports to the SEC, including Forms 10-K, Forms 10-Q, and Forms 8-K; Section 16 reporting; financing matters and legal support of the treasury function; and corporate transactions.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>JD with excellent law school credentials. </p></li><li><p>Licensed to practice law in New York, or eligible for licensure as registered in-house counsel in New York. </p></li><li><p>8–10 years of experience in SEC reporting, public company compliance, corporate governance, and/or global subsidiary management. </p></li><li><p>Experience with international subsidiary management and cross-border corporate governance matters is a strong plus. </p></li><li><p>Law-firm training preferred; prior in-house experience a plus.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Legal Data Privacy Operations]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47119]]></requisitionid>
    <referencenumber><![CDATA[R47119]]></referencenumber>
    <apijobid><![CDATA[r47119]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47119/senior-manager-legal-data-privacy-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>Regeneron is seeking an experienced and forward-thinking Senior Manager Legal Data Privacy Operations to lead privacy program operations within the Law Department / Privacy Office. As a key member of the Privacy Office within Regeneron’s Law Department, you will play an important role in advancing our data privacy program. This includes managing complex privacy projects, delivering tactical operational support, and supporting governance initiatives. By leading well-designed and executed privacy operations, this role plays a central part in building the organizational foundation that enables Regeneron to manage data responsibly, maintain trust, and support the company's overall mission.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Managing and identifying opportunities to improve core privacy operations, including Privacy Impact Assessment, Record of Processing Activities, and Data Subject Access Request processes across multiple business units, geographies, and regulatory frameworks.</p></li><li><p>Leading complex privacy program initiatives that involve coordinating and aligning privacy processes with other business functions and leveraging technology and AI to automate, find efficiencies, and enhance how privacy operations are managed and executed.</p></li><li><p>Documenting advice and implementation of online privacy notices and controls, tracking technologies, and privacy-enhancing tools.</p></li><li><p>Developing and maintaining privacy program metrics and KPIs.</p></li><li><p>Maintaining and developing internal policies, procedures, guidance documents, training and awareness, including our Intranet site.</p></li><li><p>Coordinating Privacy Steward engagement to advance enterprise-wide privacy initiatives in alignment with organizational objectives and regulatory requirements.</p></li><li><p>Managing vendor relationships by overseeing the execution of Statements of Work and ensuring timely processing of requisitions, purchase orders, and invoices.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A bachelor's degree, advanced degree in a related field preferred.</p></li><li><p>At least 8 years of experience in privacy, with a preference for at least 3 years managing privacy operations within a legal or compliance privacy function.</p></li><li><p>Certified Information Privacy Manager (CIPM) or Certified Information Privacy Technologist (CIPT) Project Management Professional (PMP) or equivalent certification.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Commercial Insights & Analytics]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48854]]></requisitionid>
    <referencenumber><![CDATA[R48854]]></referencenumber>
    <apijobid><![CDATA[r48854]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48854/associate-director-commercial-insights-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Associate Director, Commercial Insights & Analytics International</h3><p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Commercial Insights & Analytics International to join our Commercial Insights and Analytics team, supporting Neurology across Europe, Japan and Canada in a hybrid model. In this role, you will enable informed decision making while collaborating with above-market teams, local teams, IT, sourcing and vendors.</p><p>Reporting to the Director, Insights and Analytics International, this position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Paris - supporting international markets across Europe, Japan and Canada.</p><p>Hybrid work model - Office based</p><br><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Be responsible for international performance analytics and reporting for evolving business needs.</li><li>Lead customer insights, market research and reporting deliverables for Neurology.</li><li>Implement above-country market research and objective secondary data analyses.</li><li>Build patient cohorts, treatment journeys and patient flow forecasts.</li><li>Develop account-level insights, including segmentation and opportunity assessments.</li><li>Partner with Commercial Operations on field sizing, targeting and incentive analyses.</li><li>Centralize data management needs with business leaders, IT and sourcing.</li><li>You create clear insights that connect business implications with practical options.</li></ul><br><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>8+ years of relevant experience, including 4+ years in market research.</li><li>Above-country analytics and market research experience in international pharmaceutical markets.</li><li>Understanding of biopharmaceutical commercial dynamics, laws and regulations.</li><li>Knowledge of data industry standards and data asset procedures.</li><li>Expertise in data visualization, data storytelling and report creation tools.</li><li>Proficiency in Microsoft PowerPoint, Excel, Word and Veeva.</li><li>Practical experience with Power BI, QlikView, Tableau, Oracle BI, MicroStrategy, Cognos or Spotfire.</li><li>Strong project, change management, presentation, communication and collaboration skills.</li><li>English language skills; with one additional language including German, French, Italian or Japanese preferred.</li><li>Prior biopharmaceutical field sales or marketing experience is desirable.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€84,675.00 - €141,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Statistical Programming]]></title>
    <date><![CDATA[Fri, 17 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48840]]></requisitionid>
    <referencenumber><![CDATA[R48840]]></referencenumber>
    <apijobid><![CDATA[r48840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48840/associate-director-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Statistical Programming to join our Statistical Programming team, supporting our therapeutic area programs in a hybrid work model. In this role, you will oversee statistical programming activities across internal teams and functional service providers, ensuring high-quality deliverables while shaping departmental standards, processes, and training. You'll collaborate closely with study and project teams, programming leadership, and cross-functional stakeholders to meet therapeutic analysis and computing needs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ</li><li>Work model/flexibility: Onsite/hybrid</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead and manage a statistical programming group, driving timely, high-quality deliverables across internal and outsourced work</li><li>Shape and implement programming standards, applications, processes, and training for your therapeutic area</li><li>Partner with study and project teams to clarify requirements and guide programmers through assignment execution</li><li>Represent Statistical Programming with partnering functions to ensure specifications and computing needs are met</li><li>Champion company values, modeling excellence, collaboration, ownership, and accountability</li><li>Drive department goals and lead subject-matter-expert initiatives</li><li>Set goals, manage performance, and mentor direct reports, supporting their growth and development</li><li>Contribute to hiring by screening and interviewing programming candidates</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Bring proven experience managing programming teams and external service providers</li><li>Think strategically about department-wide standards, processes, and long-term goals</li><li>Communicate confidently across global, cross-functional teams</li><li>Solve problems independently and manage multiple priorities under tight timelines</li><li>Enjoy mentoring and developing junior staff and contractors</li><li>Take ownership of deliverables without close supervision</li><li>Bring a collaborative, respectful, and solutions-oriented mindset to complex projects</li></ul><p><strong>This role requires:</strong></p><ul><li>Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline, with 10+ years of clinical programming experience</li><li>Advanced SAS programming skills (Base, Stat, Macro, Graph) within a clinical data environment</li><li>Demonstrated project and people management experience, including work across global, interdisciplinary teams</li><li>Expertise in one or more therapeutic areas and strong understanding of pharmaceutical clinical development and regulatory submissions</li></ul><p><strong>Nice to haves:</strong></p><ul><li>SAS certification</li><li>Leadership experience supporting the hiring, development, and evaluation of junior staff and contractors</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, Advanced Therapy Project Management (ATPM)]]></title>
    <date><![CDATA[Mon, 20 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47142]]></requisitionid>
    <referencenumber><![CDATA[R47142]]></referencenumber>
    <apijobid><![CDATA[r47142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47142/process-development-engineer-ii-advanced-therapy-project-management-atpm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Associate</strong> to join our Advanced Therapy Project Management (AT-PM) group within Product, Analytical, and Process Development Operations (PAPD Ops) in an on-site capacity. In this role, you will support project management, technology transfer, and business operations for Regeneron's Advanced Therapy Programs, helping drive successful development and tech transfer of advanced therapies (e.g., AAV, bioconjugates, and synthetic chemistry programs), while collaborating with internal partners and Contract Development & Manufacturing Organizations (CDMOs) to enable clear cross-functional ways of working and operational excellence.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: On-site in Tarrytown, NY</li><li>Work model/flexibility: Onsite, full-time</li></ul><h3>What you'll do:</h3><ul><li>Lead cross-functional tech transfer teams and independently own workstreams to establish production processes at CDMOs</li><li>Drive readiness for manufacturing start-up by clarifying scope, securing inputs and approvals, tracking deliverables, and escalating risks with proposed mitigations</li><li>Own communication strategy and operating cadence for assigned programs, providing concise, decision-ready status reporting to audiences ranging from core teams to senior stakeholders</li><li>Build, maintain, and continuously improve integrated plans across development and transfer activities, facilitating scenario planning to protect key milestones</li><li>Anticipate and address risks to manufacturing readiness, defining mitigation plans to support rigorous CDMO campaign execution</li><li>Lead recurring and ad-hoc technical forums to drive timely decisions, resolve issues, and capture lessons learned</li><li>Lead continuous improvement initiatives to mature AT-PM ways of working</li><li>Partner with procurement, finance, legal, and internal stakeholders to support CDMO engagement, including RFPs, scope alignment, and contracting coordination</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You take initiative, reliably follow through, and thrive in non-structured environments, navigating ambiguity and changing priorities with a strategic, action-oriented mindset</li><li>You enjoy and excel at problem solving, breaking down complex technical and operational challenges into well-thought-out plans</li><li>You like building structure and scalable frameworks that help cross-functional teams execute efficiently</li><li>You proactively identify risks and roadblocks, communicate tradeoffs, and know when and how to escalate</li><li>You're willing to try, learn, and iterate to keep programs moving forward and partners aligned</li></ul><h3>This role requires:</h3><ul><li>B.Sc. in Biochemistry, Chemical/Biochemical Engineering, or a related field, with 6-8+ years of experience or a MS w/3-6+, including demonstrated ownership of cross-functional deliverables</li><li>A strong customer-service mindset</li><li>Ability to independently facilitate team collaboration, build and maintain integrated plans, and design/improve repeatable business processes</li></ul><p><strong>Preferred / nice-to-haves:</strong></p><ul><li>Experience supporting CMC development and/or technology transfer to CDMOs (e.g., process development, analytics, documentation readiness)</li><li>Experience or knowledge of bioconjugation, gene therapy/AAV, or</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Technology Operations & Platform Reliability]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48997]]></requisitionid>
    <referencenumber><![CDATA[R48997]]></referencenumber>
    <apijobid><![CDATA[r48997]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48997/senior-director-technology-operations-platform-reliability/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are looking for Senior Director, Infrastructure, Operations & App Support to talent to join our Digital and Technology team. In this highly strategic leadership role, you will drive the reliability, scalability, security, and operational excellence of our cloud platforms, AI/ML environments, enterprise applications, and support services. You will lead the evolution of modern cloud operations, Site Reliability Engineering (SRE), IT Service Management (ITSM), Managed Service Provider (MSP) governance, and operational resilience programs while partnering closely with executive leadership to align technology operations with business objectives. This position offers an opportunity to influence enterprise-wide technology strategy and build a high-performing organization focused on innovation, automation, and operational excellence.</p><p><strong>When & where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Own the operational health, availability, performance, and security of enterprise cloud platforms across AWS, Azure, and GCP environments, including AI/ML, data, analytics, and cloud-native application platforms.</p></li><li><p>Establish and mature MLOps and AIOps operational practices including model monitoring, drift detection, automated retraining, inference platform management, and AI workload incident response.</p></li><li><p>Lead enterprise cloud operations modernization through observability, automation, intelligent monitoring, and proactive operational management.</p></li><li><p>Build and lead a mature Site Reliability Engineering (SRE) organization, embedding SLOs, SLIs, error budgets, observability standards, and reliability engineering practices across critical platforms and services.</p></li><li><p>Partner with engineering and architecture teams to implement automation, self-healing capabilities, infrastructure-as-code, and operational efficiency improvements at scale.</p></li><li><p>Govern enterprise on-call frameworks, incident management processes, post-incident reviews, and continuous improvement programs that strengthen service reliability and resiliency.</p></li><li><p>Serve as the executive owner for Managed Service Providers and strategic vendors, overseeing contracts, SLAs, performance metrics, governance frameworks, and executive issues.</p></li><li><p>Lead vendor performance reviews, risk assessments, cost optimization initiatives, and strategic sourcing decisions in partnership with Procurement, Legal, and Finance.</p></li><li><p>Oversee enterprise IT support operations including service desk, Tier 1/2/3 support, and application support functions to ensure best-in-class end-user experiences.</p></li><li><p>Drive adoption and maturity of ITIL-aligned service management practices including Incident, Problem, Change, Release, and Configuration Management.</p></li><li><p>Define and report operational performance metrics including MTTR, MTBF, SLA compliance, first-contact resolution, and customer satisfaction measures.</p></li><li><p>Deliver executive-level reporting to the CIO and senior leadership, translating operational performance and technical risks into actionable business insights.</p></li><li><p>Partner with Security and Compliance teams to maintain cloud security posture, vulnerability management, compliance requirements, and operational risk mitigation initiatives.</p></li><li><p>Lead geographically distributed teams, develop operational leaders, and foster a culture of accountability, inclusion, innovation, and continuous learning.</p></li><li><p>Develop enterprise operational maturity roadmaps across cloud operations, SRE, MSP governance, and support functions while driving continuous improvement and service optimization.</p></li><li><p>Establish and govern disaster recovery and business continuity programs, ensuring resilient and tested recovery capabilities for critical enterprise technologies.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Information Technology, Computer Science, Engineering, or a related discipline; advanced degree preferred.</p></li><li><p>15+ years of progressive experience in enterprise technology operations, infrastructure, cloud platforms, and service delivery leadership.</p></li><li><p>Deep expertise operating large-scale multi-cloud environments across AWS, Azure, and GCP, including cloud governance, architecture patterns, operational tooling, and FinOps optimization.</p></li><li><p>Good experience with AI/ML operational platforms including MLOps, model lifecycle management, monitoring, inference services, and AIOps solutions.</p></li><li><p>Demonstrated success building and leading Site Reliability Engineering organizations and implementing observability frameworks, SLO programs, and incident management capabilities.</p></li><li><p>Strong knowledge of enterprise IT Service Management practices, ITIL v4 frameworks, and ServiceNow or equivalent platforms.</p></li><li><p>Significant experience managing strategic vendor relationships, MSP governance, SLA management, contract oversight, and operational outsourcing models.</p></li><li><p>Understanding of cloud security, vulnerability management, compliance requirements, and operational risk management practices.</p></li><li><p>Experience building, scaling, and developing high-performing global technology organizations, including leaders, managers, and senior technical experts.</p></li><li><p>Experience establishing or significantly expanding capabilities within a Global Capability Center (GCC) environment.</p></li><li><p>Strong strategic thinking, organizational design, and business partnership capabilities with the ability to translate ambiguous challenges into executable technology strategies.</p></li><li><p>Exceptional executive communication, stakeholder management, and cross-cultural leadership skills, with experience engaging senior global leadership teams and board-level stakeholders.</p></li><li><p>Demonstrable ability to operate effectively within a global matrix organization and influence outcomes across diverse stakeholder groups.</p></li><li><p>Passion for continuous improvement, operational excellence, innovation, and developing high-performing teams.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48748]]></requisitionid>
    <referencenumber><![CDATA[R48748]]></referencenumber>
    <apijobid><![CDATA[r48748]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48748/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials, including Phase IV/Real World Evidence studies, from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Experience with Phase IV /RWE preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Health Economics & Outcomes Research (Immunology)]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47988]]></requisitionid>
    <referencenumber><![CDATA[R47988]]></referencenumber>
    <apijobid><![CDATA[r47988]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47988/senior-manager-health-economics-outcomes-research-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Senior Manager will support the execution of our global and regional HEOR strategies and programs, aiming to inform, support and strengthen commercialization activities, including clinical development, marketing, and market access.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>This is located in Sleepy Hollow, NY and is on-site 4 days/week. </p><p><strong>Discover your role:</strong><br>• Partner with cross functional and business partners to develop and support compelling product value propositions with aim to optimize access, reimbursement and uptake.<br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation. These will include: prospective and retrospective observational studies, real world data analyses, registry studies, PRO studies, cost effectiveness and budget impact analyses, modeling studies.<br>• Conduct population and disease state analyses and epidemiology studies to inform clinical development and life-cycle management.<br>• Oversee and guide the development and implementation of Patient Reported Outcomes (PRO) strategies ensuring PRO end points in product labeling and support product differentiation. <br>• Develop and validate PRO endpoints for integration in pivotal studies. <br>• Responsible for including patient-reported outcomes studies into NDA/MAA dossiers and labels, and interacting with Agencies.<br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.<br>• Deliver HEOR presentations to customers to support reimbursement decisions across the portfolio.<br>• Collaborate with Alliance partners on HEOR plans, studies and deliverables; build and maintain constructive and productive relationships . </p><p><strong>This role requires</strong>:<br>• Advanced graduate degree (PhD, MS, or PharmD) in HEOR-related field (e.g. health economics, epidemiology, healthcare/data analytics, health services research, public health) with at least 2 year post-graduate experience.<br>• For PharmD, a 3+ years fellowship training, pharma or consulting experience in health economics and outcomes research is required; For MS, at least 3 years experience is required.<br>• Strong technical expertise required in design and conduct of HEOR studies and models;<br>• Excellent written and verbal communication skills required.<br>• Ability to interact with and present to Senior Management.<br>• Experience in immunology therapeutic areas a plus.<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Production AI/ML Engineering, Advanced Informatics]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48875]]></requisitionid>
    <referencenumber><![CDATA[R48875]]></referencenumber>
    <apijobid><![CDATA[r48875]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48875/associate-manager-production-aiml-engineering-advanced-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, Production AI/ML Engineering to join our Advanced Informatics team. In this role, you will architect and scale the computational ecosystem that powers our AI/ML applications — transforming population-scale clinical and claims data into reliable, production-grade model inference — while collaborating closely with Applied AI managers, clinical informaticists, and data governance partners. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Tarrytown or Armonk, NY or Warren, NJ</p><p><strong>Discover your role:</strong><br>• Architect and maintain a scalable AWS/Kubernetes ecosystem supporting model training, batch inference, and real-time serving<br>• Design and maintain production-grade ML pipelines over population-scale clinical and claims data, including ingestion, normalization, and transformation across controlled terminologies (SNOMED CT, ICD-10/11, LOINC, RxNorm, OMOP CDM).<br>• Develop RESTful APIs that reliably expose model inference to downstream teams and applications<br>• Operationalize models from the Applied AI team — owning deployment, versioning, rollback, and A/B testing<br>• Build MLOps infrastructure (CI/CD, feature stores, model registries) and champion engineering best practices<br>• Own monitoring, alerting, and incident response for production ML systems<br>• Partner with data governance and compliance to ensure pipelines and deployments adhere to data use agreements and de-identification standards.<br>• Shape capacity planning and the long-term technical roadmap for the team's AI/ML platform</p><p><strong>This role requires:</strong><br>• Bachelor's degree in Computer Science, Software Engineering, Data Science, Biomedical Informatics, or related (Master's preferred) with 7–9 years of progressive ML/platform/software engineering experience with an infrastructure focus<br>• Proven experience designing and operating ML infrastructure at enterprise scale on AWS (SageMaker, ECS, EC2, S3, Lambda, or equivalent).<br>• Strong Kubernetes expertise: cluster management, workload scheduling, autoscaling, and deploying containerized ML services in production.<br>• Proficiency building and maintaining RESTful APIs; experience with API design, versioning, performance tuning, and integration with ML serving frameworks.<br>• Hands-on experience with Postgres: schema design, query optimization, and integration into data and ML pipelines.<br>• Expert-level Python and SQL; strong software engineering fundamentals including Git, modular design, testing, and CI/CD.<br>• Proficiency with MLOps tooling: experiment tracking (MLflow, W&B), model registries, containerization (Docker), and pipeline orchestration (Airflow, Prefect, or similar).<br>• Informatics knowledge with health or life sciences data — EHR/EMR records, claims data, clinical notes, or administrative data is preferred. </p><p>#AAI<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Manufacturing Technical Services]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49659]]></requisitionid>
    <referencenumber><![CDATA[R49659]]></referencenumber>
    <apijobid><![CDATA[r49659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49659/senior-director-manufacturing-technical-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Manufacturing Technical Services (MTS) to join our team, supporting our fill/finish clinical and commercial drug product manufacturing operations. In this role, you will provide technical leadership across equipment characterization, cycle development, tech transfer, and troubleshooting for our aseptic fill/finish value stream, while collaborating with Quality, Engineering, Automation, and Validation to keep our fill/finish equipment and processes in a state of control.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Monday- Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads technical characterization, cycle development, and troubleshooting for aseptic fill/finish equipment, including filling systems, isolators, stoppering, capping, visual inspection, device assembly, labeling, and packaging</p></li><li><p>Directs tech transfer activities, including clinical and new product introductions, site-to-site transfers, and scale-up/scale-down</p></li><li><p>Owns the visual inspection program, spanning manual inspector qualification/AQL and automated inspection (AVI) systems, including defect library development and camera/algorithm optimization</p></li><li><p>Oversees alarm management and process monitoring strategy, including PAT, continuous monitoring, and alarm rationalization</p></li><li><p>Serves as a key technical resource during regulatory inspections and health authority interactions, authoring and defending technical justifications</p></li><li><p>Owns CAPA and root cause investigations for deviations and complaints tied to fill/finish equipment or process</p></li><li><p>Builds and develops a multi-faceted technical team, growing the maturity of the MTS function over time</p></li><li><p>Communicates technical and equipment risk clearly to senior leadership, translating it into executable steps for manufacturing operations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Director Level: Bachelor's or advanced degree in Engineering, Life Sciences, or a related technical field and 10+ years of biopharmaceutical manufacturing experience, including 5+ years in aseptic fill/finish or equivalent combination or education and experience</p></li><li><p>Senior Director Level: Bachelor's or advanced degree in Engineering, Life Sciences, or a related technical field and 15+ years of biopharmaceutical manufacturing experience, including 8+ years in aseptic fill/finish or equivalent combination or education and experience</p></li><li><p>Deep expertise in aseptic fill/finish equipment characterization and troubleshooting for commercial and clinical manufacturing lines</p></li><li><p>Strong regulatory and quality acumen, with the ability to support inspections and defend technical positions to health authorities</p></li><li><p>Platform experience with Bausch+Ströbel (VarioSys, CombiSys), Seidenader Inspection, Harro Hofliger assembly, or Körber (Dividella/Pester) packaging preferred</p></li><li><p> Automation/data historian familiarity (PAS-X, FactoryTalk, PI Vision) preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Compliance Specialist (Quality Risk Management)]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49485]]></requisitionid>
    <referencenumber><![CDATA[R49485]]></referencenumber>
    <apijobid><![CDATA[r49485]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49485/quality-compliance-specialist-quality-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill a Quality Compliance Specialist (Quality Risk Management) position. This position is responsible for supporting Regeneron’s Internal Drug Product Manufacturing operations through the use of quality risk management (QRM). Job functions will primarily consist of the broad application of patient centered QRM across a full spectrum of processes vital to the operations. Specifically, the active facilitation of quality risk assessments, risk reviews and other quality risk-based programs supporting the Quality System (e.g., change control, deviation management, etc.). The person in this role will be consistently challenged with assignments, touching almost every phase of our process.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work schedule: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing technical expertise in quality risk management to a broad base of customers throughout the organization, including Quality Assurance, Quality Control, Manufacturing, Medical Device and Facilities</p></li><li><p>Facilitating data driven risk assessments and risk reviews using appropriate methodologies (e.g., FMEA, RBIA, REM and HACCP)</p></li><li><p>Partnering with Risk Assessment Owners to define scope, acceptance criteria, and evaluation scales</p></li><li><p>Guiding teams through risk identification, analysis, control/mitigation, and residual risk evaluation</p></li><li><p>Preparing and revising QRM documents</p></li><li><p>Developing and improving the quality risk management program</p></li><li><p>Contributing to contamination control strategy (CCS) and aseptic processing risk assessments for fill/finish operations; interface with EM, utilities, and equipment owners.</p></li><li><p>Preparing for and supporting regulatory, customer, and internal audits/inspections</p></li><li><p>Coaching colleagues on QRM principles and driving consistency in application</p></li><li><p>Tracking metrics (e.g., on-time risk reviews, cycle time) and identifying opportunities for continuous improvement.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Biological Sciences, Chemistry, Biochemistry, Engineering or related field, or equivalent combination of education and experience, and the following amount of relevant work experience for each level:</p><ul><li><p>Specialist - 2+ years</p></li><li><p>Senior Specialist - 5+ years</p></li><li><p>Level will be determined based on experience</p></li></ul></li></ul><ul><li><p>Excellent collaboration, influence, and communication skills</p></li><li><p>Proficiency at facilitating cross-functional discussions</p></li><li><p>Proficient digital literacy in Microsoft (MS) Word, Excel and PowerPoint required. Experience with Veeva heavily preferred.</p></li><li><p>Having an understanding of QRM principles</p></li><li><p>Ability to interpret complex technical and systems information and make sound risk-based decisions</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - PITTSBURGH, PA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48946]]></requisitionid>
    <referencenumber><![CDATA[R48946]]></referencenumber>
    <apijobid><![CDATA[r48946]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48946/medical-account-specialist-ii-hematology-pittsburgh-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Pittsburgh]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: Pittsburg, PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - LOUISIANA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49216]]></requisitionid>
    <referencenumber><![CDATA[R49216]]></referencenumber>
    <apijobid><![CDATA[r49216]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49216/medical-account-specialist-ii-hematology-louisiana/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Louisiana]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: New Orleans, LA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45310]]></requisitionid>
    <referencenumber><![CDATA[R45310]]></referencenumber>
    <apijobid><![CDATA[r45310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45310/medical-director-clinical-development-oncology-lung-breast-colorectal-gastric-cancers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Oncology team, supporting solid tumor drug development on-site in Tarrytown, NY or Warren, NJ. In this role, you will design clinical study concepts, oversee the medical and scientific integrity of clinical trials, and ensure patient safety across trial activities while collaborating with the Global Clinical Study Team and key investigators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><p><strong>Location:</strong> Tarrytown, NY</p></li><li><p><strong>Travel: </strong>10% to relevant conferences</p></li></ul><br><h3>Discover your role:</h3><ul><li><p>Define clinical trial-related goals and objectives</p></li><li><p>Conduct literature and database research to inform trial design</p></li><li><p>Ensure the scientific accuracy of clinical study concepts through rigorous review and consultation with internal and external experts</p></li><li><p>Oversee the medical content of clinical study reports and the analysis of clinical data, including safety monitoring</p></li><li><p>Safeguard patient safety across all trial activities and procedures</p></li><li><p>Lead and supervise the Global Clinical Study Team to deliver high-quality program milestones on schedule</p></li><li><p>Build and maintain relationships with key study investigators</p></li></ul><br><h3>This role requires:</h3><ul><li><p>MD or MD/PhD degree or the equivalent</p></li><li><p>Oncology clinical fellowship training strongly preferred</p></li><li><p>At least 2 years of translational and/or clinical research experience in academia or industry</p></li></ul><p>#MDJobs, #MDJobsCD, #GDTherapeuticJobs, #Oncology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs, Allergy & Respiratory (Asthma, COPD)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46160]]></requisitionid>
    <referencenumber><![CDATA[R46160]]></referencenumber>
    <apijobid><![CDATA[r46160]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46160/medical-director-medical-affairs-allergy-respiratory-asthma-copd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Medical Affairs to join our Allergy & Respiratory team, supporting Regeneron's strategic assets in asthma and/or COPD. In this role, you will drive the development and execution of medical strategies, ensuring scientific integrity and accuracy, while collaborating with field medical teams, medical operations, HEOR, publication management, and external clinical experts.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Sleepy Hollow, NY or Warren, NJ</li><li><strong>Travel: </strong>25% to relevant conferences/congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Develop and oversee US and ex-US medical strategy, including scientific communications, publications, and field collaborations</li><li>Support the design, conduct, oversight, analysis, and reporting of post-approval respiratory clinical trials</li><li>Partner with CRO medical monitors and participate in clinical study team meetings and data review sessions</li><li>Drive generation and dissemination of clinical and non-clinical data supporting the medical strategy</li><li>Collaborate across a multifunctional, matrix organization spanning medical, operations, and statistics teams</li><li>Cultivate long-term strategic partnerships with clinical experts, societies, and advocacy groups</li><li>Support commercial activities, including promotional material review and speaker/colleague training</li></ul><br><h3>This role requires:</h3><ul><li>MD/MBBS or equivalent medical degree, with specialized training and experience in pulmonology or allergy, specifically asthma</li><li>At least 2-4 years of industry experience in Allergy/Respiratory Medical Affairs and/or Clinical Development</li><li>Demonstrated experience in clinical trial execution</li><li>Strong presentation and communication skills, with the ability to deliver succinct, strategic insights to senior management</li><li>Experience working in an alliance setting strongly preferred</li></ul><p>#MDJobs, #MDJOBSMA, #GDMAJobs, #Respiratory, #Asthma, #COPD</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - ATLANTA North, GA]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48026]]></requisitionid>
    <referencenumber><![CDATA[R48026]]></referencenumber>
    <apijobid><![CDATA[r48026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48026/medical-account-specialist-ii-neurology-atlanta-north-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Atlanta]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Atlanta North (Metro), GA</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Supply Planning and Reporting Analyst, Advanced Therapies]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48755]]></requisitionid>
    <referencenumber><![CDATA[R48755]]></referencenumber>
    <apijobid><![CDATA[r48755]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48755/principal-supply-planning-and-reporting-analyst-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Supply Planning Analyst (Senior or Principal) to join our Integrated Operations (IOPS) team, supporting Commercial and Clinical programs in a cross-functional environment. In this role, you will own end-to-end supply planning across advanced therapy modalities — including siRNA, AAV-based gene therapies, LNP platforms, and CRISPR-based medicines — while collaborating with Manufacturing, Quality, Regulatory, Clinical Operations, and Commercial teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><br><strong>When & where:</strong></p><ul><li>Location: Troy, New York</li><li>Work model: Monday – Friday 8am – 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead end-to-end supply planning for assigned Clinical and Commercial programs, ensuring uninterrupted supply across advanced therapy modalities</li><li>Execute master production scheduling (MPS), material requirements planning (MRP), demand management, and inventory management for assigned programs and sites</li><li>Build and maintain inventory reports accounting for complex manufacturing requirements, shelf-life constraints, and cold-chain considerations</li><li>Design and implement statistical models, simulations, and algorithms to forecast and quantify operational and supply chain performance metrics</li><li>Generate dashboards, data visualizations, and advanced Excel tools that communicate analytical insights and drive informed planning decisions</li><li>Support Sales, Inventory & Operations Planning (SIOP) processes by consolidating data and facilitating information flow across demand, supply, and integration functions</li><li>Partner with cross-functional teams to ensure compliant, disciplined planning in alignment with GMP requirements and audit readiness standards</li><li>Execute advanced proficiency in Microsoft Excel, including the ability to design complex planning tools and models with strong working knowledge of MPS, MRP, demand management, and inventory management principles</li><li>Previous experience in pharmaceutical, biotechnology, or advanced therapy manufacturing and familiarity with regulatory and supply chain considerations specific to advanced therapy modalities (siRNA, AAV, LNP, CRISPR) is preferred</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Business, Supply Chain Management, or a Science discipline</li><li>Senior Analyst: 5+ years of supply chain experience</li><li>Principal Analyst: 8+ years of supply chain experience</li><li>Master's degree (MBA, MS Supply Chain, or life sciences) and/or APICS certification (CPIM, CSCP) or Lean/Six Sigma knowledge is a plus</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Obesity]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46851]]></requisitionid>
    <referencenumber><![CDATA[R46851]]></referencenumber>
    <apijobid><![CDATA[r46851]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46851/medical-director-clinical-development-obesity/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Obesity team supporting our Clinical Development Unit in the area of metabolism for obesity or Type 2 diabetes. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Travel: 10% to relevant conferences</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>You guide the Global Clinical Study Team to deliver high-quality trials on time.</p></li></ul><ul><li><p>You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance</p></li><li><p>You lead clinical study and protocol development and present to internal and external stakeholders.</p></li><li><p>You provide clinical and scientific leadership for data review, study reports, and publications.</p></li><li><p>You work closely with cross-functional partners to advance program goals and key deliverables.</p></li><li><p>You collaborate with discovery teams to help shape future targets and development opportunities in the field.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable.</p></li><li><p>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</p></li><li><p>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</p></li></ul><p>#MDJobsCD, #MDJobs, #GDTherapeuticJobs, #Obesity</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Rhinology *Kanagawa Area]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49579]]></requisitionid>
    <referencenumber><![CDATA[R49579]]></referencenumber>
    <apijobid><![CDATA[r49579]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49579/medical-representative-mr-rhinology-starkanagawa-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative Immunology Commercial Japan Region to join our Immunology Commercial Team, supporting our Japan business in a hybrid work model. In this role, you will achieve immunology sales objectives while collaborating with alliance partners and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Kanagawa, Japan</p><p>Work model: Field</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Achieve immunology sales objectives through territory budget and expense management.</li><li>Develop annual territory business plans using market insights and brand strategies.</li><li>Use key data sources to build territory action plans.</li><li>Deliver customer value through strategic engagement and tailored solutions.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Operate within regulatory, legal, and compliance requirements.</li><li>Collaborate with alliance partners to deliver shared business objectives.</li><li>You build strong customer relationships while managing priorities effectively.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree or equivalent experience.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>MR Certification and a valid driver license.</li><li>Strong customer engagement skills with a value-focused approach.</li><li>Ability to conduct disease and concept-based selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and independent execution skills.</li><li>Computer proficiency with word processing, spreadsheets, databases, and email software.</li><li>Ability to tailor presentations to different audiences.</li><li>Alliance experience or exposure.</li><li>Therapy area knowledge in rhinology and respiratory preferred.</li><li>Biologics sales experience preferred.</li><li>Current clinical knowledge of therapy areas and competitor brands preferred.</li><li>Established key opinion leader relationships in rhinology and respiratory preferred.</li><li>English fluency is a plus.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Facilities Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47620]]></requisitionid>
    <referencenumber><![CDATA[R47620]]></referencenumber>
    <apijobid><![CDATA[r47620]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47620/facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><br><p><strong>What you’ll do:</strong></p><ul><li><p>Building and specifying cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</p></li><li><p>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</p></li><li><p>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</p></li><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li><li><p>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</p></li><li><p>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</p></li><li><p>Implementing corrective/preventative actions for existing equipment and maintenance processes</p></li><li><p>Preparing engineering evaluations and test plans for and executing modification change control documentation</p></li><li><p>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</p></li><li><p>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have strong analytical and interpersonal skills</p></li><li><p>You are able to prioritise and re-prioritise as needed and adapt to change</p></li><li><p>You are comfortable working in a fast-paced setting</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>To be considered for this position you should have a BS/BA in Mechanical Engineering or equivalent, with 5 years of relevant experience preferably in the Pharma/Biotech industry.</p></li><li><p>Senior Engineer: BS/BA in Mechanical Engineering with 5 years' minimum experience</p></li><li><p>Engineer: BS/BA in Mechanical Engineering with 2 years' minimum experience</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLTO</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp EHS specialist]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48472]]></requisitionid>
    <referencenumber><![CDATA[R48472]]></referencenumber>
    <apijobid><![CDATA[r48472]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48472/temp-ehs-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Temporary Environmental, Health and Safety Specialist to join our <strong>Environmental, Health and Safety </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Developing, implementing and monitoring environmental, health & safety programs to ensure compliance with all applicable government regulations and company standards and values</p></li><li><p>Establishing, maintaining and auditing the Environmental and Health & Safety Management System</p></li><li><p>Determining and addressing site EHS issues and employee concerns</p></li><li><p>Performing incident management activities including injury management investigations and associated recordkeeping</p></li><li><p>Identifying, implementing and tracking corrective actions to prevent recurrence</p></li><li><p>Performing Environmental, Health and Safety risk assessments and makes recommendations to control hazards</p></li><li><p>Creating, implementing and maintaining Environmental, Health and Safety training program for health, safety and the environment</p></li><li><p>Responsible for developing appropriate emergency plans and response capabilities</p></li><li><p>Staying abreast of new Environmental, Health and Safety government regulations as they are promulgated as well as new developments in industry (best practices)</p></li><li><p>Building relationships with key departments to foster support for Environmental, Health and Safety programs</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>A thorough knowledge of Environmental, Health and Safety legislation for a pharmaceutical facility operating within Ireland/Europe</p></li><li><p>Knowledge of behavioural based safety programs</p></li><li><p>Operational Safety Experience: Safe Systems of Work - Environmental, Health and Safety permitting, Fatality Prevention Programme - EHS Control of Hazardous Energy – Lock Out Tag Out</p></li><li><p>The ability to lead and direct others and work as part of a team</p></li><li><p>Logical problem solving skills</p></li><li><p>Excellent interpersonal and communication skills coupled with good ability to produce technical reports</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>For this opportunity you should have a BS/ BA in Health and Safety or related field with 5+ years of experience working in an Environmental, Health and Safety role within the pharmaceutical industry or similar industry.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Enterprise Data]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49700]]></requisitionid>
    <referencenumber><![CDATA[R49700]]></referencenumber>
    <apijobid><![CDATA[r49700]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49700/executive-director-enterprise-data/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're looking for an Executive Director of Enterprise Data to join our fast-moving Enterprise Data & AI organization. You'll be responsible for the integrity, accessibility, and governance of our enterprise data assets, making sure our proprietary scientific and clinical data is structured, governed, and ready for AI at scale. You'll build foundational data capabilities, from quality standards to the semantic layer that keeps definitions consistent across the company. This role reports to the VP, Enterprise Data & Information Management, and offers the chance to turn Regeneron's data into one of its biggest AI advantages.</p><br><h3><strong>When & where:</strong></h3><ul><li><strong>Location:</strong> This role is open to any of our Tri-State locations: Sleepy Hollow, NY, Tarrytown, NY, Armonk, NY, Warren, NJ or Cambridge, MA</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Enforce enterprise data quality standards, turning policy into day-to-day operating procedures</li><li>Lead master data management and data cataloging, keeping data assets inventoried and accessible</li><li>Own and run the enterprise semantic layer, keeping data definitions consistent across functions and AI systems</li><li>Build and maintain the enterprise business glossary and taxonomy</li><li>Lead development of knowledge graph infrastructure that supports advanced AI and scientific work</li><li>Design and deliver a federated, AI-ready data ecosystem across domains</li><li>Maintain GxP-compliant data standards, keeping regulated pipelines audit-ready</li><li>Own data privacy and security standards across the enterprise data estate</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have built data foundations that enable AI and analytics at enterprise scale</li><li>Bring deep, hands-on experience with data governance, master data management, and metadata management</li><li>Can operate as both strategist and technical leader in federated data architecture and semantic layers</li><li>Understand how data governance intersects with regulatory, clinical, and commercial requirements</li><li>Stay current on the AI data landscape, including vector databases, knowledge graphs, and RAG</li><li>Have experience partnering with distributed engineering teams, including global delivery models</li><li>Communicate and build influence across technology, business, science, legal, and regulatory teams</li><li>Enjoy developing data engineering and governance talent across disciplines</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>A Bachelor's degree in a related field (advanced degree required for certain scientific or clinical positions)</li><li>17+ years of experience in enterprise data management, data governance, or data architecture</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr IT Auditor]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49837]]></requisitionid>
    <referencenumber><![CDATA[R49837]]></referencenumber>
    <apijobid><![CDATA[r49837]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49837/sr-it-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior IT Internal Audit Compliance & Technology Risk Specialist to join our Internal Audit team, supporting our SOX 404 compliance and IT audit programs in a hybrid work environment. In this role, you will contribute to the execution of IT compliance reviews, continuous auditing analytics, and operational audits while collaborating with accounting, technology, operational teams, and Internal Audit colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Review IT processes and controls within scope of the company's SOX 404 program and assess control effectiveness.</p></li><li><p>Develop and implement continuous auditing analytics to identify weaknesses in compliance-related exposures, operational processes, and internal controls.</p></li><li><p>Partner with Internal Audit colleagues to develop risk-based audit programs and support departmental deliverables.</p></li><li><p>Contribute to IT operational audits in accordance with Institute of Internal Auditors (IIA) standards, internal policies, and procedures.</p></li><li><p>Implement assigned audit sections independently with minimal supervision while maintaining audit quality and compliance.</p></li><li><p>Complete SOX 404 IT compliance reviews and testing of controls assigned by Internal Audit management.</p></li><li><p>Provide internal control expertise to business functions and departments seeking guidance on governance and control practices.</p></li><li><p>Find opportunities to enhance operational efficiencies and support the preparation of audit recommendations and reports for Senior Management and the Audit Committee.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Minimum 3 years of progressive experience in IT audit, information security, or technology risk.</p></li><li><p>Experience auditing and evaluating IT infrastructure, cybersecurity risks and controls, and operating systems.</p></li><li><p>Strong understanding of SOX, Committee of Sponsoring Organizations (COSO), Control Objectives for Information and Related Technologies (COBIT), National Institute of Standards and Technology (NIST), Good Practice (GxP), General Data Protection Regulation (GDPR), and related governance and regulatory frameworks.</p></li><li><p>Knowledge of IT compliance programs, process reviews, testing of controls, and internal control frameworks.</p></li><li><p>Experience using data analytics tools such as Dataiku, Alteryx, or similar technologies.</p></li><li><p>Understanding of artificial intelligence concepts, associated risks including model governance, data quality, access, ethical use, and controls relevant to AI-enabled processes.</p></li><li><p>Ability to interact autonomously with middle management and provide practical guidance on risk, governance, and control matters.</p></li><li><p>Certified Information Systems Auditor (CISA), Certified Information Security Manager (CISM), and/or Certified Information Systems Security Professional (CISSP) preferred.</p></li><li><p>Pharmaceutical, life sciences, or other regulated industry experience preferred.</p></li><li><p>Big Four or public accounting experience preferred.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Global Procurement]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44844]]></requisitionid>
    <referencenumber><![CDATA[R44844]]></referencenumber>
    <apijobid><![CDATA[r44844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44844/manager-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager Global Procurement International Markets Japan to join our Global Procurement team, supporting our Japan market in a hybrid work model. In this role, you will deliver procurement activities and sourcing priorities for Japan while collaborating with collaborators, country leads, and category teams. This position offers the opportunity to supply to a fast-growing, science-driven organization making a relevant difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Tokyo, Japan</p><p>Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Partner with collaborators and Global Procurement to deliver local execution of global priorities.</li><li>Implement global category strategies across sourcing, contracting, and supplier relationship management.</li><li>Provide Japan market input to strengthen global category strategies.</li><li>Review contracts and monitor country spend trends using data insights.</li><li>Partner with collaborators to understand strategy, budgets, and future requirements.</li><li>Lead sourcing, negotiation, and contracting activities supporting business needs.</li><li>Drive value through cost savings, cash flow improvement, and procurement efficiencies.</li><li>You thrive in a changing environment and help drive continuous improvement.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in a relevant field.</li><li>5+ years of indirect procurement experience.</li><li>Dynamic procurement experience, preferably within Pharma or Biopharma.</li><li>Experience across Commercial, Corporate/Indirect, and Research & Development categories preferred.</li><li>Experience leading or supporting global category teams, processes, and suppliers.</li><li>Expertise in sourcing, negotiations, contracting, and supplier relationship management.</li><li>Knowledge of supply market evaluation, risk, compliance, and financial assessment tools.</li><li>Ability to build influential collaborator and supplier relationships.</li><li>Knowledge of rates, unit costs, costing structures, and supply market dynamics.</li><li>Working knowledge of sourcing, contracting, Enterprise Resource Planning systems, and eRFx platforms preferred, including Oracle, Zycus, GEP, or Ariba.</li><li>Proficiency with Word, Excel, and PowerPoint.</li><li>Ability to use data and market intelligence to support decision-making.</li><li>Ability to operate with integrity, focus, and clarity in ambiguous environments.</li><li>Collaboration and cross-functional partnership skills.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology-Bronx, NY]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49767]]></requisitionid>
    <referencenumber><![CDATA[R49767]]></referencenumber>
    <apijobid><![CDATA[r49767]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49767/medical-specialist-i-dermatology-bronx-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Bronx, NY</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus</p></li><li><p>The successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience</p></li><li><p>A minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred</p></li><li><p>This role requires the ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46894]]></requisitionid>
    <referencenumber><![CDATA[R46894]]></referencenumber>
    <apijobid><![CDATA[r46894]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46894/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>We are seeking a Senior Project Engineer who will be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment. This position will provide engineering support and problem solving support for existing equipment and manufacturing processes.</p></div><div><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Designing and specifying cGMP process equipment, piping, and controls</p></li><li><p>Managing small-to-mid-sized projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance, and installation of equipment</p></li><li><p>Preparing piping and instrumentation diagrams (P&IDs) and other related drawings</p></li><li><p>Developing Process Flow Diagrams (PFDs) for manufacturing processes</p></li><li><p>Supporting the QA Validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Reviewing and approving lifecycle documentation, cleaning validation protocols, and summary reports</p></li><li><p>Assisting with investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</p></li><li><p>Assisting management with tracking of department throughput and efficiency</p></li><li><p>Representing the engineering department at cross-functional meetings</p></li><li><p>Supervising direct reports as needed</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations and test plans, and executing change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors as needed</p></li><li><p>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p></li><li><p>Maintaining company reputation by ensuring compliance with all relevant laws, policies, and regulations</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have excellent technical and analytical skills.</p></li><li><p>You are skilled at problem-solving and continuous improvement.</p></li><li><p>You possess strong communication and collaboration skills.</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>To be considered for this opportunity you should have a BS/BEng or higher in chemical/process/mechanical engineering with 5+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#LI-Onsite #JOBSIEPR #IRELIM #REGNIRLTO</strong></p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Assistant General Counsel, Privacy]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46433]]></requisitionid>
    <referencenumber><![CDATA[R46433]]></referencenumber>
    <apijobid><![CDATA[r46433]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46433/senior-director-assistant-general-counsel-privacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As a key member of the Privacy Office in Regeneron’s Law Department, this role will enable our rapidly growing and globally expanding business to develop and execute innovative data-driven strategies in accordance with data privacy, cybersecurity and AI laws. This role will serve as the Privacy Office's primary legal<strong> </strong> support for our Digital & Technology function and other business areas as may be needed. This role will report to Regeneron’s Chief Privacy Officer.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY, Cambridge, MA</p></li><li><p>Work model/flexibility: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Shaping the legal framework for Regeneron's cyber risk strategy and counseling senior management on cyber-related legal obligations in the U.S. and globally.</p></li><li><p>Leading the Privacy Office's incident response function, including counseling stakeholders to prepare for and respond to complex cyber and privacy incidents, and directing the privacy professionals responsible for incident intake, tracking, and investigations.</p></li><li><p>Set strategy and direction for assessing potential privacy risks associated with innovative new initiatives and driving the development of appropriate controls, training and guidance to enable compliance with applicable regulations.</p></li><li><p>Engagement in support of Regeneron's evolving AI governance framework including participating in use case assessments and counseling to manage associated privacy risk.</p></li><li><p>Drive the development of privacy policies, procedures and guidance that enable consistent, scalable and globally aligned practices. Collaborate with Law Department colleagues, Digital & Technology and business functions in development of related AI, cybersecurity and data governance policies and standards.</p></li><li><p>Anticipating and evaluating developments in global data privacy together with related cybersecurity and AI laws (including related legislation and industry practices), and translating those insights into governance strategies and practical business guidance.</p></li><li><p>Determining approach to operationalizing compliance with regional and local laws; advising on the application and solutions for complying with biometric and other emerging data-related laws.</p></li><li><p>Representing the Privacy Office as a member of Regeneron's technology-related committees and working groups.</p></li><li><p>Partnering with Privacy Office colleagues to contribute to the implementation and advancement of the Regeneron Privacy Program.</p></li><li><p>Collaborating with our Government Affairs division on opportunities to influence legislation and regulatory policy</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A JD and be licensed to practice law in New York State or eligible for licensure as a registered in-house counsel.</p></li><li><p>At least 15 years of legal experience at a law firm and/or in-house, with at least 10 years of experience of directly relevant experience. Biotechnology, pharmaceutical or related life science experience strongly preferred.</p></li><li><p>Strong knowledge of local and global privacy, cybersecurity and AI laws and familiarity with associated risk management frameworks and standards (e.g., NIST).</p></li><li><p>Exceptional oral, written, and presentation communication skills, with the ability to effectively communicate and translate complex legal analysis into practical guidance for a varied audience.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Commercial Insights and Analytics, Immunology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49946]]></requisitionid>
    <referencenumber><![CDATA[R49946]]></referencenumber>
    <apijobid><![CDATA[r49946]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49946/associate-director-commercial-insights-and-analytics-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are seeking an Associate Director, Commercial Insights & Analytics - Immunology to join our Commercial Insights & Analytics organization. Reporting directly to the Director, Commercial I&A, this role will lead the India-based Immunology I&A team and serve as a strategic partner to global stakeholders. The successful candidate will drive analytics, insights generation, business performance evaluation, and decision support activities across the Immunology Commercial Business Unit.</p><p>This position offers the opportunity to influence commercial strategy through data-driven insights, lead high-performing teams, and collaborate with cross-functional partners across global markets to enhance business performance and patient impact.<br> </p><p><strong>When & where:</strong></p><p><strong>Hyderabad, India (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li>Lead the India-based Commercial I&A Immunology team and develop a high-performance, collaborative culture.</li><li>Drive innovation, standard processes, and collaboration as part of the Global Capabilities Center (GCC) I&A leadership team.</li><li>Develop team capabilities through coaching, mentoring, and leadership development initiatives.</li><li>Serve as the primary point of contact for Global, U.S., and International Immunology leadership teams.</li><li>Actively participate in the Commercial Immunology I&A Steering Committee and oversee committee priorities, actions, and communications.</li><li>Partner with advanced analytics teams to demonstrate predictive models, segmentation strategies, and targeting approaches.</li><li>Oversee analytics pods delivering actionable insights across multiple brands and markets.</li><li>Guide the development of executive-ready presentations that communicate trends, business implications, and strategic recommendations.</li><li>Lead assessment of brand and market performance by integrating sales, claims, market research, and competitive intelligence data.</li><li>Conduct hypothesis-driven analyses to address key business questions and identify performance drivers.</li><li>Design and enhance performance measurement frameworks, KPIs, and executive dashboards.</li><li>Identify data gaps and collaborate with data management teams to strengthen data infrastructure.</li><li>Assess and implement innovative analytical methodologies that improve market understanding and brand differentiation.</li><li>Incorporate competitive intelligence and primary market research findings into strategic business recommendations.</li><li>Provide strategic oversight and problem-solving support across the Commercial I&A Immunology team.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Business, Life Sciences, Analytics, Statistics, Economics, Engineering, or a related field.</li><li>10+ years of experience in the pharmaceutical or biotechnology industry within commercial analytics, consulting, insights, or related functions.</li><li>Demonstrated experience leading and developing small to large teams.</li><li>Experience supporting brand strategy, forecasting, and commercial decision-making through analytics and insights.</li></ul><ul><li>Advanced SQL and data analytics skills.</li><li>Experience accessing and analyzing data across multiple platforms and sources.</li><li>Proficiency with business intelligence and visualization tools such as Power BI, Tableau, or similar platforms.</li><li>Experience with Snowflake preferred.</li><li>Strong experience working with commercial pharmaceutical datasets, including sales, claims, distribution, and media data.</li><li>Experience developing KPIs, dashboards, and performance measurement frameworks.</li></ul><ul><li>Strong expertise in pharmaceutical/biotech Insights & Analytics, brand performance measurement, and decision support.</li><li>Proven ability to influence business strategy through data-driven recommendations.</li><li>Strong storytelling skills with experience creating executive-level presentations.</li><li>Experience conducting ad-hoc analyses and addressing ambiguous business challenges.</li><li>Strong understanding of primary market research methodologies and forecasting approaches.</li><li>Excellent analytical, problem-solving, and critical-thinking capabilities.</li><li>Ability to work effectively across functions and global stakeholder groups.</li><li>Strong verbal and written communication skills with the ability to engage all levels of the organization.</li><li>Experience operating within cross-functional delivery models and matrix organizations.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45490]]></requisitionid>
    <referencenumber><![CDATA[R45490]]></referencenumber>
    <apijobid><![CDATA[r45490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45490/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager </strong>to join our<strong> Regulatory Affairs Advertising and Promotion</strong> team. In this role, you will apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Trade Compliance Analyst, Customs Brokerage]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46522]]></requisitionid>
    <referencenumber><![CDATA[R46522]]></referencenumber>
    <apijobid><![CDATA[r46522]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46522/senior-trade-compliance-analyst-customs-brokerage/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Trade Compliance Analyst, Customs Brokerage to join our IOPS team, supporting import and export operations across Regeneron's global supply chain. In this role, you will execute daily trade compliance activities — including product classification, licensing, permits, and customs coordination — while serving as a key liaison between internal stakeholders, customs brokers, and regulatory agencies. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li><li>Travel percentage: ~5%</li></ul><p><strong>Discover your role:</strong></p><ul><li>Serve as the primary point of contact for all tactical trade compliance functions, including daily coordination with Regeneron's customs brokers for import and export activities</li><li>Review, validate, and confirm US Harmonized Tariff System (HTS) and Export Commodity Control (ECCN) classifications for formulated drug substance products and raw materials</li><li>Act as business liaison for Customs (CBP), FDA, and USDA, including issue resolution and keeping the business current on regulatory changes and trade compliance best practices</li><li>Manage and update Export and Import Trade Compliance Manuals; create and maintain trade compliance SOPs as needed</li><li>Research, prepare, and submit applications for export and import licenses and permits, conducting classification research to verify requirements</li><li>Partner cross-functionally with internal teams, vendors, and brokerage partners to ensure compliant and efficient trade operations</li><li>Deliver periodic trade compliance training to internal business stakeholders</li><li>Navigate complex pharmaceutical classification procedures with accuracy and sound judgment in a fast-paced, high-interaction environment</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in a related field</li><li>Trade Compliance Analyst: 2+ years of experience</li><li>Senior Trade Compliance Analyst: 5+ years of experience</li><li>May consider equivalent combination of education and experience; level determined based on qualifications</li><li>Experience in customs brokerage or trade compliance with an importer/exporter in a chemical and/or FDA-regulated industry, Licensed Customs Broker preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Business Office]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47016]]></requisitionid>
    <referencenumber><![CDATA[R47016]]></referencenumber>
    <apijobid><![CDATA[r47016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47016/director-global-patient-safety-business-office/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global</strong> <strong>Patient Safety</strong> team.</p><p>The Director, GPS Business Office, serves as a strategic partner to the SVP of Global Patient Safety, driving execution of GPS’ overarching strategic plan, including the annual department operating plan, long-term roadmap, and key transformation initiatives for pharmacovigilance (PV) enablement (e.g., Global Capabilities Center (GCC)). This role leads business planning, execution and enablement of GPS initiatives, communication strategies, resource management, PV forecasting and capacity planning, talent calibration, and the PV functional-level vendor strategy.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Define and communicate the GPS vision and strategy in alignment with enterprise goals and business priorities </p></li><li><p>Serve as a strategic thought partner to the SVP of Global Patient Safety regarding PV strategy, and operating model </p></li><li><p>Act as a strategic connector across GPS teams to enable execution of GPS vision, strategy and priorities </p></li><li><p>Lead strategy and governance for the Global Capabilities Center (GCC) across GPS functions, aligning scope, resourcing, and metrics to GPS priorities and enterprise objectives, to expand PV capacity and drive measurable outcomes </p></li><li><p>Lead development of annual department operating plans and strategic roadmaps for GPS </p></li><li><p>Drive operational excellence in collaboration with GPS leaders, through benchmarking and continuous improvement </p></li><li><p>Partner with GPS interfacing functions to enable PV operational alignment </p></li><li><p>Collaborate with GPS leadership on goal setting, initiative tracking, and performance dashboards </p></li><li><p>Lead delivery of key GPS functional meetings (e.g., GPS Leadership Team, All Hands, Mid-Year meetings). </p></li><li><p>Prepare and maintain regular delivery of GPS communications </p></li><li><p>Organize and manage mid-year and year-end talent calibration exercises in collaboration with stakeholders and HR Business Partners (HRBPs) </p></li><li><p>In partnership with RA GPS DQ Strategy and Operations and Portfolio Management, establish operational portfolio forecasting for GPS </p></li><li><p>Lead resource planning and optimization across GPS functions (internal staffing, GCC expansion, vendor utilization) in partnership with stakeholder functions (e.g., Vendor Relationship Management, GD Resource Management, RA GPS DQ Strategy Planning & Operations, and Portfolio Management) </p></li><li><p>Collaborate cross-functionally in support of GPS with Development Services & Operational Excellence (DS&OE) team, and Learning Center of Excellence (LCoE) functions. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum Bachelor’s Degree (Advanced Degree preferred) in business, strong preference for degree in life sciences or healthcare with 12+ years of relevant PV planning and operations experience in the pharmaceutical area and specific industry experience in managing and providing oversight of operations within a global patient safety organization highly preferred. </p></li><li><p>Proven ability to lead and develop a diverse remit in a constructive, goal-oriented environment, with continuous improvement and innovation mindset. </p></li><li><p>Demonstrated pharmacovigilance (PV) and Safety Risk Management (RM) expertise, including end-to-end safety processes, regulatory expectations, and cross-functional governance within a global patient safety organization </p></li><li><p>Demonstrated problem-solving with the ability to “flex” across different complexities, business situations and cross functional partners of GPS </p></li><li><p>Proven ability to drive results through strong cross-functional partnerships and stakeholder engagement </p></li><li><p>Demonstrated ability and track-record to lead PV operational and planning initiatives with excellence, including governance activities </p></li><li><p>Highly detail-oriented, ensuring accuracy, consistency, and quality across deliverables, documentation, and communications, while maintaining strategic perspective. </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences - Rare Disease]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48141]]></requisitionid>
    <referencenumber><![CDATA[R48141]]></referencenumber>
    <apijobid><![CDATA[r48141]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48141/executive-director-global-patient-safety-sciences-rare-disease/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Executive Director, Global Patient Safety Sciences, Rare Disease is the first point of contact for all Rare Disease strategy-related responsibilities across clinical, and post-marketed drugs in the portfolio. As the product subject matter expert (SME) and Therapeutic Area Head (TAH) for the Rare Disease portfolio, this role defines the product safety strategy, establishes the medical safety opinion, and provides the safety scientific POV across both GPS and non-GPS interactions. In addition, the position acts as a trusted advisor to senior management regarding safety strategies/processes while developing organizational objectives and, importantly, understanding the impact of decisions across functional areas. The ED Global Patient Safety Sciences Rare Disease is responsible for the development of their team, which is comprised of GPS Leads. They will serve as a member of the GPS Leadership Team (GPS LT). </p><p><strong>When & where:</strong> ​​</p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>4 days per week on-site</p></li><li><p>25% travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Contribute senior-level safety expertise to clinical projects across assigned therapeutic area </p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds and serves as point of escalation for ICSR causality assessments </p></li><li><p>Provide oversight for safety signal evaluations & deliver clinical interpretation of emerging safety issues </p></li><li><p>Review benefit-risk assessments (e.g., HHAs) written by Safety Sciences Delivery and recommendations for the product safety profile as appropriate for the stage of the asset lifecycle for safety responses to regulatory agency queries and safety documents (e.g., DSURs, PSURs) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Governance Leadership </em></p><ul><li><p>Influence cross-functional leaders to align priorities and drive enterprise results </p></li><li><p>Approve and provide medical oversight for Risk Management Plans (RMPs) </p></li><li><p>Approve responses to medical & clinical health authority queries as needed </p></li><li><p>Oversee cross-functional Safety Monitoring Team (SMT) activities </p></li><li><p>Represent GPS at cross-functional governance meetings including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT), and with other parties external to Regeneron (e.g., collaborators) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty preferred; MBA is an advantage</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required</p></li><li><p>6+ years of leading a team and people management experience, added benefit if in a matrixed environment </p></li><li><p>Preferred 1-3 years of international pharmaceutical activities </p></li><li><p>Proven track record in developing a deep understanding of the products’ safety profile, supported by in-depth product knowledge to inform safety assessments, risk evaluations, and decision-making </p></li><li><p>Experience with oversight of strategy within a global patient safety organization </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Governance and Contract Compliance, Regeneron Genetics Center (RGC)]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47043]]></requisitionid>
    <referencenumber><![CDATA[R47043]]></referencenumber>
    <apijobid><![CDATA[r47043]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47043/director-data-governance-and-contract-compliance-regeneron-genetics-center-rgc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Director, Data Governance and Contract Compliance leads and ensures compliance across a large portfolio of global data licensing collaborations involving genetic and associated health data. You will serve as Regeneron Genetics Center's (RGC) internal resource on data privacy, genomic data governance, and cross-border data transfer; partnering with RGC counsel, research and technology teams, and the Privacy Office, to uphold the highest standards of data stewardship. You will develop and implement operational policies, procedures, and risk mitigation strategies that enable scientific collaboration, while safeguarding individual data rights worldwide.</p><div><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY or Cambridge, MA</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><ul><li><p>Lead compliance across approximately 150 global data licensing collaborations related to genetic and associated health data, including ongoing monitoring, risk assessment, and remediation.</p></li><li><p>Partner with counsel to interpret and ensure compliance with international privacy regulations (General Data Protection Regulation (GDPR),</p><div>Health Insurance Portability and Accountability Act (HIPAA) ), California Consumer Privacy Act and California Privacy Rights Act (CCPA/CPRA), and genomic data governance frameworks (NIH Genomic Data Sharing Policy, GA4GH), in data collaboration agreements and research operations.</div></li><li><p>Drive the development and operationalization of RGC data governance policies, procedures, consent frameworks, and data use agreements specific to genetic and health data.</p></li><li><p>Lead all aspects of data security stewardship practices, evaluating and integrating emerging privacy-preserving technologies with the IT Security team.</p></li><li><p>Monitor the evolving global regulatory landscape for genetic data governance, advising leadership on compliance risks and policy adaptations.</p></li><li><p>Lead, mentor, and develop a team of data governance and compliance professionals; championing a culture of accountability, transparency, inclusion, and continuous learning.</p></li><li><p>Collaborate cross-functionally with Legal, IT Security, Research, and Business Development to embed privacy-by-design into data collaboration workflows and initiatives.</p></li></ul><p><strong>This role requires: ​</strong></p><ul><li><p>A PhD in Genetics, Genomics, Bioethics, Life Sciences, or a related field; or a relevant degree with experience in data governance and compliance.</p></li><li><p>An equivalent combination of advanced education and 10+ years of experience in data governance, compliance, or regulatory affairs; with at least 5 years focused on genetic or health data in research, biopharmaceutical, or biotech settings.</p></li><li><p>CIPP/E or CIPP/US certifications are strongly preferred.</p></li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44084]]></requisitionid>
    <referencenumber><![CDATA[R44084]]></referencenumber>
    <apijobid><![CDATA[r44084]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44084/calibration-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a Calibration Technician to our growing team. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</p><p><strong>When & Where:</strong></p><p><strong>Location: Rensselaer, NY</strong></p><p><strong>Hours: Training will take place Monday-Friday 8:00am-4:30pm for 3-6 months based on experience level. </strong></p><p><strong>Working hours thereafter will be Sunday-Thursday 10:00pm-8:30am. </strong><strong>Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p><strong>Discover Your Role:</strong></p><ul><li>Calibrating various types of instrumentation including temperature, pressure, level, flow and analytical instruments</li><li>Performing loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Working with medium and low voltages</li><li>Performing basic plumbing and tube bending jobs</li><li>Assisting the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Performing daily Work Orders (WO) and Preventative Maintenance (PM) and efficiently coordinate the workflow and documentation of PMs and WOs</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Following current Good Manufacturing Practices (cGMPs)</li><li>Occasionally working on other facility related work tasks/issues that are outside the calibration department’s normal work duties</li><li>May include planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</li><li>Participation in compliance investigations if and when necessary</li><li>Full gowning required when entering and working on production floor</li><li>Participating in rotation on-call schedule</li><li>Demonstrate basic problem-solving skills</li><li>Are able to learn and follow routine procedures independently as well as part of a team</li><li>Are comfortable and have the flexibility to work in a changing environment</li><li>Can lift, push, and pull at least 50lbs</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p><strong>This Role Requires:</strong></p><p>You must be willing and able to work a <strong>Sunday-Thursday 10:00pm-8:30am schedule.</strong></p><p>Applicants should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p><ul><li>Calibration Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li><li>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I – Allergy/ENT – Manhattan North, NY]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49970]]></requisitionid>
    <referencenumber><![CDATA[R49970]]></referencenumber>
    <apijobid><![CDATA[r49970]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49970/medical-specialist-i-allergyent-manhattan-north-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Manhattan]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p><strong> </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists, Otolaryngologists (ENT) and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently deliver product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Allergy and Otolaryngology (ENT) therapeutic areas to generate product utilization. The MS will develop strong working relationships with Allergy/ENT experts and clinicians in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate in and help lead initiatives to support sales success as assigned (e.g. participate in industry-related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Manhattan North</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven history of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Allergy/ENT/Dermatology market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 14 Aug 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Device Development Engineer (Project Leadership)]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44516]]></requisitionid>
    <referencenumber><![CDATA[R44516]]></referencenumber>
    <apijobid><![CDATA[r44516]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44516/senior-device-development-engineer-project-leadership/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking a Senior Device Development Engineer to join our project lead team. The Sr. Device Development Engineer will drive the end-to-end development of a device combination product and/or platform delivery system, within a specific therapeutic area (Ophthalmic, Immunology/Inflammation, Cardiometabolic, etc.). They will provide comprehensive leadership in engineering product management, regulatory compliance (design controls), and multi-functional collaboration with internal and external partners, for the combination product device.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm </li><li>Travel percentage: 10% domestic & occasionally international</li></ul><p><strong>Discover your role:</strong></p><ul><li>Leads multidisciplinary engineering teams (Human Factors, V&V, Manufacturing, Quality) through the full design and development lifecycle of combination products within the Regeneron pipeline</li><li>Defines product requirements, technical specifications, and design inputs in collaboration with commercial, clinical, and engineering stakeholders; ensures all user needs are validated through design and development</li><li>Understands design inputs/outputs across multiple delivery systems and their impact on end users</li><li>Develops, manages, and communicates program plans, risks, timelines, and budgets to internal and external teams</li><li>Possesses strong project management, interpersonal, analytical, and problem-solving skills</li><li>Integrates device development with CMC and global development timelines; supports internal/external manufacturing teams on design and process information transfer</li><li>Leads product testing and quality assurance processes; ensures a compliant Design History File (DHF) per 21 CFR Part 4 and 21 CFR 820.30</li><li>Supports clinical/commercial regulatory activities related to device development (IND/IMPD, BLA submissions, Clinical Pharmacy Manuals)</li><li>Deep understanding of FDA regulations (21 CFR Part 4, 820.30) and DHF management experience</li><li>Supports strategic product launch and go-to-market planning with therapeutic area device leads</li></ul><p><strong>This role requires: </strong></p><ul><li>BS in Engineering and 5+ years of relevant experience ; or equivalent combination of education & experience.</li><li>Previous experience in product management/project management/ and/or project leadership related activities</li><li>Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Specialist (External Filling)]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49571]]></requisitionid>
    <referencenumber><![CDATA[R49571]]></referencenumber>
    <apijobid><![CDATA[r49571]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49571/quality-assurance-specialist-external-filling/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is seeking a Quality Assurance (QA) Specialist to focus on our external filling operations. This position performs activities supporting dispositioning product and/or raw materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li><li>Travel percentage: 5% domestic</li></ul><p><strong>What you’ll do: </strong></p><ul><li>Reviews and approves executed batch records from external drug product filling sites</li><li>Reviews and approves master batch records from external drug product filling sites</li><li>Represents Quality Assurance in support of complex Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</li><li>Represents the organization on behalf of QA with external partners to communicate QA policy and procedures; liaises with external partners and provides input on regulatory communications</li><li>Trains and/or mentors junior employees, including providing insights and education on processes and procedures</li><li>Provides consultation and advice in alignment with QA policies</li><li>Performs activities associated with disposition of raw materials and product (receipt, inspection, document review, shipping), on the floor or at a desk</li><li>Reviews, edits, or approves Regeneron controlled documents</li><li>Participates in investigations associated with raw materials or product</li><li>Performs status labeling of product</li><li>Continually evaluates Regeneron processes and procedures with an eye toward continuous improvement</li></ul><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Quality Assurance Specialist: 4+ years of experience</li><li>Senior Quality Assurance Specialist: 6+ years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Scientist, Immunology]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50049]]></requisitionid>
    <referencenumber><![CDATA[R50049]]></referencenumber>
    <apijobid><![CDATA[r50049]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50049/senior-manager-clinical-scientist-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Clinical Sciences team, supporting our Immune/Inflammatory clinical development programs. In this role, you will help lead the design, execution, and interpretation of clinical studies, partnering closely with Medical Directors and cross-functional study teams to advance candidates through early and/or late phase development. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY, Cambridge, MA, or Warren, NJ</li></ul><h3>Discover your role:</h3><ul><li>Lead the scientific strategy behind clinical studies from design through execution and reporting</li><li>Partner with Medical Directors and cross-functional teams to shape protocols, amendments, and study conduct</li><li>Build deep expertise in disease biology, compound mechanism of action, and the competitive treatment landscape</li><li>Author and review key trial documents, including expanded synopses, monitoring plans, and study reports</li><li>Safeguard patient safety through ongoing clinical and medical data review</li><li>Identify risks to study integrity early and drive practical mitigation strategies</li><li>Represent Clinical Sciences on program teams, steering committees, and safety monitoring boards</li><li>Champion consistent, high-quality data review practices across assigned studies</li></ul><h3>This role requires:</h3><ul><li>MS, PhD, or PharmD in a related scientific field, plus 8+ years of pharmaceutical clinical drug development experience (other levels considered based on experience)</li><li>Proven knowledge of GCP, ICH guidelines, clinical trial design, and regulatory requirements</li><li>Strong medical writing skills and clinical research methodology expertise</li><li>Experience in Immune/Inflammatory clinical trials preferred</li><li>Demonstrated success working cross-functionally in a matrix organization</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 09:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QC Temp (Day role)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45653]]></requisitionid>
    <referencenumber><![CDATA[R45653]]></referencenumber>
    <apijobid><![CDATA[r45653]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45653/qc-temp-day-role/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Temp </strong><strong><strong>QC A</strong>nalyst</strong> to join our <strong>Quality Control</strong> team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><p>Location<strong>:</strong> Raheen, Limerick, Ireland</p></li><li><p>This is a 12-month contract position</p></li><li><p>This is an onsite role supporting laboratory operations</p></li></ul><h3><strong>What you'll do:</strong></h3><ul><li><p>Perform chemical and biological testing on raw materials, in-process materials, finished products, and stability samples</p></li><li><p>Review and document analytical data, ensuring compliance with quality standards and regulatory requirements</p></li><li><p>Support method validation, technology transfer activities, and continuous improvement initiatives</p></li><li><p>Maintain laboratory equipment, supplies, and documentation in accordance with GMP requirements</p></li><li><p>Collaborate with internal teams and external partners to support quality and operational excellence</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>Thrive working in a laboratory environment with a strong focus on quality and compliance</p></li><li><p>Demonstrate strong attention to detail and accuracy when performing testing and reviewing data</p></li><li><p>Balance multiple priorities while meeting timelines and maintaining regulatory standards</p></li><li><p>Work effectively both independently and as part of cross-functional teams</p></li><li><p>Participate in ongoing training and development activities</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>Requires BS/BA in Life Sciences or related field, or an equivalent combination of education and experience</p></li><li><p>For Associate QC Analyst: 0-2 years of relevant experience</p></li><li><p>For QC Analyst: 2+ years of relevant experience, preferably in a GMP-regulated pharmaceutical or biotechnology environment</p></li><li><p>Strong attention to detail and ability to work effectively in a team-based laboratory environment</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quality Assurance Specialist, On the floor (Overnights)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49584]]></requisitionid>
    <referencenumber><![CDATA[R49584]]></referencenumber>
    <apijobid><![CDATA[r49584]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49584/senior-quality-assurance-specialist-on-the-floor-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Senior Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support QA initiatives for a broad range of topics relative to the start-up and operations of a drug product facility. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work model: 3rd shift, Friday-Tuesday, 10pm-8:30am</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Work on and potentially lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team</p></li><li><p>Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures</p></li><li><p>Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.</p></li><li><p>Maintain project timelines to support the evolving business</p></li><li><p>Perform on-the-floor quality review of documents, such as: equipment logs, training records, testing results, batch records and supporting documents</p></li><li><p>Review and approval of documents (electronic and paper-based)</p></li><li><p>Provide mentorship during on-the-floor manufacturing</p></li><li><p>Support audits, inspections and investigations</p></li><li><p>Perform quarantine, segregation of material and line clearances</p></li><li><p>Contribute to the continuous improvement initiatives</p></li><li><p>Adjust schedule based on facility start up, filling, and manufacturing needs</p></li><li><p>Collaborate with cross-functional internal teams</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Requires B.S in life sciences or related field and 6+ years of experience; may substitute proven experience for education requirement</p></li><li><p>Level will be determined based on experience</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family Care Benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[IT Program Manager – Research & PAPD]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48965]]></requisitionid>
    <referencenumber><![CDATA[R48965]]></referencenumber>
    <apijobid><![CDATA[r48965]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48965/it-program-manager-research-papd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Senior IT Project Analyst will work with the Research, PAPD and IT stakeholders to lead cross-functional technology initiatives, drive portfolio governance, and ensure successful delivery of programs that support Regeneron’s scientific mission. </p><p><strong>When & where:</strong></p><p>Based at our Tarrytown, NY location 4+ onsite per week required – this role is not open to fully remote or hybrid work arrangements.</p><p> <strong>Discover your role:</strong></p><ul><li><p>Leading cross-functional technology initiatives supporting Research and Preclinical Development, driving project planning, execution, risk and dependency management, and timely delivery across multiple concurrent programs </p></li></ul><ul><li><p>Developing and maintaining project roadmaps, milestones, and success metrics to ensure alignment with business objectives; proactively identifying and addressing risks, issues, and opportunities </p></li></ul><ul><li><p>Partnering with Research, PAPD and IT stakeholders to understand business needs and translate them into technology solutions; facilitating decision-making and consensus across diverse stakeholder groups </p></li></ul><ul><li><p>Coordinating activities across business functions, technology teams, vendors, and external partners to support strategic initiatives including integrations, transformations, and process improvement efforts </p></li></ul><p><strong>This role requires:</strong> </p><ul><li><p>A Bachelor’s degree </p></li><li><p>5-7 years of proven experience leading IT projects with a track record of delivering technology initiatives on time and within scope. </p></li><li><p>Previous experience in the biotechnology and/or pharmaceutical industry </p></li><li><p>Proficiency at leading multiple concurrent projects, keeping teams aligned, and delivering results in a fast-paced research environment </p></li><li><p>Expertise at using a variety of tools (e.g., project and portfolio management platforms, reporting dashboards, roadmap and governance frameworks) to drive program execution, monitor portfolio health metrics, and communicate effectively with executive stakeholders.</p></li><li><p>Excitementy around improving effectiveness by leveraging new technologies that are made available on the job, including AI, Analytics and project management tools. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 18:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager International Payroll]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50096]]></requisitionid>
    <referencenumber><![CDATA[R50096]]></referencenumber>
    <apijobid><![CDATA[r50096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50096/manager-international-payroll/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The International Payroll Manager is responsible for the accurate, compliant, and timely delivery of payroll across multiple international locations. This role oversees end-to-end payroll operations, manages third-party payroll vendors, drives process standardization, and partners closely with HR, Finance, Tax, Mobility, Benefits, and Technology teams to ensure payroll excellence and regulatory compliance.</p><p>The ideal candidate is an experienced payroll leader with deep international payroll expertise, strong analytical skills, and a proven ability to manage complex payroll environments while supporting transformation initiatives, system implementations, and process improvements across a global organization.</p><p><em>This role will be based in our Sleepy Hollow, NY offices and requires 4 days per week on-site.</em></p><p><strong>Key Responsibilities</strong></p><div><ul><li><p><strong>International Payroll Operations:</strong> Oversees accurate, compliant end-to-end payroll processing across multiple international regions and countries.</p></li><li><p><strong>Vendor Management:</strong> Manages relationships and performance of global payroll providers while supporting vendor implementations and process improvements.</p></li><li><p><strong>Compliance, Controls & Audit:</strong> Ensures payroll compliance with regulatory requirements, internal controls, audits, and governance standards.</p></li><li><p><strong>Payroll Transformation & Technology:</strong> Leads payroll technology enhancements and transformation initiatives to improve efficiency, accuracy, and scalability.</p></li><li><p><strong>Cross-Functional Partnership:</strong> Collaborates with internal stakeholders to support payroll operations, financial reporting, employee services, and business growth initiatives.</p></li><li><p><strong>Team Leadership:</strong> Develops and leads payroll team members while driving accountability, service excellence, and continuous improvement.</p></li></ul></div><p><strong>Let's See If We're a Fit:</strong></p><ul><li>Bachelor's degree in Accounting, Finance, Business Administration, Human Resources, or related field.</li><li>8+ years of progressive payroll experience with significant international payroll exposure.</li><li>3+ years of people leadership experience.</li><li>This global role is primarily aligned to U.S. business hours and leads payroll operations across Europe and India, requiring flexibility to collaborate across multiple time zones and provide occasional support outside standard working hours to ensure successful payroll delivery and business continuity.</li><li>Strong knowledge of international payroll regulations, taxation, and compliance requirements.</li><li>Experience managing payroll vendors across multiple countries.</li><li>Advanced Excel and analytical skills (pivot tables etc.)</li><li>Strong project management and stakeholder management capabilities.</li><li>International experience with preferred concentration in Europe, India, and Japan.</li></ul><p>Preferred</p><ul><li>Certified Payroll Professional (CPP), IPASS, or equivalent payroll certification.</li><li>Experience with Workday, Oracle Fusion, SAP, ADP GlobalView, CloudPay, or similar global payroll platforms.</li><li>Experience supporting payroll transformation, shared services, or Global Capability Center environments.</li><li>Experience with global mobility, equity, and payroll-related tax processes.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead AI Engineer]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50147]]></requisitionid>
    <referencenumber><![CDATA[R50147]]></referencenumber>
    <apijobid><![CDATA[r50147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50147/lead-ai-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Job Title: </strong>Lead AI Engineer</p><p><strong>Department: </strong>Digital Transformation – AI Strategy & Execution</p><p><strong>Location: </strong>Sleepy Hollow, New York</p><p><strong>Employment Type: </strong>Full-Time</p><p><strong>Experience Required: </strong>7–10 Years</p><h3>About Regeneron</h3><p>Regeneron is a leading biotechnology company headquartered in Tarrytown, New York, renowned for its innovative research and development of life-changing therapies. With a strong focus on ophthalmology, oncology, inflammation, cardiovascular diseases, and infectious diseases, Regeneron has brought groundbreaking medicines to market — including EYLEA® and the REGEN-COV™ monoclonal antibody cocktail. Our commitment to scientific excellence, cutting-edge technology, and patient impact has positioned Regeneron as a global leader in biotechnology.</p><h3>Position Overview</h3><p>Regeneron is seeking an experienced Lead AI Engineer to serve as a technical leader within the AI Strategy & Execution organization. In this role, you will architect and deliver enterprise-scale AI capabilities — spanning intelligent agents, LLM-powered applications, and AI platform services — that accelerate drug discovery, clinical research, and enterprise productivity. You will lead a team of engineers, drive cross-functional collaboration, and communicate AI strategy to senior stakeholders, all while maintaining a strong hands-on presence in Python development and AI systems design.</p><h3>Key Responsibilities</h3><h3>AI Engineering & Intelligent Systems</h3><ul><li>Lead end-to-end design, development, and deployment of enterprise AI applications and LLM-powered systems, ensuring production-grade quality, security, and scalability.</li></ul><ul><li>Design and build AI Agents and autonomous systems using agentic frameworks including LangChain, LangGraph, Strands, and CrewAI, applying ReAct, tool-use, planning, and memory management patterns.</li></ul><ul><li>Develop and operate MCP (Model Context Protocol) servers for standardized, secure integration between AI agents and enterprise data sources.</li></ul><ul><li>Apply advanced LLM techniques — prompt engineering, fine-tuning, and retrieval-augmented generation (RAG) — to build intelligent, context-aware applications.</li></ul><ul><li>Architect and manage vector database solutions (Milvus DB preferred) supporting semantic search, knowledge retrieval, and RAG pipelines.</li></ul><ul><li>Architect RESTful APIs that expose AI capabilities to internal platforms and downstream business applications.</li></ul><h3>LLM & AI Platform Management</h3><ul><li>Administer and continuously evolve the enterprise LLM and AI Gateway platform, including model routing, access controls, rate limiting, usage observability, and multi-model orchestration.</li></ul><ul><li>Evaluate and onboard new foundation models (OpenAI, Anthropic, AWS Bedrock, and others) in alignment with enterprise security and compliance standards.</li></ul><h3>Technical Leadership & Team Management</h3><ul><li>Lead, mentor, and manage a team of AI engineers, conducting code reviews, setting technical standards, and fostering a culture of engineering excellence.</li></ul><ul><li>Contribute to the organization’s AI roadmap through architectural design reviews, technical strategy, and proof-of-concept development.</li></ul><ul><li>Troubleshoot complex issues across AI model serving, APIs, and platform layers.</li></ul><h3>Cross-Functional Collaboration & Stakeholder Engagement</h3><ul><li>Partner with business units, data scientists, and clinical research teams to identify AI opportunities and translate them into scalable technical solutions.</li></ul><ul><li>Serve as the primary technical point of contact for enterprise AI platform discussions, presenting findings and recommendations to senior leadership.</li></ul><ul><li>Engage with external vendors, cloud providers, and AI research organizations to evaluate and integrate emerging capabilities.</li></ul><h3>Requirements & Qualifications</h3><h3>Education</h3><ul><li>Bachelor’s, Master’s, or Ph.D. in Computer Science, Computer Engineering, Artificial Intelligence or a related technical field.</li></ul><h3>Experience</h3><ul><li>7–10 years of progressive software and AI engineering experience, with at least 3 years in a technical lead or senior individual contributor role.</li></ul><ul><li>Expert-level Python development skills, including production REST API development with FastAPI.</li></ul><ul><li>Proven hands-on experience building AI Agents, MCP Servers, and LLM-powered applications using frameworks such as LangChain, LangGraph, Strands, or CrewAI.</li></ul><ul><li>Hands-on experience with vector databases (Milvus DB preferred) for RAG and semantic search pipelines.</li></ul><ul><li>Experience administering LLM API gateway platforms, including model routing, observability, access governance, and multi-model orchestration.</li></ul><ul><li>Experience with foundation models from OpenAI, Anthropic, AWS Bedrock, and other major providers.</li></ul><ul><li>Working knowledge of AWS cloud services relevant to AI workloads (SageMaker, Bedrock, EKS, Lambda, S3); Kubernetes and CI/CD experience is a plus.</li></ul><ul><li>Experience in the biotechnology, pharmaceutical, or healthcare industry preferred.</li></ul><h3>Technical Competencies</h3><ul><li>Programming: Python (expert-level).</li></ul><ul><li>AI Frameworks & Runtimes: LangChain, LangGraph, Strands, CrewAI; AWS Bedrock AgentCore.</li></ul><ul><li>LLM Techniques: Prompt engineering, fine-tuning, RAG, vector databases (Milvus DB preferred).</li></ul><ul><li>AI Platform: LLM Gateway management, model routing, multi-model orchestration, TensorFlow, PyTorch.</li></ul><ul><li>API Development: RESTful API design, FastAPI, OpenAPI/Swagger.</li></ul><ul><li>Cloud & Infrastructure (supporting): AWS (SageMaker, Bedrock, EKS, Lambda, S3), Kubernetes, Docker, Terraform, CI/CD pipelines.</li></ul><ul><li>Data & Analytics: Databricks, Dataiku, Postgres, Redis, NoSQL databases.</li></ul><ul><li>Observability: Monitoring, logging, and distributed tracing for AI workloads.</li></ul><h3>Certifications</h3><p><strong>Required:</strong></p><ul><li>AWS Certified Machine Learning – Specialty</li></ul><p><strong>Nice to Have:</strong></p><ul><li>AWS Certified Solutions Architect – Professional</li></ul><ul><li>Certified Kubernetes Administrator (CKA)</li></ul><h3>Soft Skills & Leadership</h3><ul><li>Exceptional communication skills with the ability to present AI concepts to both engineering teams and executive stakeholders.</li></ul><ul><li>Proven track record of leading engineering teams and managing delivery across cross-functional groups.</li></ul><ul><li>Strong problem-solving mindset with a bias toward pragmatic, production-ready AI solutions.</li></ul><ul><li>Collaborative and proactive in engaging with business units, compliance, and external partners.</li></ul><p><em>Joining Regeneron as a Lead AI Engineer offers a unique opportunity to shape enterprise AI strategy, build transformative platforms, and make a meaningful impact on the advancement of global healthcare. If you are a driven technical leader with deep expertise in AI systems and a passion for innovation in a regulated environment, we invite you to apply.</em>Please copy and paste the desired job description for this role here. If you need a copy of an existing job description please reach out to TA or work with your HR Business Partner to develop one for a new role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - South Central]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48156]]></requisitionid>
    <referencenumber><![CDATA[R48156]]></referencenumber>
    <apijobid><![CDATA[r48156]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48156/neurology-account-director-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: South Central (Texas, Arkansas and Louisiana)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - COLUMBUS, OH]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48007]]></requisitionid>
    <referencenumber><![CDATA[R48007]]></referencenumber>
    <apijobid><![CDATA[r48007]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48007/medical-account-specialist-ii-neurology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Columbus (Metro), OH</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LITTLE ROCK, AR]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48057]]></requisitionid>
    <referencenumber><![CDATA[R48057]]></referencenumber>
    <apijobid><![CDATA[r48057]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48057/medical-account-specialist-ii-neurology-little-rock-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Little Rock]]></city>
    <state><![CDATA[Arkansas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Little Rock (Metro), AR</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MANCHESTER, NH]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48000]]></requisitionid>
    <referencenumber><![CDATA[R48000]]></referencenumber>
    <apijobid><![CDATA[r48000]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48000/medical-account-specialist-ii-neurology-manchester-nh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Manchester]]></city>
    <state><![CDATA[New Hampshire]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Manchester, NH</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) – ONCOLOGY *TOKYO AREA]]></title>
    <date><![CDATA[Mon, 22 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48621]]></requisitionid>
    <referencenumber><![CDATA[R48621]]></referencenumber>
    <apijobid><![CDATA[r48621]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48621/medical-representative-mr-oncology-startokyo-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist, Oncology to join our Oncology Sales team, supporting our oncology business area in a field-based role. In this role, you will drive the adoption of our oncology product portfolio while collaborating with healthcare professionals and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>You will be responsible for the Tokyo area.</p><p>While we assume living within Tokyo's 23 wards, we are also open to discussion regarding those living outside of Tokyo's 23 wards, Saitama, Chiba, and Kanagawa prefectures, depending on the specific area.</p><br><p><strong>Discover your role:</strong></p><ul><li>Drive sales and adoption of the oncology product portfolio within assigned territory</li><li>Develop and execute territory business plans to achieve sales targets</li><li>Build and maintain relationships with healthcare professionals and key accounts</li><li>Deliver approved scientific and clinical information to support customer decisions</li><li>Identify and engage new business opportunities in the oncology space</li><li>Collaborate with cross-functional teams to support customer needs</li><li>You adapt to evolving priorities and thrive in a results-driven environment</li><li>You demonstrate strong communication and relationship-building skills</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in life sciences, business, or related field</li><li>Proven sales experience in the pharmaceutical, biotech, or healthcare industry</li><li>Knowledge of oncology or related therapeutic area</li><li>Strong communication, presentation, and negotiation skills</li><li>Ability to travel within assigned territory as required</li><li>Driver license and MR certification</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Commercial Procurement]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48237]]></requisitionid>
    <referencenumber><![CDATA[R48237]]></referencenumber>
    <apijobid><![CDATA[r48237]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48237/manager-commercial-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Commercial Category Management Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will lead category management enablement, transform data into actionable insights, and support global category strategies while collaborating with global procurement teams, data and analytics partners, and key collaborators. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead a team of associates and specialists to transform market intelligence and analytics into actionable insights that enable global category management strategy development.</p></li><li><p>Support the definition and implementation of global commercial category strategies aligned to regional and global business needs.</p></li><li><p>Deliver micro and macro market analysis, spend insights, supplier evaluation, and risk assessments to support strategy and partner engagement.</p></li><li><p>Partner with data and analytics teams to demonstrate internal and external data sources to identify trends, opportunities, and future strategy direction.</p></li><li><p>Facilitate sourcing processes by supporting RFP, RFQ, and RFI development and managing response collection, analysis, and comparative evaluations</p></li><li><p>Maintain and optimize category management templates, strategy decks, and stage-gate materials, ensuring consistent tools and repository governance.</p></li><li><p>Track and report internal requests handled by the category management enablement team in line with engagement plans and delivery commitments.</p></li><li><p>You foster collaboration, lead through influence, and operate with clarity and integrity in a global, matrixed, and evolving environment.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive experience in procurement, preferably in Pharma/Biopharma</p></li><li><p>Proven experience leading teams, processes, and suppliers across multiple categories in a global or multi-national environment</p></li><li><p>Strong knowledge of category management principles, including market analysis, spend analysis, supplier evaluation, and risk management</p></li><li><p>Demonstrated expertise in transforming data and market intelligence into actionable category insights and strategies</p></li><li><p>Experience leading and developing associate- and specialist-level professionals, including performance management, coaching, and career development.</p></li><li><p>Ability to build influential relationships with partners and suppliers to drive business outcomes.</p></li><li><p>Working knowledge of ERP systems and Source-to-Pay (S2P) platforms (e.g., Oracle, Zycus, GEP, Ariba) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint).</p></li><li><p>Ability to operate effectively with integrity, focus, and clarity in ambiguous environments and inspire change and improvement.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, Clinical Data Reporting]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48587]]></requisitionid>
    <referencenumber><![CDATA[R48587]]></referencenumber>
    <apijobid><![CDATA[r48587]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48587/specialist-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist, Clinical Data Reporting to join our Data Management team, supporting clinical trial oversight and study-level data review in a hybrid role. In this role, you will produce accurate and consistent reporting outputs that drive data cleaning, medical review, and operational decision-making, while collaborating with clinical data management, technology partners, and cross-functional teams to deliver study-level reports on schedule. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Program and maintain standardized clinical data reports and listings used for participant-level data review, data cleaning, and operational oversight</p></li><li><p>Translate study reporting requirements into technical specifications and implement outputs using established frameworks and data standards</p></li><li><p>Build and validate data review listings, exception reports, reconciliation outputs between EDC and external data, and operational performance reports</p></li><li><p>You communicate clearly with cross-functional partners to clarify reporting needs and deliver outputs on schedule</p></li><li><p>Partner with clinical data management and technology teams to leverage data sources including the Scientific Data Lake, EDC systems, and external data streams</p></li><li><p>Monitor routine data refreshes, troubleshoot issues with accuracy, completeness, and integration, and contribute to automation and workflow streamlining</p></li><li><p>Keep reporting documentation, specifications, and outputs audit- and inspection-ready in line with GCP, ICH, GDPR, SOPs, and internal quality standards</p></li><li><p>You stay curious about reporting tools and methodologies, sharing knowledge of standards and processes to support team learning and continuous improvement</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's or Master's degree in Data Science, Computer Science, Life Sciences, or a related field</p></li><li><p>2+ years of experience in clinical data, data visualization, or related disciplines, with a background in building interactive reporting solutions, KPIs, and metrics to support clinical trial oversight</p></li><li><p>Proficiency in EDC systems (e.g., Medidata RAVE) and analytics, reporting, and data visualization tools such as SAS, R, Python, JReview, elluminate, Tableau, Power BI, or Spotfire</p></li><li><p>Strong understanding of clinical trial processes, clinical data standards (e.g., CDISC), and regulatory requirements (GCP, GDPR, HIPAA)</p></li><li><p>Experience with risk-based data review concepts, data quality standards, and data lifecycle management in a regulated environment</p></li><li><p>Experience with data lakes, data pipelines, data integration, automation, and reporting and analytics in a clinical research environment</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (New York, Metro)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48126]]></requisitionid>
    <referencenumber><![CDATA[R48126]]></referencenumber>
    <apijobid><![CDATA[r48126]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48126/field-reimbursement-manager-neurology-new-york-metro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: New York, (Metro) NY</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, R&D Chemistry]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48744]]></requisitionid>
    <referencenumber><![CDATA[R48744]]></referencenumber>
    <apijobid><![CDATA[r48744]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48744/senior-associate-scientist-rd-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Senior Associate Scientist, R&D Chemistry Job Description</strong></p><p>We are currently seeking a synthetic organic chemist for the R&D (Research & Development) Chemistry group. In this position, they will play an important role in supporting Regeneron small molecule antibody-conjugate drug discovery capabilities, providing an important link with the company’s existing expertise in biologics and novel genetic medicines. The candidate will enable in-house laboratory-based synthetic chemistry activities towards the discovery and generation of novel small-molecule payloads and linkers for antibody-drug conjugate therapeutics across research areas of oncology, metabolic disease/obesity, infectious diseases, immunology and inflammation, neuroscience, and ophthalmology. Cultural fit with the Regeneron chemistry and cross-functional teams is a priority. The R&D Chemistry team is composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have small-molecule synthetic organic background and experience with the retrosynthetic analysis, synthetic route design, and hands-on execution of multistep synthetic protocols including compound isolation and characterization. A firm understanding of modern organic synthesis strategies and techniques and the ability to work independently while deploying them in a fit-for-purpose efficient approach to biologically active targets of interest will be the key. Ability to interpret spectroscopic data in the assignment/ confirmation of small molecule structures is required. Knowledge of the latest synthetic methods utilized in the antibody-conjugate linker generation is a plus.</p><p><strong>A day in the life of a Senior Associate Scientist – R&D Chemistry may look like:</strong></p><ul><li>Perform the day-to-day laboratory activities as part of the R&D Chemistry group, providing experimental execution of small-molecule syntheses and the associated compound isolation and characterization.</li><li>Troubleshoot, analyze data, interpret experimental results and propose synthetic approaches to new targets.</li><li>Discuss biological data and new targets within the existing projects to address structure-activity relationship directions.</li><li>Identify new strategies and technologies best suited for synthetic execution of the targets of interest.</li><li>Work within the priorities set by the cross-functional teams and your supervisor. Ensure successful progression of the group’s technology and pipeline projects.</li><li>Participate in departmental, cross-functional meetings to contribute expertise and to represent the goals of the R&D Chemistry group.</li><li>Interact broadly and collaboratively with other Regeneron groups.</li></ul><p><strong>This might be the right role for you if:</strong></p><ul><li>You are passionate and enthusiastic about the promise of small molecule-based, antibody-targeted therapeutics and appreciate the challenges of synthetic chemistry and drug design.</li><li>You enjoy developing solutions for synthesis and advancing structure-activity relationships within medicinal chemistry drug discovery programs.</li><li>You are comfortable working as part of a cross-functional team.</li><li>You want to be a part of the organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li></ul><p><strong>To be considered for this role, you must:</strong></p><p>Have a M.Sc. in synthetic organic chemistry (or related), and familiarity with drug discovery processes and modern methods of synthetic organic and medicinal chemistry.</p><p>Bonus experience would include general understanding of the process of biological target validation, ADME/PK, PD/efficacy and of the ways that medicinal chemistry contributes to the progress in these areas.</p><p>A minimum of 5-7 years of industry drug discovery experience with small molecules is required. Familiarity with peptidomimetics or antibody-targeted therapeutics is a plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Commercial Insights & Analytics International]]></title>
    <date><![CDATA[Wed, 15 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49376]]></requisitionid>
    <referencenumber><![CDATA[R49376]]></referencenumber>
    <apijobid><![CDATA[r49376]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49376/associate-director-commercial-insights-analytics-international/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Commercial Insights & Analytics International to join our Commercial Insights and Analytics team, supporting Neurology across Europe, Japan and Canada in a hybrid model. In this role, you will enable informed decision making while collaborating with above-market teams, local teams, IT, sourcing and vendors.</p><p>Reporting to the Director, Insights and Analytics International, this position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When</strong> <strong>&</strong> <strong>where:</strong></p><p>Madrid - supporting international markets across Europe, Japan and Canada.</p><p>Hybrid work model - Office based</p><p><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></p><ul><li><p>Be responsible for international performance analytics and reporting for evolving business needs.</p></li><li><p>Lead customer insights, market research and reporting deliverables for Neurology.</p></li><li><p>Implement above-country market research and objective secondary data analyses.</p></li><li><p>Build patient cohorts, treatment journeys and patient flow forecasts.</p></li><li><p>Develop account-level insights, including segmentation and opportunity assessments.</p></li><li><p>Partner with Commercial Operations on field sizing, targeting and incentive analyses.</p></li><li><p>Centralize data management needs with business leaders, IT and sourcing.</p></li><li><p>You create clear insights that connect business implications with practical options.</p></li></ul><p><strong>This</strong> <strong>role</strong> <strong>requires:</strong></p><ul><li><p>8+ years of relevant experience, including 4+ years in market research.</p></li><li><p>Above-country analytics and market research experience in international pharmaceutical markets.</p></li><li><p>Understanding of biopharmaceutical commercial dynamics, laws and regulations.</p></li><li><p>Knowledge of data industry standards and data asset procedures.</p></li><li><p>Expertise in data visualization, data storytelling and report creation tools.</p></li><li><p>Proficiency in Microsoft PowerPoint, Excel, Word and Veeva.</p></li><li><p>Practical experience with Power BI, QlikView, Tableau, Oracle BI, MicroStrategy, Cognos or Spotfire.</p></li><li><p>Strong project, change management, presentation, communication and collaboration skills.</p></li><li><p>English language skills; with one additional language including German, French, Italian or Japanese preferred.</p></li><li><p>Prior biopharmaceutical field sales or marketing experience is desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€81,300.00 - €135,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Commercial Insights & Analytics International]]></title>
    <date><![CDATA[Wed, 15 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49377]]></requisitionid>
    <referencenumber><![CDATA[R49377]]></referencenumber>
    <apijobid><![CDATA[r49377]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49377/associate-director-commercial-insights-analytics-international/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Commercial Insights & Analytics International to join our Commercial Insights and Analytics team, supporting Neurology across Europe, Japan and Canada in a hybrid model. In this role, you will enable informed decision making while collaborating with above-market teams, local teams, IT, sourcing and vendors.</p><p>Reporting to the Director, Insights and Analytics International, this position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When</strong> <strong>&</strong> <strong>where:</strong></p><p>Milan - supporting international markets across Europe, Japan and Canada.</p><p>Hybrid work model - Office based</p><p><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></p><ul><li><p>Be responsible for international performance analytics and reporting for evolving business needs.</p></li><li><p>Lead customer insights, market research and reporting deliverables for Neurology.</p></li><li><p>Implement above-country market research and objective secondary data analyses.</p></li><li><p>Build patient cohorts, treatment journeys and patient flow forecasts.</p></li><li><p>Develop account-level insights, including segmentation and opportunity assessments.</p></li><li><p>Partner with Commercial Operations on field sizing, targeting and incentive analyses.</p></li><li><p>Centralize data management needs with business leaders, IT and sourcing.</p></li><li><p>You create clear insights that connect business implications with practical options.</p></li></ul><p><strong>This</strong> <strong>role</strong> <strong>requires:</strong></p><ul><li><p>8+ years of relevant experience, including 4+ years in market research.</p></li><li><p>Above-country analytics and market research experience in international pharmaceutical markets.</p></li><li><p>Understanding of biopharmaceutical commercial dynamics, laws and regulations.</p></li><li><p>Knowledge of data industry standards and data asset procedures.</p></li><li><p>Expertise in data visualization, data storytelling and report creation tools.</p></li><li><p>Proficiency in Microsoft PowerPoint, Excel, Word and Veeva.</p></li><li><p>Practical experience with Power BI, QlikView, Tableau, Oracle BI, MicroStrategy, Cognos or Spotfire.</p></li><li><p>Strong project, change management, presentation, communication and collaboration skills.</p></li><li><p>English language skills; with one additional language including German, French, Italian or Japanese preferred.</p></li><li><p>Prior biopharmaceutical field sales or marketing experience is desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€79,800.00 - €133,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I - Purification Automation]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48634]]></requisitionid>
    <referencenumber><![CDATA[R48634]]></referencenumber>
    <apijobid><![CDATA[r48634]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48634/process-development-engineer-i-purification-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer I</strong> to join our Preclinical Manufacturing & Process Development (PMPD) Purification team. In this role, you will focus on the development, deployment, and continuous improvement of custom automated systems used in process development laboratories and pilot-scale environments, collaborating closely with internal stakeholders to identify operational bottlenecks and design solutions that reduce manual interaction with equipment and improve data accessibility.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide, working across the full system lifecycle from concept through deployment.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site, supporting process development laboratories and pilot-scale environments</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support automation systems and equipment</li></ul><h3><strong>What you'll do:</strong></h3><p><em>Automation System Development & Deployment</em></p><ul><li>Design, build, and deploy custom automation solutions for laboratory and pilot-scale process development equipment</li><li>Collaborate with internal stakeholders to define requirements, identify bottlenecks, and develop solutions to improve workflow efficiency and data capture</li><li>Participate in the full system lifecycle: concept development, design, procurement, assembly, controls development, testing, deployment, and technology transfer</li><li>Develop control logic (e.g., PLC or equivalent), human-machine interfaces (HMIs), and supporting software for automated systems</li><li>Troubleshoot and resolve issues with custom-built automation systems and supporting infrastructure</li></ul><p><em>Support, Maintenance, and Continuous Improvement</em></p><ul><li>Maintain and improve existing automation systems to ensure reliability, performance, and usability</li><li>Identify and implement enhancements to reduce manual intervention, improve robustness, and increase scalability</li><li>Monitor system performance and proactively address issues impacting system uptime or data integrity</li></ul><p><em>Data Integration & Infrastructure</em></p><ul><li>Support integration of equipment and automation systems with data platforms and PI historian</li><li>Develop and maintain data flows enabling monitoring, trending, reporting, and future advanced control capabilities</li><li>Assist in troubleshooting communication issues between devices, control systems, and data infrastructure</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is an on-site role based across process development laboratories and pilot-scale environments, requiring close collaboration across software, electrical, mechanical, and process development disciplines.</li><li>Flexibility to manage multiple projects and priorities simultaneously, and to troubleshoot system issues as they arise, is required.</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><h3>Must-haves:</h3><ul><li>Bachelor's degree with 3-5 years of experience, or Master's degree with 0-2 years of experience, in Engineering (e.g., Chemical, Mechanical, Electrical, Biomedical) or a related field</li><li>Strong background in downstream bioprocessing (e.g., filtration, chromatography, pilot-scale operations) OR a strong background in automation, controls, or software development</li><li>Strong problem-solving and troubleshooting skills, with a detail-oriented focus on reliability and system performance</li><li>Ability to communicate technical concepts and project progress to cross-functional stakeholders, and to prepare and maintain documentation including system designs and technical reports</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Experience with industrial automation and control systems</li><li>Programming experience (e.g., Python or similar)</li><li>Experience developing control logic (e.g., sequential function charts, state-based control)</li><li>Familiarity with industrial communication protocols (e.g., OPC, Modbus TCP)</li><li>Experience with SCADA/HMI platforms (e.g., Ignition or similar)</li><li>Experience with data historians or data infrastructure (e.g., AVEVA PI or similar)</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - TACOMA, SPOKANE, WA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48959]]></requisitionid>
    <referencenumber><![CDATA[R48959]]></referencenumber>
    <apijobid><![CDATA[r48959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48959/medical-account-specialist-ii-hematology-tacoma-spokane-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tacoma]]></city>
    <state><![CDATA[Washington]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: Tacoma/Spokane, WA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - Neurology (Mid South)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48132]]></requisitionid>
    <referencenumber><![CDATA[R48132]]></referencenumber>
    <apijobid><![CDATA[r48132]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48132/field-reimbursement-manager-neurology-mid-south/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Richmond, VA, Raleigh, NC, Columbia, SC, Lexington, KY, Charlotte, NC, Nashville, TN, Cincinnati, OH & Knoxville, TN<br> </li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement- Advanced Therapies]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46026]]></requisitionid>
    <referencenumber><![CDATA[R46026]]></referencenumber>
    <apijobid><![CDATA[r46026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46026/senior-manager-global-procurement-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Global Procurement – Advanced Therapies to join our Global Procurement organization, supporting our Contract Development and Manufacturing Organization (CDMO) category on an on-site basis. In this role, you will lead end-to-end procurement strategies and drive global category execution across Contract Development and Manufacturing Operations, while collaborating with Procurement management, business partners, and the Law department to align category priorities and deliver cost savings and efficiency gains.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Schedule: Mon-Fri 8:00am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Defines and implements the global CMO Category strategy to serve global and regional business needs</p></li><li><p>Aligns category priorities with Procurement management and business partners through close cross-functional collaboration</p></li><li><p>Manages negotiations, supplier management, and partner engagement activities for the Packaging Category</p></li><li><p>Drives cost savings, cash flow improvement, and other efficiency gains through category management activities</p></li><li><p>Participates in organizational decisions within CMO categories that carry critical short- and long-term impact on category performance</p></li><li><p>Leads category activities to ensure compliance with GxPs and other applicable regulations</p></li><li><p>Negotiates contract terms and conditions in consultation with the Law department, aligned with Regeneron's priorities</p></li><li><p>Uses data and market knowledge to drive decision-making and continuous improvement across category projects</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Sr Manager Level: Bachelor's degree in a relevant field and 8+ years of progressive experience in procurement, including experience in Pharma/BioPharma or science in general, demonstrating growth in experience, scale, and development throughout</p></li><li><p>Experience managing teams of professional-level employees responsible for category management tasks (if applicable)</p></li><li><p>Preferred/nice-to-have: Working knowledge of sourcing and contracting tools, ERPs, and eRFx systems (e.g., Oracle, Zycus, Ariba)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (f/m/d) - Köln - Bonn - Eifel]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49173]]></requisitionid>
    <referencenumber><![CDATA[R49173]]></referencenumber>
    <apijobid><![CDATA[r49173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49173/sales-specialist-oncology-fmd-koeln-bonn-eifel/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist Oncology (f/m/d) to represent our Oncology division across the Köln (Cologne) - Bonn - Eifel territory. In this role, you will build strong relationships with Healthcare Professionals (HCPs), identify key opinion leaders, and tailor your approach to individual and account needs, all in service of bringing our Oncology portfolio to the patients who need it. This is an opportunity to bring a "patient first" mindset to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><p>Field-based in Köln - Bonn - Eifel territory</p><p><strong>Discover your role:</strong></p><ul><li><p>Establish and lead high-quality HCP interactions by keeping your scientific knowledge of the product, indication, and brand sales messaging current, and reliably implementing sales & marketing plans</p></li><li><p>Consistently deliver on the brand's value proposition, ensuring objectives are met through clear key message communication to HCPs</p></li><li><p>Manage your territory with professional account planning, applying a targeting & segmentation approach aligned with regional and country-level guidance</p></li><li><p>Develop and implement a local account plan grounded in key data sources and local market insights, in line with the Germany Brand Plan</p></li><li><p>Collaborate closely with medical colleagues to implement regional programmes and activities that support HCP needs</p></li><li><p>Leverage all communication channels, including digital, in collaboration with other functions, to achieve the best possible share of voice in the market</p></li><li><p>Report results and developments proactively and clearly to the Germany leadership team</p></li></ul><p><br> </p><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent experience, plus a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</p></li><li><p>5+ years of sales experience within the biotech / pharmaceutical sector, including experience in Oncology</p></li><li><p>Proficiency in German, plus conversational English</p></li><li><p>A deep understanding of the local healthcare economy, with the ability to identify key players in Oncology</p></li><li><p>A "patient first" value system</p></li><li><p>Readiness for very frequent travel and a Class 3/B driver's licence</p></li></ul><p><br>Salary range (annually)</p><p>73,125 -121,875 €</p><div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Okayama, Hiroshima Area]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47551]]></requisitionid>
    <referencenumber><![CDATA[R47551]]></referencenumber>
    <apijobid><![CDATA[r47551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47551/medical-representative-mr-dermatology-starokayama-hiroshima-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Sales Representative Dermatology Japan Region to join our commercial team, supporting Japan in a field-based work mode. In this role, you will achieve dermatology sales objectives and deliver customer value while collaborating with sales leadership, marketing teams, and alliance partners. This position offers the opportunity to supply to a fast-growing, science-driven organization making a relevant difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Okayama or Hiroshima, Japan</p><p>Work model: Field-based</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Achieve dermatology sales objectives through territory budget management.</li><li>Develop and update annual territory business plans using market insights.</li><li>Build territory action plans using key data sources.</li><li>Deliver disease-focused customer engagement and value-based solutions.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Partner with alliance teams to achieve shared business objectives.</li><li>Follow regulatory, legal, and company compliance requirements.</li><li>You act strategically and lead priorities to enhance customer impact.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree or equivalent.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Valid driver license and MR Certification.</li><li>Strong customer engagement skills with a focus on delivering value.</li><li>Technical proficiency and ability to conduct disease and concept selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and audience-focused communication skills.</li><li>Ability to implement strategic and tactical plans independently under tight timelines.</li><li>Computer proficiency in word processing, spreadsheets, databases, and email software.</li><li>Alliance partnership experience.</li><li>Dermatology knowledge and biologics sales experience preferred.</li><li>Current clinical knowledge of relevant therapy areas and competitor brands preferred.</li><li>Established Key Opinion Leader relationships within dermatology preferred.</li><li>English fluency is a plus.</li><li>Willingness to travel and work evenings or weekends when required.</li><li>Dedication to training completion, safe driving practices, and company policies.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Oncology - Irvine, CA]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49851]]></requisitionid>
    <referencenumber><![CDATA[R49851]]></referencenumber>
    <apijobid><![CDATA[r49851]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49851/medical-specialist-ii-oncology-irvine-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Irvine]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><br><h3>When & where:</h3><ul><li>Reside in the greater Irvine, CA region</li></ul><br><h3>Discover your role:</h3><ul><li>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelors degree; Master’s degree or additional advanced education/certifications a plus and</li><li>Minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred).</li><li>Buy and bill experience with biologics required.</li><li>Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions.</li><li>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks.</li><li>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization.</li><li>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</li></ul><p><strong>Salary range (annually)</strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager - Facilities, Capital & Logistics  Procurement]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48235]]></requisitionid>
    <referencenumber><![CDATA[R48235]]></referencenumber>
    <apijobid><![CDATA[r48235]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48235/associate-manager-facilities-capital-logistics-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager Global Procurement Facilities Capital & Logistics to join our Global Procurement team, supporting our global Facilities, Capital & Logistics categories in a hybrid work model. In this role, you will support global category strategy, sourcing, negotiations, supplier management, and procurement decisions while collaborating with customers, suppliers, Procurement colleagues, and the Law department. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><br><h3><strong>Discover your role:</strong></h3><ul><li><p>Support the definition and implementation of global Facilities, Capital & Logistics category strategies aligned with global and regional business needs.</p></li><li><p>Partner with team members and Procurement leadership to align category priorities and manage category-related discussions.</p></li><li><p>Manage sourcing activities, supplier relationships, negotiations, and stakeholder engagement across assigned categories.</p></li><li><p>Drive value through cost savings, cash flow improvements, and operational efficiencies from category management initiatives.</p></li><li><p>Negotiate contract terms and conditions in collaboration with the Law department to support business requirements.</p></li><li><p>Use data, market insights, and supplier engagement to guide category decisions and improve procurement outcomes.</p></li><li><p>Coach procurement technical skills across the Global Procurement organization and contribute to team capability development.</p></li><li><p>Bring integrity, focus, and clarity to help motivate change and continuous improvement in a dynamic environment.</p></li></ul><br><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field of study.</p></li><li><p>Relevant progressive procurement experience, including experience within the Pharma or BioPharma industry.</p></li><li><p>Experience managing category processes and suppliers across multiple categories.</p></li><li><p>Demonstrated success working with cross-functional teams to deliver results across Facilities, Capital & Logistics categories or related categories through sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Knowledge of rates, unit costs, and costing structures to support effective negotiations.</p></li><li><p>Experience using external data sources, market intelligence, supplier engagement, and supply market insights to support category strategies.</p></li><li><p>Demonstrated success supporting global supply market evaluation using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Experience supporting key supplier relationship management activities.</p></li><li><p>Experience operating effectively with integrity, focus, and clarity in environments of ambiguity and change.</p></li><li><p>Experience managing associate-level professionals preferred.</p></li><li><p>Working knowledge of sourcing and contracting tools, Enterprise Resource Planning (ERP) systems, and electronic Request for Proposal (eRFX) platforms, including Oracle, Zycus, Ariba, or similar systems.</p></li><li><p>Ability to employ standard business applications including Word, Excel, and PowerPoint for communication, presentation, and analysis.</p></li><li><p>Strong data-driven decision-making skills for category management and procurement projects.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46213]]></requisitionid>
    <referencenumber><![CDATA[R46213]]></referencenumber>
    <apijobid><![CDATA[r46213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46213/principal-statistical-programmer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><p>Location: Warren, NJ or Cambridge, MA</p></li><li><p>Work model/flexibility: onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Support or lead programming and quality control of analysis datasets, tables, listings, and graphs</p></li><li><p>Coordinate activities and communicate shifting timelines and milestones to the study team</p></li><li><p>Create and maintain programming specifications for analysis datasets across studies</p></li><li><p>Support creation and validation of submission requirements, including annotated CRFs and define documents</p></li><li><p>Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch</p></li><li><p>Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed</p></li><li><p>Participate in department working groups, contributing to tool development and process improvement</p></li><li><p>Design and test program logic independently, maintaining documentation in a regulated environment</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Enjoy working independently while staying closely connected to a broader study team</p></li><li><p>Communicate clearly and proactively, especially around shifting timelines</p></li><li><p>Take pride in accuracy and consistency when documenting and maintaining code</p></li><li><p>Think analytically and enjoy solving programming and data challenges</p></li><li><p>Stay curious about process improvement and enjoy contributing ideas to working groups</p></li><li><p>Adapt comfortably to ad hoc requests and evolving priorities from senior leadership</p></li><li><p>Bring attention to detail and a quality mindset to regulated work</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Master's degree with 3+ years of relevant experience</p></li><li><p>Proven programming experience supporting clinical study data and analysis deliverables</p></li><li><p>Strong documentation and quality control skills within a regulated environment</p></li><li><p>Experience collaborating within a multidisciplinary study team</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager QA Auditor GCP Strategy]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48491]]></requisitionid>
    <referencenumber><![CDATA[R48491]]></referencenumber>
    <apijobid><![CDATA[r48491]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48491/senior-manager-qa-auditor-gcp-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong></p></div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Audit Strategy, Global Development to join our Global Development Quality Assurance (GDQA), supporting our Global Development organization in a remote work mode. In this role, you will lead risk-based audit strategy programs and oversee compliance across therapeutic areas, studies, and audit activities while collaborating with Global Development teams, auditors, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p></div><div><p><strong>When & where: </strong></p></div><div><p>UK Remote - Ireland Remote </p></div><div><p><strong>Discover your role: </strong></p></div><div><ul><li><p>Lead risk-based audit planning across therapeutic areas and studies </p></li><li><p>Drive strategic audit programs using risk indicators from study teams </p></li><li><p>Ensure audits align with approved programs and scheduled timelines </p></li><li><p>Manage audit outcomes to identify trends and communicate risks </p></li><li><p>Represent quality assurance on complex cross-functional initiatives </p></li><li><p>Deliver reports and metrics to Global Development leadership </p></li><li><p>You collaborate effectively with stakeholders across global functions </p></li><li><p>You navigate ambiguity while prioritizing multiple complex activities </p></li><li><p>10-20% travel might be required </p></li></ul></div><div></div><div><p>This role requires: </p></div><div><ul><li><p>Bachelor’s degree with 8+ years of relevant industry experience </p></li></ul></div><div><ul><li><p>5+ years of GCP audit strategy or audit experience </p></li></ul></div><div><ul><li><p>Knowledge of FDA, EU, and ICH GCP regulations and guidance </p></li></ul></div><div><ul><li><p>Experience supporting or participating in regulatory inspections </p></li></ul></div><div><ul><li><p>Strong project management and stakeholder management capabilities </p></li></ul></div><div><ul><li><p>Excellent written and verbal communication skills with senior audiences </p></li></ul></div></div><div></div><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49505]]></requisitionid>
    <referencenumber><![CDATA[R49505]]></referencenumber>
    <apijobid><![CDATA[r49505]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49505/associate-manager-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate</strong> <strong>Manager</strong> to join our <strong>Regulatory Affairs Strategy (Oncology) </strong>team.</p><p>The Associate Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Coordinating the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development in oncology therapeutic area, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure</p></li><li><p>Assisting in coordination and preparation for Agency meetings and associated briefing document preparation</p></li><li><p>Managing and tracking queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments</p></li><li><p>Providing representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings</p></li><li><p>Performing research to support the development of regulatory strategy for the assigned clinical development program</p></li><li><p>Maintaining knowledge of regulatory requirements up to current date, comments on draft regulatory guidance, and communicates changes in regulatory information as needed</p></li><li><p>Exercising discretion and independent judgment in the performance of the duties described above</p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum MD, PhD or PharmD degree along with relevant internship, fellowship, post-doc experience or industry experience</p></li><li><p>Experience in oncology preferred</p></li><li><p>Knowledgeable of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices.</p></li><li><p>Experience interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred</p></li><li><p>High attention to detail; ability to organize and prioritize assigned projects according to corporate goals</p></li><li><p>Ability to work in close collaboration with colleagues in regulatory department and throughout the development organization</p></li><li><p>Proficient in written, oral, and interpersonal communications in English</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, Clinical Data Reporting]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48589]]></requisitionid>
    <referencenumber><![CDATA[R48589]]></referencenumber>
    <apijobid><![CDATA[r48589]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48589/specialist-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><div><div><div><div><div><div><div><div><div><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist, Clinical Data Reporting to join our Data Management team, supporting clinical trial oversight and study-level data review in a hybrid role. In this role, you will produce accurate and consistent reporting outputs that drive data cleaning, medical review, and operational decision-making, while collaborating with clinical data management, technology partners, and cross-functional teams to deliver study-level reports on schedule. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Program and maintain standardized clinical data reports and listings used for participant-level data review, data cleaning, and operational oversight</p></li><li><p>Translate study reporting requirements into technical specifications and implement outputs using established frameworks and data standards</p></li><li><p>Build and validate data review listings, exception reports, reconciliation outputs between EDC and external data, and operational performance reports</p></li><li><p>You communicate clearly with cross-functional partners to clarify reporting needs and deliver outputs on schedule</p></li><li><p>Partner with clinical data management and technology teams to leverage data sources including the Scientific Data Lake, EDC systems, and external data streams</p></li><li><p>Monitor routine data refreshes, troubleshoot issues with accuracy, completeness, and integration, and contribute to automation and workflow streamlining</p></li><li><p>Keep reporting documentation, specifications, and outputs audit- and inspection-ready in line with GCP, ICH, GDPR, SOPs, and internal quality standards</p></li><li><p>You stay curious about reporting tools and methodologies, sharing knowledge of standards and processes to support team learning and continuous improvement</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's or Master's degree in Data Science, Computer Science, Life Sciences, or a related field</p></li><li><p>2+ years of experience in clinical data, data visualization, or related disciplines, with a background in building interactive reporting solutions, KPIs, and metrics to support clinical trial oversight</p></li><li><p>Proficiency in EDC systems (e.g., Medidata RAVE) and analytics, reporting, and data visualization tools such as SAS, R, Python, JReview, elluminate, Tableau, Power BI, or Spotfire</p></li><li><p>Strong understanding of clinical trial processes, clinical data standards (e.g., CDISC), and regulatory requirements (GCP, GDPR, HIPAA)</p></li><li><p>Experience with risk-based data review concepts, data quality standards, and data lifecycle management in a regulated environment</p></li><li><p>Experience with data lakes, data pipelines, data integration, automation, and reporting and analytics in a clinical research environment</p></li></ul></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Rhinology *Tokyo Area]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50002]]></requisitionid>
    <referencenumber><![CDATA[R50002]]></referencenumber>
    <apijobid><![CDATA[r50002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50002/medical-representative-mr-rhinology-startokyo-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative Immunology Commercial Japan Region to join our Immunology Commercial Team, supporting our Japan business in a hybrid work model. In this role, you will achieve immunology sales objectives while collaborating with alliance partners and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Work model: Field</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Achieve immunology sales objectives through territory budget and expense management.</li><li>Develop annual territory business plans using market insights and brand strategies.</li><li>Use key data sources to build territory action plans.</li><li>Deliver customer value through strategic engagement and tailored solutions.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Operate within regulatory, legal, and compliance requirements.</li><li>Collaborate with alliance partners to deliver shared business objectives.</li><li>You build strong customer relationships while managing priorities effectively.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree or equivalent experience.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>MR Certification and a valid driver license.</li><li>Strong customer engagement skills with a value-focused approach.</li><li>Ability to conduct disease and concept-based selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and independent execution skills.</li><li>Computer proficiency with word processing, spreadsheets, databases, and email software.</li><li>Ability to tailor presentations to different audiences.</li><li>Alliance experience or exposure.</li><li>Therapy area knowledge in rhinology and respiratory preferred.</li><li>Biologics sales experience preferred.</li><li>Current clinical knowledge of therapy areas and competitor brands preferred.</li><li>Established key opinion leader relationships in rhinology and respiratory preferred.</li><li>English fluency is a plus.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44959]]></requisitionid>
    <referencenumber><![CDATA[R44959]]></referencenumber>
    <apijobid><![CDATA[r44959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44959/senior-manager-global-patient-safety-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager</strong> to join our <strong>Patient Safety</strong> team.The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Complete signal detection activities in line with approved safety surveillance plan</p></li><li><p>Perform signal evaluation for any identified signals and author the safety evaluation reports</p></li><li><p>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</p></li><li><p>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned compounds</p></li><li><p>Participate in other risk management activities as appropriate for assigned compounds</p></li><li><p>We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron</p></li><li><p>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</p></li></ul><p><strong>This role requires:</strong>​</p><ul><li><p>Minimum a Master's, PhD, or PharmD</p></li><li><p>Offers 7+ years of relevant risk management experience in the pharmaceutical/ biotech industry or health authority</p></li><li><p>Ability to apply relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments</p></li><li><p>Ability to work with a safety system database for purposes of medical case review and simple queries</p></li><li><p>Able to be proactive and self-disciplined, you can meet deliverables, and effectively use your time and prioritize</p></li><li><p>Ability to effectively communicate (verbal and written) safety findings</p></li></ul><p>#GDPSJobs </p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Science Liaison Hematology (f/m/d) - Germany North-West]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49869]]></requisitionid>
    <referencenumber><![CDATA[R49869]]></referencenumber>
    <apijobid><![CDATA[r49869]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49869/medical-science-liaison-hematology-fmd-germany-north-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Field Medical Affairs Hematology / MSL (f/m/d) to join our Medical Affairs team, supporting North-West Germany in a field-based work model. In this role, you will drive scientific exchange, generate medical insights, and advance research initiatives while collaborating with Medical Affairs, Clinical Development, Market Access, Commercial, and healthcare experts. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Field-based in North-West Germany</p><p><strong>Discover your role:</strong></p><ul><li><p>Build and maintain relationships with key opinion leaders in hematologic malignancies.</p></li><li><p>Generate strategic medical insights to inform cross-functional decision-making.</p></li><li><p>Serve as the primary scientific resource for healthcare professionals across the territory.</p></li><li><p>Support Medical Affairs, Marketing, and Market Access projects and programs.</p></li><li><p>Contribute to company-sponsored studies through investigator and site engagement.</p></li><li><p>Present scientific, clinical, and disease-state data in a compliant manner.</p></li><li><p>Collect and report scientific, clinical, and competitive intelligence at congresses.</p></li><li><p>You adapt to evolving field needs while building trusted scientific partnerships.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD, PharmD, MD, DVM, or equivalent doctoral degree with 4+ years' relevant experience, including 2+ years as a Medical Science Liaison in hematology or oncology; or Master's degree with 6+ years' relevant experience, including 3+ years as a Medical Science Liaison.</p></li><li><p>Knowledge or experience in hematology; multiple myeloma and/or lymphoma experience preferred.</p></li><li><p>Knowledge of treatment guidelines, clinical research processes, European Union regulations, and compliant pharmaceutical practices.</p></li><li><p>Experience engaging healthcare experts and institutions focused on hematologic malignancies preferred.</p></li><li><p>Drug launch experience preferred.</p></li><li><p>Ability to communicate complex scientific data and operate as a scientific peer.</p></li><li><p>Experience in cross-functional matrix organizations, including collaboration with commercial partners.</p></li><li><p>Strong written and verbal communication, strategic conversation, planning, prioritization, and problem-solving skills.</p></li><li><p>Ability to work independently while maintaining compliance with regulatory requirements.</p></li><li><p>Proficiency with word processing, presentation, and spreadsheet applications.</p></li><li><p>Valid driver's license, clean driving record, and ability to travel up to 70%, including overnight and occasional weekend travel.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>92.250,00 € - 153.750,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager - Hematology (f/m/d) - Germany South-West]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49849]]></requisitionid>
    <referencenumber><![CDATA[R49849]]></referencenumber>
    <apijobid><![CDATA[r49849]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49849/key-account-manager-hematology-fmd-germany-south-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hematology to join our International Hematology team, supporting Germany in a field-based work mode. In this role, you will drive account performance and regional contracting activities for our hematology portfolio while collaborating with Medical colleagues, pharmacists, hospital stakeholders, and commercial teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Field-based in Germany South-West</p><p><strong>Discover your role:</strong></p><ul><li><p>Establish high-quality healthcare professional relationships across the territory</p></li><li><p>Develop referral networks spanning hospital, outpatient, and office-based settings</p></li><li><p>Deliver portfolio value messages through face-to-face, remote, and digital engagement</p></li><li><p>Partner with Medical on regional programs and healthcare professional activities</p></li><li><p>Manage account planning, segmentation, targeting, and local account plans</p></li><li><p>Support regional contracting activities and adapt contract models to local needs</p></li><li><p>Analyze market trends and competitor activity to inform negotiations</p></li><li><p>Thrive in an agile environment and adjust priorities to account needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or recognized equivalent for sales professionals</p></li><li><p>5-7 years of progressive pharmaceutical or biotechnology sales experience</p></li><li><p>Knowledge of the German healthcare system and regional market structures</p></li><li><p>Experience using data, customer relationship management systems, and multiple business systems</p></li><li><p>Qualification in applicable pharmaceutical industry codes, including EFPIA Code or VFA Pharmakodex</p></li><li><p>Fluency in German and good working knowledge of English</p></li><li><p>Ability to manage a large territory independently with frequent travel</p></li><li><p>Strong customer engagement, negotiation, and communication skills</p></li><li><p>High integrity and ethical standards in all interactions</p></li><li><p>Hematology sales experience and an established network strongly preferred</p></li><li><p>Experience supporting hospital, purchasing group, or payer contract negotiations preferred</p></li><li><p>Product launch experience preferred</p></li></ul><p>Salary range (annually)</p><p>73,125 -121,875 €</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Management Process, Quality & Inspection Readiness]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48439]]></requisitionid>
    <referencenumber><![CDATA[R48439]]></referencenumber>
    <apijobid><![CDATA[r48439]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48439/director-data-management-process-quality-inspection-readiness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Director, Data Management Process, Quality, and Inspection Readiness provides strategic leadership for Data Management quality, inspection readiness, and process excellence. This role is accountable for establishing and driving standardized approaches to Data Management quality, process frameworks, governance, compliance, and operational execution while ensuring compliance with global regulatory requirements, GCP, and industry best practices. The position serves as the primary Data Management lead for health authority inspections and audits, accountable for inspection preparation, response coordination, functional representation, and ensuring teams are prepared to effectively represent the function during regulatory inspections. In addition, the role also owns and drives the development, governance, and continuous improvement of Data Management processes, training programs, and operational frameworks to support standardized, scalable, compliant, and inspection-ready execution across the Data Management organization. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Warren, NJ, Tarrytown, NY or Armonk, NY</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Data Management Quality and Inspection Readiness</em></p><ul><li><p>Provide strategic leadership for Data Management quality and compliance, ensuring consistent application of quality standards and resolution of complex and systemic issues.</p></li><li><p>Develop Data Management quality frameworks, including CRO oversight, issue management, escalation pathways, and quality oversight processes to support proactive identification and management of operational quality issues and compliance gaps.</p></li><li><p>Ensure Data Management quality frameworks and operational activities are aligned with GCP, ICH guidelines, global regulatory requirements, and company quality standards.</p></li><li><p>Lead quality event and CAPA management activities, including root cause analysis, and implementation of sustainable corrective and preventive actions. Leverage insights to strengthen controls, improve processes, and enhance inspection readiness.</p></li><li><p>Collaborate with CRO partners and internal stakeholders on quality events, issue escalation, remediation activities, and CAPA implementation.</p></li><li><p>Lead Data Management inspection readiness and audit support; direct preparation, coordination, and response for health authority inspections.</p></li><li><p>Lead and conduct independent, risk-based reviews of study documentation and operational conduct at defined and ad hoc timepoints to identify gaps, strengthen compliance, and ensure sustained inspection readiness.</p></li><li><p>Establish Data Management quality review processes to identify process gaps and deficiencies, training needs, and the documentation of risks, enabling early remediation.</p></li><li><p>Establish and leverage Data Management KPI & KQI frameworks to provide visibility into performance, data quality, & compliance trends, driving proactive decision-making, continuous improvement, & innovation across the portfolio.</p></li><li><p>Define, monitor, and perform effectiveness checks measures for Data Management quality, compliance, inspection readiness, training and process performance to drive continuous improvement and operational excellence.</p></li><li><p>Lead impact assessments for new and evolving regulatory requirements, ensuring appropriate updates to Data Management processes, quality standards, and operational practices.</p></li><li><p>Educate and guide the Data Management organization on quality standards, regulatory expectations, and inspection readiness practices.</p></li><li><p>Establish and maintain strong partnerships with Inspection Management and Quality stakeholders to ensure alignment on inspection readiness activities, quality standards, compliance expectations, and remediation strategies.</p></li><li><p>Oversee Data Management SharePoint repositories to support centralized access to current quality and inspection readiness documentation.</p></li></ul><p><em>Data Management Process and Training</em></p><ul><li><p>Own and drive the development, governance, and continuous improvement of Data Management processes to support scalable, standardized, compliant, and inspection-ready execution.</p></li><li><p>Develop and execute robust implementation and change management plans for new and revised Data Management processes to ensure consistent adoption, operational effectiveness, and sustainable execution.</p></li><li><p>Establish & maintain training frameworks to support consistent implementation through development, maintenance, and delivery of role-based training and guidance.</p></li><li><p>Lead the Data Management SME network to ensure designated subject matter expertise, process ownership, and functional support coverage across Data Management.</p></li><li><p>Oversee Data Management SharePoint repositories to support centralized access to current process and training documentation.</p></li><li><p>Serve as a Data Management representative in the Global Development Process Owner Network.</p></li><li><p>Establish and maintain strong partnerships with the Process & Procedures, Learning Center of Excellence, Change Management functions to ensure alignment on Data Management processes and training.</p></li><li><p>Lead and contribute to cross-functional process improvement initiatives as required.</p></li></ul><p><em>People Management</em></p><ul><li><p>Responsible for line management and performance of direct reports, including the development of competencies, coaching, and assessment of annual performance.</p></li><li><p>Provide leadership, mentorship, and guidance to direct reports, fostering skill development, knowledge sharing, and operational excellence.</p></li><li><p>Foster a culture of accountability, collaboration, continuous improvement, and quality.</p></li><li><p>Support prioritization and workload management to ensure effective utilization.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum Bachelor's Degree (Science, Health, Computing, or related field) with 12+ years in Clinical Data Management within the biotechnology, pharmaceutical or health related industry.</p></li><li><p>5+ years of people management, leadership, and mentoring</p></li><li><p>Expert knowledge of clinical data management principles, processes, quality frameworks, and inspection readiness practices within a global clinical development environment.</p></li><li><p>Deep understanding of global regulatory requirements and industry standards, including GCP, ICH guidelines, 21 CFR Part 11, ALCOA+ principles and inspection readiness expectations.</p></li><li><p>Demonstrated experience leading Data Management quality, compliance, inspection readiness, audit support and process governance activities.</p></li><li><p>Demonstrated experience developing, implementing, and continuously improving departmental processes, quality standards and frameworks, and operational controls.</p></li><li><p>Strong knowledge of quality management systems, CAPA processes, issue management, escalation frameworks, and continuous improvement methodologies.</p></li><li><p>Demonstrated experience supporting multiple health authority inspections across different health authorities (e.g., FDA, PMDA, MHRA, EMA, etc..) including inspection preparation, response coordination, remediation activities, and functional representation during regulatory inspections.</p></li><li><p>Experience establishing and leveraging KQI / KPI frameworks, effectiveness measures, and operational metrics to drive quality oversight, compliance monitoring, and process improvement.</p></li><li><p>Demonstrated ability to lead organizational change management initiatives, including implementation of new processes, quality standards, and operational frameworks.</p></li><li><p>Demonstrated success in solving complex business problems through strategic and critical thinking.</p></li><li><p>Proven ability to lead and influence within a matrix organization, driving alignment and outcomes with cross-functional stakeholders without direct authority</p></li><li><p>Proven ability to build strong collaborative relationships and influence alignment across key internal and external stakeholders.</p></li><li><p>Strong understanding of cross-functional activities and management of multiple and varied tasks with enthusiasm and attention to detail.</p></li><li><p>Excellent interpersonal, oral, and written communication skills.</p></li><li><p>Demonstrated ability to effectively lead and prioritize within a fast-paced, evolving, and highly regulated environment.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Non-Viral Delivery Tech (Chromatography)]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47529]]></requisitionid>
    <referencenumber><![CDATA[R47529]]></referencenumber>
    <apijobid><![CDATA[r47529]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47529/associate-scientist-non-viral-delivery-tech-chromatography/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist to join our Non-Viral Delivery Technologies group within Regeneron Genetic Medicines. In this role, you will support production, purification, and characterization of protein reagents used in next-generation delivery technology development, helping to expand the company's growing genetic medicines portfolio while collaborating with team members and groups across the company.This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Maintain and manipulate suspension cells</p></li><li><p>Operate AKTA systems for small-scale purification using liquid chromatography-based techniques (e.g., affinity, ion exchange, size exclusion)</p></li><li><p>Develop high-throughput protein purification and conjugation workflows</p></li><li><p>Characterize purified proteins using methods such as SDS-PAGE, SE-UPLC, and CE</p></li><li><p>Manage and organize data and workflows with strong attention to detail</p></li><li><p>Troubleshoot logistical and technical hurdles as they arise</p></li><li><p>Work independently and show initiative to continually improve protocols and processes</p></li><li><p>Thrive in a fast-paced, highly collaborative environment</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/MS in molecular biology, biochemistry, bioengineering, or a related field</p></li><li><p>Strong collaboration skills, attention to detail, and organizational ability</p></li><li><p>Preferred: experience with aseptic technique in mammalian cell culture, chromatography, running an AKTA Pure/Avant, and SDS-PAGE/CE</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Ophthalmology]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48582]]></requisitionid>
    <referencenumber><![CDATA[R48582]]></referencenumber>
    <apijobid><![CDATA[r48582]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48582/associate-director-clinical-scientist-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting Ophthalmology. In this role, you will contribute to the development, evaluation, planning and execution of Internal Medicine clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Work in a matrix environment as part of a cross-functional team (with internal and external vendor representation) and may contribute to candidate development projects through early and/or late phase development. You will report to the Sr Dir/Director, Clinical Science, Internal Medicine and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p><strong>Location: </strong>Tarrytown, NY, Warren, NJ, Cambridge, MA</p><h3><strong>Discover your role:</strong></h3><ul><li><p>May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Contributes to planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc)</p></li><li><p>≥ 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Ophthalmology</p></li><li><p>Proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills</p></li><li><p>Experience in all aspects of conducting global clinical trials and execution of clinical programs</p></li><li><p>We need an individual who is a strong team-player; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -OAKLAND, CA / SACRAMENTO, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48075]]></requisitionid>
    <referencenumber><![CDATA[R48075]]></referencenumber>
    <apijobid><![CDATA[r48075]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48075/medical-account-specialist-ii-neurology-oakland-ca-sacramento-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Oakland]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Oakland (Metro), CA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist: Bispecifics and Antibody Engineering]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47480]]></requisitionid>
    <referencenumber><![CDATA[R47480]]></referencenumber>
    <apijobid><![CDATA[r47480]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47480/senior-scientist-bispecifics-and-antibody-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a results-driven Senior Scientist to join Regeneron’s Antibody Engineering team within the Bispecifics and Antibody Engineering Department. In this fast-paced, innovative group, you will design, produce, and characterize next-generation antibody and protein therapeutics across multiple therapeutic areas with a focus on myeloid cell biology. Your work will directly contribute to the pipeline and help build new platform capabilities at a pivotal time for antibody engineering.</p><p><strong> </strong></p><p><strong>As a Senior Scientist, a typical day could require the following:</strong></p><ul><li><p>Apply molecular and structural biology expertise to independently design innovative multi-specific antibodies with desired potency, selectivity and developability.</p></li><li><p>Perform molecular and structural-guided design, high-throughput construct generation, and vector engineering using modern software and tools.</p></li><li><p>Produce and purify novel and logic-gated alternative format antibodies using mammalian expression systems utilizing an assortment of molecular biology & biochemical techniques (i.e. AKTA systems and other chromatographic columns).</p></li><li><p>Characterize binding affinities, binding kinetics & stability. </p></li><li><p>Design and implement high-throughput and properly controlled biochemical and cell-based assays (ELISA and AlphaLISA, flow cytometry binding, phagocytic assays, cell activation and cytolytic assays).</p></li><li><p>Troubleshoot bioanalytical and cell-based assay data to inform subsequent iterations.</p></li><li><p>Engage program stakeholders to communicate biologic designs with data updates to meet program objectives. </p></li></ul><ul><li><p>Clearly convey results to management during cross-departmental meetings and maintain timely, accurate entries using Benchling and research ELN.</p></li></ul><p><strong>This role may be a strong fit If You:</strong></p><ul><li><p>Have expertise in myeloid, molecular, and protein biology.</p></li><li><p>Learn new skills quickly and troubleshoot antibody production and functional assays effectively.</p></li><li><p>Excel in data analysis and interpretation while supporting multiple projects simultaneously.</p></li><li><p>Competently prioritize efforts to quickly adapt to evolving program directions.</p></li><li><p>Possess exemplary organizational, communication, and presentation skills.</p></li><li><p>Enjoy collaborating across diverse, cross-functional teams. </p></li></ul><p><strong>To be considered for this role you must have </strong>a PhD in molecular biology, cell biology, biochemistry, immunology or a related field with at least one year of relevant experience in academia or industry. Core hands-on experience with cloning, antibody expression in mammalian cell lines, antibody purification (i.e., using AKTA systems), and comprehensive protein characterization is desired; however, we’re excited to train motivated learners. Familiarity with cell-free expression and structural AI/ML-design is preferred but not required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology-Seattle, WA]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49995]]></requisitionid>
    <referencenumber><![CDATA[R49995]]></referencenumber>
    <apijobid><![CDATA[r49995]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49995/medical-specialist-ii-ophthalmology-seattle-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p>The Medical Specialist will report to the Regional Director, and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Seattle, WA</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Experience in biologics and buy and bill products</p></li><li><p>Demonstrated history of high sales performance</p></li><li><p>Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p></li></ul><p><strong>This role requires:</strong></p><ul><li>A Bachelor's degree is required and a degree in science or business is preferred (master’s degree a plus)</li><li>A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Buy and Bill experience</li><li>Ophthalmology with relevant retina experience is preferred.</li><li>Must be based in or located in close proximity to the assigned territory (relocation will not be provided). Ability to travel (40-60%).</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 10:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Hearing Loss and Vestibular Disorders]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50090]]></requisitionid>
    <referencenumber><![CDATA[R50090]]></referencenumber>
    <apijobid><![CDATA[r50090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50090/principal-scientist-hearing-loss-and-vestibular-disorders/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Scientist to join our team developing therapies for hearing loss and vestibular disorders. In this role, you will independently lead research projects and drive the development of novel therapies for inner ear disorders, while collaborating with a cross-functional team to advance translationally relevant studies.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul></li></ul><p><strong>Discover your role:</strong></p><ul><li><ul><li><p>Lead the design of rigorous experiments to address core questions in hearing biology that drive drug discovery and preclinical programs</p></li><li><p>Develop and characterize novel animal models to understand mechanisms of hearing loss and evaluate novel therapeutics</p></li><li><p>Design and execute in vivo and in vitro functional assays to understand syndromic and non-syndromic hearing loss</p></li><li><p>Work cross-functionally with a team to develop translationally relevant studies</p></li><li><p>Analyze and evaluate data with rigor, presenting findings internally and externally</p></li><li><p>Draft and review protocols and articles for publication independently</p></li><li><p>Motivate, develop, and supervise junior scientists, research associates, and other trainees</p></li><li><p>Thrive in a dynamic, fast-paced environment, adapting readily to shifting priorities</p></li></ul></li></ul><p><strong>This role requires:</strong></p><ul><li><ul><li><p>Ph.D. with a strong record of innovation and publication, plus 5+ years of relevant experience</p></li><li><p>Proven expertise in drug development</p></li><li><p>Strong ability to work both independently and in a team, communicating effectively across all levels</p></li><li><p>Resilience in overcoming challenges and a rigorous approach to scientific work</p></li><li><p>Preferred: managerial experience</p></li><li><p>Preferred: in vivo experimental experience</p></li><li><p>Preferred: strong understanding of human and mouse genetics and/or auditory physiology</p></li></ul></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Regulatory Affairs]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50067]]></requisitionid>
    <referencenumber><![CDATA[R50067]]></referencenumber>
    <apijobid><![CDATA[r50067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50067/senior-manager-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Regulatory Strategy Oncology & Japan Affairs to join our Regulatory Affairs team, supporting our Japan business in a hybrid work model. In this role, you will lead Japan regulatory strategies across multiple therapeutic areas while collaborating with global regulatory teams and local cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Japan</p><p>Work model: Hybrid</p><br><p><strong>Discover your role:</strong></p><p>• Plan and execute Japan regulatory strategies and PMDA consultations for assigned programs<br>• Lead marketing application and post-approval change submissions<br>• Partner with local and global leadership to support Regulatory Affairs operations<br>• Manage interactions with PMDA and other Japanese health authorities<br>• Lead or support clinical trial notification preparation and submission activities<br>• Represent Regulatory Affairs within clinical, commercial, medical, and patient safety teams<br>• Support local labeling, patient information, and promotional material review activities<br>• You build strong partnerships across a global matrix environment</p><br><p><strong>This role requires:</strong></p><p>• Bachelor's degree in a scientific discipline; Master's degree preferred<br>• 10+ years in the pharmaceutical industry and 5+ years of relevant regulatory experience<br>• Experience managing health authority interactions, major submissions, and approvals in Japan<br>• Deep knowledge of Japan submission requirements, local regulations, and regulatory standards<br>• Knowledge of clinical trial requirements and ability to resolve local procedural challenges<br>• Experience supporting business start-up activities<br>• Ability to ensure compliance with Japan regulatory requirements and local standards<br>• Strategic thinking, commercial awareness, and strong written and verbal communication skills<br>• Ability to thrive in and foster effective matrix teamwork in a global environment<br>• Fluent Japanese and English language skills</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Field Reimbursement Manager  - Neurology (West)]]></title>
    <date><![CDATA[Fri, 21 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48128]]></requisitionid>
    <referencenumber><![CDATA[R48128]]></referencenumber>
    <apijobid><![CDATA[r48128]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48128/senior-field-reimbursement-manager-neurology-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Los Angeles, (Metro) CA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45872]]></requisitionid>
    <referencenumber><![CDATA[R45872]]></referencenumber>
    <apijobid><![CDATA[r45872]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45872/principal-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Principal Analytical Sciences Scientist to support Manufacturing, Process Sciences (PS), and Quality Control (QC) by developing, optimizing, troubleshooting, validating, transferring, and applying analytical procedures across multiple modalities, including iSRNA/siRNA oligonucleotides and peptide therapeutics. You will advance QC capabilities by creating robust, phase‑appropriate and lifecycle‑managed analytical methods, integrating new assays and technologies, and serving as a technical leader who resolves complex issues and elevates analytical strategy for novel modalities.</p><p><strong>When & Where:</strong></p><p><strong>Location: Rensselaer, NY</strong></p><p><strong>Work Model: Monday-Friday 8am-4:30pm</strong></p><p><strong>Discover Your Role:</strong></p><ul><li>Establish, develop, and optimize analytical methods for product and raw materials, with a focus on iSRNA/siRNA and peptide modalities.</li><li>Design and review protocols for assay qualification and validation (e.g., ICH Q2 principles), ensuring methods are stability‑indicating and suitable for GMP release and characterization.</li><li>Engage with collaborators and vendors to identify, assess, and implement new instrumentation and technology (e.g., LC‑MS, CE, ion‑pair RP‑HPLC, hybridization‑based assays, peptide mapping).</li><li>Transfer control test procedures to QC and other relevant departments, including drafting transfer plans, training materials, and acceptance criteria.</li><li>Lead troubleshooting and provide analytical support for established test methods, process, and formulation issues (e.g., nuclease sensitivity in iSRNA, peptide oxidation/deamidation).</li><li>Conduct investigations (OOS/OOT), support deviation root‑cause analysis, and lead customer complaint assessments with data‑driven conclusions.</li><li>Present findings and scientific arguments in meetings and technical reports; communicate risk, impact, and mitigation strategies clearly.</li><li>Train and mentor junior team members; author and revise SOPs, protocols, and method lifecycle documents.</li><li>Manage the lifecycle of analytical testing methods (development, validation, transfer, change control, periodic review, and retirement).</li><li>Design and execute experiments independently to assess and optimize technologies; apply DOE and statistical trending where appropriate.</li><li>Produce and maintain accurate, compliant records consistent with data integrity and cGMP expectations.</li><li>Represent Analytical Sciences on interdepartmental teams and in program meetings; align analytical strategy with CMC and regulatory milestones.</li><li>Demonstrated experience developing and validating analytical methods for iSRNA/siRNA oligonucleotides and peptide therapeutics.</li><li>Hands‑on proficiency with LC‑MS/MS, CE, ion‑pair RP‑HPLC, peptide mapping, and oligonucleotide characterization assays.</li><li>Proven track record of method transfer to QC, troubleshooting, OOS/OOT investigations, and cross‑functional collaboration.</li><li>Strong technical writing, data integrity practices, and presentation skills; ability to mentor and lead.</li></ul><p><strong>This Role Requires:</strong></p><p>A PhD in Chemistry, Biochemistry, Biology, or related field, with 3+ years of relevant industry experience in analytical development and QC method lifecycle.</p><ul><li>Level determined based on qualifications.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director - Data Management, Analytics, AI & Architecture]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50015]]></requisitionid>
    <referencenumber><![CDATA[R50015]]></referencenumber>
    <apijobid><![CDATA[r50015]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50015/executive-director-data-management-analytics-ai-architecture/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is a leading biotechnology company built on a simple but powerful mission: to use the power of science to bring new medicines to patients, over and over again. Founded and led by physician-scientists, we've turned that mission into one of the industry's most productive pipelines, nearly all of it homegrown in our own laboratories, powered by proprietary technologies like our VelociSuite® platform. From Dupixent and EYLEA to a rapidly expanding portfolio across oncology, cardiovascular and metabolic disease, neuroscience, and rare disease, our science is reaching millions of patients worldwide, and we're just getting started.</p><p>As we invest billions in new manufacturing capacity, expand our global footprint, and build the next generation of digital and technology capabilities to match the scale of our ambition, Regeneron offers a rare combination: the resources and reach of an industry leader, paired with the energy, curiosity, and relentless focus on invention of a company still writing its next chapter. This is a place where technology doesn't just support the business, it accelerates the science that changes patients' lives.</p><p><em>This role will sit on-site in our Sleepy Hollow, NY offices 4 days per week.</em></p><p><strong>Role Description</strong></p><div>The Executive Director of Data Management, Analytics, and Architecture will lead the strategy for commercial and G&A data capabilities at Regeneron, transforming enterprise data into trusted insights that drive business performance and operational excellence. This role partners closely with Digital & Technology leaders and senior executives to establish scalable data architecture, analytics, and governance standards that serve as a model across the organization.</div><div></div><div>The position has significant influence over how data, AI, and analytics are structured, managed, and leveraged to support commercial and operational decision-making. The leader also serves as the primary executive spokesperson for data management, analytics, and architecture across Commercial and G&A functions, including Finance, HR, Procurement, Legal, Compliance, and other corporate departments.</div><p><strong>What You'll Lead</strong></p><ul><li>Own and execute the multi-year data management, analytics, AI, and enterprise data architecture strategy for Commercial and G&A functions, aligning investments with corporate objectives.</li><li>Lead and develop a high-performing team of data management, analytics, and architecture professionals, building organizational capability and delivery excellence.</li><li>Deliver trusted data platforms, analytics products, and self-service capabilities that empower business leaders across Commercial, Finance, HR, and other G&A functions.</li><li>Establish enterprise-wide data governance, stewardship, quality, lifecycle management, and master data standards to improve trust, consistency, and interoperability.</li><li>Modernize and simplify the data ecosystem through scalable cloud platforms, integration strategies, architecture standards, and executive reporting capabilities.</li><li>Advance AI, machine learning, automation, and responsible AI practices by identifying high-value use cases, managing risk, and ensuring regulatory compliance.</li><li>Drive measurable business outcomes through improved data quality, analytics adoption, automation, operational efficiency, productivity, and process standardization across global teams.</li><li>Oversee vendor partnerships, data security, architecture governance, and value realization, ensuring strategic investments deliver measurable business impact and long-term organizational value.</li></ul><p><strong>What You Bring</strong></p><ul><li>BS/BA in Computer Science, Data Science, Information Systems, or a related field required; MS. PhD or MBA preferred.</li><li>17+ years of progressive leadership in data management, data architecture, analytics, or business intelligence, including enterprise-scale programs; experience in life sciences, biotechnology, or another regulated industry is a plus.</li><li>Deep command of modern data management, analytics, and enterprise architecture capabilities (platform-agnostic, e.g., BI, cloud data platforms, data governance, data modeling, master data management).</li><li>Experience establishing enterprise data governance frameworks and reference architecture standards that scale across multiple business domains.</li><li>Strong understanding of AI, machine learning, and agentic AI concepts, including model risk, responsible AI practices, and the operational discipline, such as monitoring, validation, and lifecycle management, needed to run AI systems safely at enterprise scale.</li><li>Familiarity with regulatory and risk frameworks relevant to AI and data in regulated industries (e.g., GxP considerations, NIST AI RMF, ISO 42001) is a plus.</li><li>Experience partnering with Legal, Compliance, Security, and Privacy functions to manage data and AI risk, vendor risk, and audit readiness.</li><li>Proven ability to influence senior leaders, translate data into business outcomes, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50213]]></requisitionid>
    <referencenumber><![CDATA[R50213]]></referencenumber>
    <apijobid><![CDATA[r50213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50213/reimbursement-business-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><h3>When & where:</h3><ul><li>Greater Dallas, TX area</li><li>In the field 4 days a week</li></ul><h3>Discover your role:</h3><ul><li>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</li><li>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</li><li>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li><li>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</li><li>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</li></ul><h3>This role requires:</h3><ul><li>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience.</li><li>Experience working with products delivered through a Specialty Pharmacy network is essential.</li><li>Collaboration and proactive communication skills required.</li><li>Background in leadership and effective cross functional partnership a plus.</li><li>Established ability to work within an Account Management based structure.</li><li>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</li><li>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Preclinical & Translational PK/PD]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47275]]></requisitionid>
    <referencenumber><![CDATA[R47275]]></referencenumber>
    <apijobid><![CDATA[r47275]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47275/associate-director-preclinical-translational-pkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of Translational/Preclinical Modeling develops and implements quantitative and mechanistic PK/PD models to aid in the understanding of target biology, therapeutic modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic direction of modeling and simulation sciences.</p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Independently develops and implements quantitative and mechanistic mathematical PK/PD models that inform preclinical-to-early clinical translation, including human efficacious dose predictions and first-in-human dose selection.</p></li><li><p>Actively contributes to the advancement and strategic direction of modeling and simulation sciences</p></li><li><p>Provides expert support to pre-clinical PK/PD project representatives and R&D project teams to design, execute and interpret in vitro and in vivo quantitative pharmacology studies. This included working with the Research PK group to optimize use of mouse PK data to inform translation to nonhuman primate and human PK.</p></li><li><p>Effectively integrates and summarizes modeling and simulation analyses into useable information for multidisciplinary project teams.</p></li><li><p>Remains apprised of emerging science and literature, and effectively collaborates with subject matter experts in Clinical Pharmacology, Quantitative Pharmacology and R&D to advance modeling and simulation sciences.</p></li><li><p>Presents work at internal/external scientific meetings and publishes work in scientific journals</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>Experience using one or more modeling and simulation platforms (e.g., Phoenix NLME, NONMEN, Monolix, ADAPT, MATLAB, SimBiology, etc.)</p></li><li><p>Strong theoretical and practical foundation in pharmacokinetics, including non-compartmental, compartmental, PK/PD and PBPK.</p></li><li><p> Effectively work in a fast-paced, highly-matrixed team-based environment and leverages scientific reasoning to influence key stakeholders.</p></li><li><p>Ability to learn new areas of biological sciences to develop quantitative and mechanistic PK/PD models for emerging therapeutic modalities.</p></li><li><p>Familiarity with biotherapeutic modalities, including monoclonal and bispecific antibodies, gene therapy, CAR-T, siRNAs and other targeting agents preferred</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><p>Ph.D. or M.S. in pharmacokinetics, pharmaceutical sciences, engineering, applied mathematics or related disciplines with a track record of applying quantitative and mechanism-based PK/PD modeling and simulation approaches to advance the discovery and development of therapeutics. Greater than 6 years of pharmaceutical industry or related experience in developing and applying mechanism-based PK/PD models to guide R&D teams from early discovery to IND-stage clinical development.</p><p><strong> </strong></p><p><strong> </strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - RICHMOND, VA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48017]]></requisitionid>
    <referencenumber><![CDATA[R48017]]></referencenumber>
    <apijobid><![CDATA[r48017]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48017/medical-account-specialist-ii-neurology-richmond-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Richmond (Metro), VA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Biostatistics - Genetic Medicine]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46282]]></requisitionid>
    <referencenumber><![CDATA[R46282]]></referencenumber>
    <apijobid><![CDATA[r46282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46282/associate-director-biostatistics-genetic-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development. </p><p><strong>In this role, a typical day might include:</strong> ​</p><p>The incumbent will lead efforts of the Biostatistics department with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. The incumbent will represent statistical issues in regulatory agency meetings. The incumbent will lead the development and delivery of training to non-statistical colleagues, lead the development of new infrastructure and processes, and be active in representing the company in professional associations, conferences, and publications. As an Associate Director, the incumbent will be responsible for mentoring and overseeing less experienced statisticians, with the potential to manage full-time staff. </p><p><strong>This role might be for you if can:</strong> ​</p><ul><li><p>Represent Biostatistics at Global Clinical sub-teams. </p></li><li><p>Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.</p></li><li><p>Lead contributions to the preparation of material to be used in regulatory interactions, including drafting analysis plan and reviewing TFLs to be used in regulatory meetings, slides for advisory committee meetings, etc.</p></li><li><p>Lead and contributes to process improvement and technical working groups and sets timelines and expectations for the deliverables. Authors new/revised SOPs and contributes to cross-functional EPIC workstreams. </p></li><li><p>Evaluate appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</p></li><li><p>Prepare presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management. </p></li><li><p>Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD or equivalent degree in statistics/biostatistics with >6 years of experience in the pharmaceutical industry OR MS degree in statistics/biostatistics with >11 years of experience</p></li><li><p>Preferred: Hematology, IO, non-oncology, Multiple Myeloma experience or similar Therapeutic Area.</p></li><li><p>Time to Event (TTE) experience.</p></li><li><p>Knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies.</p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Expertise in statistical software</p></li></ul><p>#GDBDMJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Corporate Counsel Transactions]]></title>
    <date><![CDATA[Mon, 29 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48785]]></requisitionid>
    <referencenumber><![CDATA[R48785]]></referencenumber>
    <apijobid><![CDATA[r48785]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48785/director-corporate-counsel-transactions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As part of the Law Department, this attorney will serve as counsel for the company in connection with licensing, business development, strategic transactions, research collaborations and services arrangements. The role is responsible for drafting, reviewing, and negotiating agreements; advising senior management on proposed transactions; and ensuring compliance with existing contractual obligations, company policy, and applicable law. The successful candidate will have proven experience in biotech, pharmaceuticals, technology or similar transactions, including structuring complex deals, advising on intellectual property matters, and managing risk across regulatory and corporate legal matters. The ideal candidate will have a history of progressive in-house or firm experience and will thrive in a highly collaborative culture.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Partner with senior management and the business development team on major corporate initiatives, including collaborations, partnerships, and licensing agreements.</p></li><li><p>Negotiate and draft sophisticated licensing, collaboration, services and other agreements, including novel structures where no precedents exist.</p></li><li><p>Support critical collaborations with the alliance management team and provide legal counsel as issues arise.</p></li><li><p>Work closely with the intellectual property department to ensure accurate protection and management of IP assets.</p></li><li><p>Advise on regulatory and legal matters affecting existing or proposed arrangements, including privacy, antitrust, securities, and corporate law.</p></li><li><p>Manage outside counsel relationships on relevant legal matters, including strategy, workstreams, and budget oversight.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>JD with strong academic credentials; BA/BS required.</p></li><li><p>Minimum 8 years of relevant experience negotiating and drafting complex agreements in the biotech, pharmaceutical, or life sciences sector.</p></li><li><p>In-house experience preferred; biotech experience strongly preferred.</p></li><li><p>Licensed to practice law in New York, or eligible for licensure as registered in-house counsel.</p></li><li><p>Please include a representative deal sheet with your application.</p></li><li><p>Deep expertise in contracts law, including drafting, negotiation, and risk analysis.</p></li><li><p>Ability to manage a high volume of client requests and competing priorities effectively.</p></li><li><p>Strong track record in business development, strategic alliances, partnerships, and collaborations.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology-Hartford CT/RI]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48655]]></requisitionid>
    <referencenumber><![CDATA[R48655]]></referencenumber>
    <apijobid><![CDATA[r48655]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48655/medical-specialist-i-pulmonology-hartford-ctri/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hartford]]></city>
    <state><![CDATA[Connecticut]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p>Location: <strong>Hartford, CT/RI - representative must reside within or close to the territory.</strong></p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Great Lakes)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48127]]></requisitionid>
    <referencenumber><![CDATA[R48127]]></referencenumber>
    <apijobid><![CDATA[r48127]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48127/field-reimbursement-manager-neurology-great-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Chicago (Metro) IL</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47243]]></requisitionid>
    <referencenumber><![CDATA[R47243]]></referencenumber>
    <apijobid><![CDATA[r47243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47243/senior-manager-field-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Field Medical Affairs – Oncology, Japan to join our Medical Affairs team, supporting our oncology portfolio in a field-based role. In this role, you will engage in scientific exchange and collaborate with therapeutic area experts to provide disease and product information, as well as support research initiatives. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Field-based.</p><br><p><strong>Discover your role:</strong></p><ul><li>Identify and maintain relationships with medical and therapeutic area experts, investigator targets, and develop associated action plans.</li><li>Respond to requests for information on study indications, disease states, and therapeutic areas, presenting scientific and clinical data to diverse audiences in a compliant manner.</li><li>Educate practitioners, payers, and researchers on disease management and therapeutic areas.</li><li>Attend medical conferences to gather and share scientific, clinical, and competitive intelligence with internal stakeholders.</li><li>Support the investigator-initiated study program by building scientific relationships with investigators and identifying research opportunities.</li><li>Collaborate with Clinical Development, Clinical Operation, and trial staff to support site initiation, enrollment, and execution of Medical Affairs strategies.</li><li>Develop and implement rules and procedures for Field Medical activities to ensure compliance with relevant laws, regulations, guidelines, policies, and industry standards.</li><li>You excel in working collaboratively within a matrix organization and cultivating relationships in academic and clinical practice settings.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>A healthcare or scientific professional (PhD, MD, PharmD) with oncology experience and/or clinical trial experience. A Master’s Degree with extensive oncology expertise may be considered.</li><li>Deep knowledge and significant experience in lung cancer/solid tumors or hematology oncology; immuno-oncology experience is preferred.</li><li>At least 3 years of relevant experience in the pharmaceutical industry or clinical settings such as drug information, disease management programs, or clinical pharmacy/medicine.</li><li>Strong communication skills and fluency in Japanese and English.</li><li>Ability to travel 30–50%.</li><li>Experience working in a matrix organization and collaborating with academic and clinical practice settings.</li><li>A commitment to adhering to compliance culture and standards.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Associate Process Scientist]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48793]]></requisitionid>
    <referencenumber><![CDATA[R48793]]></referencenumber>
    <apijobid><![CDATA[r48793]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48793/temp-associate-process-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temporary Associate Process Scientist </strong>to join our <strong>Process Sciences Lab </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick.</li><li>This is a 12-month contract position.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Supporting the delivery of process solutions to IOPS and contributing to best-in-class laboratory and process validation report packages.</li><li>Assisting in the root cause analysis of process related deviations using scientific data–driven rationale.</li><li>Participating in cross functional teams to understand process issues in technical and laboratory investigations.</li><li>Contributing to the knowledge-based reports summarising conclusion of studies, investigations and process improvements.</li><li>Presenting findings at group meetings.</li><li>Producing and maintaining accurate records in accordance with site procedures and guidelines.</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Ability to work well in a team environment.</li><li>You can demonstrate strong communication and interpersonal skills.</li><li>You possess logical troubleshooting and problem-solving skills.</li><li>You have strong written and report writing skills.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Assoc Process Scientist: BSc/MSc Biotechnology, Biochemistry, or related field will be considered or equivalent combination education and experience.</li><li>Process Scientist: BSc Biotechnology, Biochemistry, or related field with 2 years’ experience; MSc Biotechnology, Biochemistry, or related field with 1 year experience.</li></ul><h3>Thrive today. Grow tomorrow.</h3><h3>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLPS</h3><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Change Control Specialist]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49439]]></requisitionid>
    <referencenumber><![CDATA[R49439]]></referencenumber>
    <apijobid><![CDATA[r49439]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49439/change-control-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill multiple Change Control Specialist positions. These positions develop strategic plans related to change control and the implementation of robust corrective actions to support manufacturing operations by applying function expertise.</p><p><strong>Current Departments with Openings:</strong></p><ul><li><p>Bulk Drug Substance Manufacturing</p></li><li><p>Technical Operations</p></li><li><p>Fill/Finish Manufacturing</p></li></ul><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Craft business plans to independently advance change control initiatives to implement Corrective and Preventative Actions (CAPA’s) and process improvements in support of manufacturing operations</p></li><li><p>Assess sophisticated proposed change controls to evaluate if proposal satisfies company standards</p></li><li><p>Coordinate and prepare change control documentation that assesses and defines the scope, impact, risk, and regulatory impact associated with the change</p></li><li><p>Review, edit, and revise controlled documentation in accordance with cGMP standards</p></li><li><p>Coordinate and/or lead cross-functional meetings with multiple departments to drive change control implementation</p></li><li><p>Provide advice and mentorship to cross-functional teams to enable successful and GMP compliant change controls</p></li><li><p>Independently monitor and progress multiple projects concurrently – identifying, addressing, and/or raising potential obstacles in a timely manner</p></li><li><p>Present business critical and regulatory impactful change controls to senior leadership</p></li><li><p>Document all training</p></li><li><p>Assist with the training of new employees</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in Life Sciences, Engineering, or related field; or equivalent combination of education and experience, and the following amount of experience for each level:</p><ul><li><p>Associate Change Control Specialist: 0-2+ years of relevant experience</p></li><li><p>Change Control Specialist: 2+ years of relevant experience</p></li><li><p>Senior Change Control Specialist: 5+ years of relevant experience</p></li><li><p>Level will be determined based on experience</p></li></ul></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Quality Assurance, Drug Substance Manufacturing]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48628]]></requisitionid>
    <referencenumber><![CDATA[R48628]]></referencenumber>
    <apijobid><![CDATA[r48628]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48628/director-quality-assurance-drug-substance-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Saratoga Springs]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of Quality Assurance to provide quality leadership for the startup and long-term operations of the Regeneron Drug Substance manufacturing facility located in Saratoga Springs NY, a greenfield biologics site scheduled to begin operations in 2028. The position is responsible for building the QA organization and digital processes needed to support facility design, commissioning, qualification, and startup, and for the ongoing QA oversight of a fully automated “plant of the future” built around high levels of technology integration, data integrity, and review-by-exception batch disposition. The director will define the quality process, automation and data requirements needed to enable review by exception and will provide leadership and direction across cell culture, centrifugation, chromatography, UFDF, and aseptic dispensing operations, ensuring compliance with current FDA and International Regulatory Body requirements.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Saratoga Springs, NY and Rensselaer, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead the QA startup strategy for the Saratoga Drug Substance facility, including quality systems build-out, staffing, and readiness for design review, commissioning, qualification, and process validation</p></li><li><p>Define the automation, systems integration, and data integrity requirements (e.g., MES, DCS/SCADA, historian, LIMS) needed to enable review-by-exception batch record disposition</p></li><li><p>Partner with Automation, Engineering, and IT/Data Integrity functions to design exception-based quality control strategies, including electronic batch record rules, automated in-process checks, and real-time release criteria</p></li><li><p>Build and execute a business strategy that translates vision and corporate goals into departmental objectives for a highly automated plant of the future</p></li><li><p>Builds and maintains a high performing team of managers, providing effective alignment and communication with functional groups at the site and at other manufacturing sites, to successfully deliver on all commitments. Sets the course for the future- defines priorities, goals and objectives for quality team</p></li><li><p>Provide direction, set performance standards, evaluate, develop performance and inspire direct reports</p></li><li><p>Drives departments for optimal performance and constantly raises the bar, accountable for the performance and results of a department</p></li><li><p>Ensure manufacturing quality staff are appropriately trained to support a highly automated, review-by-exception environment. Responsibilities include exception review, in-process testing oversight, batch record review, and quality-on-the-shop-floor responsibilities of first response to product quality issues in production</p></li><li><p>Provide career development and training advice. Provide regular feedback to direct reports on company and departmental operations</p></li><li><p>Establishes data integrity governance for automated systems, ensuring ALCOA+ principles and 21 CFR Part 11/Annex 11 compliance are designed into the facility from startup</p></li><li><p>Directs the activities of resources, both internal and outside contractors/vendors/systems integrators, with similar technical or functional responsibilities supporting facility digital startup and automation design</p></li><li><p>Lead cross functional teams and manages the deliverables for the assigned projects. Drives projects through completion within timeline, quality and budgetary constraints. Interfaces with senior management to report on project and program milestones and to present project needs</p></li><li><p>Accountable for ensuring policies, procedures, and standards are established, consistently followed, and adhered to on a consistent basis; develops new quality systems appropriate for a fully automated facility</p></li><li><p>Provides first response for Quality and Compliance issues on the manufacturing floor.</p></li><li><p>Provides review and final QA approval of deviations, and other quality events; protocols/reports; change documentation, SOPs; master batch record approval, including automation/system-based release logic</p></li><li><p>Ensures product, facility, and equipment holds are placed when batch, equipment or system integrity is questioned</p></li><li><p>Responsible for representing the Company and directly interfacing with auditors during regulatory body inspections, including inspections of automation and data integrity systems</p></li><li><p>Ensures periodic informal audits are completed in production</p></li><li><p>Leads teams for tracking of quality activities, metrics, CAPA tracking, etc. Reports metrics and assesses data trends to work with operating departments to facilitate process improvements</p></li><li><p>Responsible for implementing and improving operational and strategic policies and directives</p></li><li><p>Develops or supports program development for cell culture operations, centrifugation/harvest, chromatography, UFDF, viral clearance, and aseptic dispensing in an automated environment</p></li><li><p>Provide leadership and direction to ensure a constant state of inspection readiness for a newly commissioned facility</p></li><li><p>Requires the ability to influence others to achieve results and to challenge the status quo in designing and operating a plant of the future</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in Life Sciences, Engineering, or related field with at least 12+ years experience in a Quality Operations, Quality Management or manufacturing role, in cGMP biologics/Drug Substance manufacturing</p></li><li><p>4 + years experience in a leadership role</p></li><li><p>Experience with facility startup, commissioning, qualification, and process validation for greenfield or new manufacturing facilities is required</p></li><li><p>Experience with automation systems (MES, DCS/SCADA), data integrity requirements, and review-by-exception quality models is highly preferred</p></li><li><p>Experience with cell culture, centrifugation, chromatography, UFDF, and aseptic dispensing operations is beneficial</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quality Assurance Validation Specialist]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49489]]></requisitionid>
    <referencenumber><![CDATA[R49489]]></referencenumber>
    <apijobid><![CDATA[r49489]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49489/senior-quality-assurance-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Senior QA Validation Specialist, you will validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li></ul><p><strong>What you’ll do: </strong></p><ul><li>Generates, executes and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria</li><li>Analyzes the results of testing and determines the acceptability of results against pre-determined criteria</li><li>Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements</li><li>Reviews, edits and approves deviation notifications, deviation investigations, and corrective actions</li><li>Reviews, edits and approves change controls, SOPs, reports and other documentation</li><li>Coordinates with other departments or outside contractors/vendors to complete validation tasks Executed real-world and simulated transport studies, including gross-damage visual inspections, pallet configuration assessments, and qualification of secondary and tertiary packaging materials</li><li>Conducts temperature mapping for controlled environments and distribution lanes</li><li>Programs and deploys instrumentation to capture vibration and shock profiles; analyzed data to inform packaging design and handling recommendations</li><li>Programs humidity and pressure sensors and interpreted datasets to support test plans and root-cause analysis</li><li>Applies ASTM and/or ISTA standards to cold-chain shipping design, testing, and qualification</li><li>Performs small-parcel and palletized-load qualifications, including test planning, execution, and reporting</li></ul><p><strong>Gowning and Environment: </strong></p><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>QA Validation Specialist: 4 + years of experience</li><li>Sr. QA Validation Specialist: 6+ years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Apprentice I - Electrical Instrumentation]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49434]]></requisitionid>
    <referencenumber><![CDATA[R49434]]></referencenumber>
    <apijobid><![CDATA[r49434]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49434/apprentice-i-electrical-instrumentation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Apprenticeship programme is crafted to provide apprentices with the required knowledge, skills, and competence to perform as a qualified craftsperson. Under the mentorship of expert technicians, the Apprentice is primarily responsible for providing a support service to the site as part of the Technical Operations team specializing in Electrical and Calibration activities.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Completing all training, both on and off site phases as per SOLAS Electrical Instrumentation Apprenticeship training programme curriculum</p></li><li><p>Providing Electrical/ Instrumentation/Calibration support to the Technical Operations, Quality Assurance, Engineering and Operations teams or any other area as the need arises</p></li><li><p>Being responsible for installing, testing and solving site electrical systems, PLC’s (Programmable Logic Controllers), PAT (Portable Appliance Testing) and carrying out assigned electrical duties</p></li><li><p>Completing both scheduled and unscheduled Electrical and Calibration maintenance activities</p></li><li><p>Working on automated control systems and with low voltage systems</p></li><li><p>Loop checking, tuning, troubleshooting and start-up of instrumentation</p></li><li><p>Calibrating of various types of instrumentation including temperature, pressure, level, flow and analytical instruments or others as the need arises</p></li><li><p>Aligning with site Environmental, Health and Safety policies and striving to maintain an accident free environment</p></li><li><p>Ensuring documentation of maintenance activities to current GxP standards both in paper based records and the computerized maintenance system</p></li><li><p>Maintaining the physical condition and environment of all areas</p></li><li><p>Following current good manufacturing practices (cGMPs)</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have a strong technical capability</p></li><li><p>You enjoy hands on learning</p></li><li><p>You want to work in an environment that promotes continuous learning and development</p></li><li><p>You want real world experience across all areas of a large Biopharmaceutical worksite</p></li><li><p>You enjoy working as part of a successful team</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><p>To be considered for this opportunity you should have a Leaving Certificate qualification to include a math’s and a science or engineering subject.</p><p><strong>Hourly Rate Year 1 </strong></p><p>€ 14.15</p><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€0.00 - €0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Assistant General Counsel – Market Access Legal]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48766]]></requisitionid>
    <referencenumber><![CDATA[R48766]]></referencenumber>
    <apijobid><![CDATA[r48766]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48766/senior-director-assistant-general-counsel-market-access-legal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build Our Future Together</strong></p></div><p>The Senior Director, Assistant General Counsel – Market Access Legal will provide proactive, efficient, strategic, and collaborative legal support to Regeneron’s Market Access Commercial Business Unit. More specifically, this person will advise a wide range of internal Market Access and other clients, including Market Access Strategy; National and Regional Payer Account Teams; the Government Pricing, Contract Strategy, Pricing, and Operation Team; as well as Commercial; Marketing; Sales; Public Policy and Government Affairs; Regulatory; and Corporate Compliance. The level of counseling requires a deep understanding of market access principles, market access strategy, payers, pharmacy benefit managers (“PBM”), payer and PBM contracts, pharmaceutical distribution channels, contract operations, government pricing, regulatory and compliance issues, the False Claims Act, the Anti-Kickback Statute, and OIG guidance, and other applicable state and federal healthcare laws. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Work model/flexibility: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing proactive, efficient, strategic, and collaborative legal advice and support on market access, market access strategy, payer and PBM contracts, payer and PBM strategies, government pricing, and other Commercial-related matters in a fast-paced environment</p></li><li><p>Providing legal guidance on various issues, tactics, and activities, including market access strategy development, creation of market access materials, contract drafting and negotiation, government pricing reporting, and interactions with healthcare providers, distributors, pharmacies, payers, PBMs, and GPOs</p></li><li><p>Drafting and negotiating a wide variety of commercial contracts including payer and PBM agreements, GPO agreements, distribution agreements, pharmacy agreements, rebate agreements, service agreements, and other corporate agreements</p></li><li><p>Provide support to various Commercial teams and Product Attorneys on product-specific Market Access issues</p></li><li><p>Provide support to Corporate Compliance on Market Access issues</p></li><li><p>Maintain an independent and objective perspective while developing and maintaining a strong partnership with the client organizations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Juris Doctor degree with 10+ years relevant legal experience</p></li><li><p>Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel</p></li><li><p>Prior in-house healthcare/pharmaceutical and/or biotech experience required</p></li><li><p>Significant knowledge of life sciences regulatory enforcement trends, market access, market access strategy, payer and PBM-related issues, payer and PBM contracts, other market access contracts, contract operations, government pricing requirements (ideally for both medical and pharmacy benefit products), regulatory and compliance issues, the FDCA, the False Claims Act, federal and state fraud and abuse laws, and antitrust laws</p></li><li><p>Excellent interpersonal and conflict resolution skills, and ability to work in highly collaborative, team-oriented environment</p></li><li><p>Excellent understanding of healthcare laws and proven experience in applying them to complex business situations</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49652]]></requisitionid>
    <referencenumber><![CDATA[R49652]]></referencenumber>
    <apijobid><![CDATA[r49652]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49652/principal-business-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is looking for an outstanding Principal Business Analyst to drive consistency across the Global Development (GD) IT team, and be a member of the GD Digital Transformation Program. This individual will work closely with GD IT leadership, and GD partners such as Business Process Owners, Subject Matter Experts, Training and Process & Procedures teams members in support of the overall Program and specific use cases.</p><p><strong>Where: </strong>Based at our Warren, NJ location</p><p><strong>When: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Collaborate with GD IT Leadership to support the GD Digital Transformation Program, including overall program management.</p></li><li><p>Support the delivery of a GD Digital Transformation Program “use case” (new digital solution to improved efficiency and ways of working across GD)</p></li><li><p>Develop frameworks to gather accurate, measurable requirements that dictate project outcomes</p></li><li><p>Build flexible processes and frameworks in support of traditional (e.g., waterfall) and hybrid (e.g., agile) delivery methods</p></li><li><p>Collect GD IT operational metrics, analyze, identify & develop action plans for areas of improvement</p></li><li><p>Introducing new insights, approaches, solutions and technologies for GD IT</p></li><li><p>Collaborating with GD IT agile Delivery & Operations and Data Enablement leads to ensure that solutions are appropriately planned, accomplished, and improved upon</p></li><li><p>Provide direction on projects and technology products to optimally manage user expectations, timelines, budget and overall efforts for value realization</p></li><li><p>Work collaboratively with GD functions, Corporate IT, and other relevant functions in the management of enterprise systems, including development and adherence to standards and governance</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Bachelor's degree in a related field BS/BA Degree </p></li><li><p>7+ years of relevant work experience</p></li><li><p>Knowledge of pharmaceutical Global Development business capabilities, processes, applications, and key trends in the industry</p></li><li><p>Experience in one or more of the following Clinical Development functions in support of IT: Medical Affairs, Regulatory Affairs, Global Patient Safety, Clinical Operations, Biostatistics & Data Management, Clinical Quality, etc.</p></li><li><p>Robust business acumen and analytical expertise, to consistently drive operational enhancements and work practices' optimization</p></li><li><p>Self-drive & ability to work in ambiguity, with minimal oversight</p></li><li><p>Basic to intermediate proficiency in AI tools (e.g. CoPilot), and building AI agents</p></li><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders</p></li><li><p>Experience with Waterfall/Hybrid/Agile project methodologies and associated tools (e.g., Jira, Confluence)</p></li><li><p>Strong track record of technology project, stakeholder, and budget management</p></li><li><p>Ability to coordinate, influence and empower diverse teams to achieve goals</p></li><li><p>Experience working within and knowledge of GXP/GCP and regulatory ICH 6 guidelines</p></li><li><p>Expertise with MS Office Suite</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Precision Medicine]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44954]]></requisitionid>
    <referencenumber><![CDATA[R44954]]></referencenumber>
    <apijobid><![CDATA[r44954]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44954/director-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Precision Medicine Strategy Lead (Director level) to join our Precision Medicine group, independently overseeing the development and execution of biomarker strategies across one or more therapeutic areas, with a preference for obesity/metabolism, as well as Neurodegenerative Disorders, Cardiovascular Disease, Muscle and Metabolism Disorders, and/or Rare Genetic Diseases. In this highly matrixed role, you will design, develop, communicate, and operationally implement clinical biomarker strategies, collaborating with discovery research, clinical operations, internal laboratories, and allied company partners to support key programs in early and late-stage drug development.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Lead the strategic vision for clinical biomarkers in one or more therapeutic areas, enabling advances in target identification, indication selection, and patient stratification</p></li><li><p>Serve as a senior-level Precision Medicine representative on development teams, delivering biomarker strategies from concept to execution and results interpretation</p></li><li><p>Collaborate with Discovery Research and product development teams to incorporate biomarker strategies for molecules in discovery phases</p></li><li><p>Represent Regeneron with allied companies to develop and implement biomarker strategies for partnered alliances</p></li><li><p>Partner with clinical operations teams to implement biomarker and exploratory sample collection and analyses across studies</p></li><li><p>Design, oversee, and manage internal and external research collaborations in clinical technologies and translational research</p></li><li><p>Ensure complex clinical assays are fit-for-purpose, whether developed and validated internally or externally</p></li><li><p>Contribute to and ensure the quality of technical reports, study memos, clinical study reports, and scientific publications</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D. and 10+ years of experience driving, managing, executing, and delivering results for complex, multi-functional projects</p></li><li><p>Excellent communication and presentation skills, with high emotional intelligence</p></li><li><p>Strong organizational and team collaboration skills</p></li><li><p>Strong track record in mentorship and development of direct reports</p></li><li><p>Deep experience in biomarker assay development and validation in clinical drug development, with a focus in therapeutic areas outside of Oncology</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY- WASHINGTON, DC]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48926]]></requisitionid>
    <referencenumber><![CDATA[R48926]]></referencenumber>
    <apijobid><![CDATA[r48926]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48926/medical-account-specialist-ii-hematology-washington-dc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Washington, DC</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) -Oncology *Okayama Area]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49190]]></requisitionid>
    <referencenumber><![CDATA[R49190]]></referencenumber>
    <apijobid><![CDATA[r49190]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49190/medical-representative-mr-oncology-starokayama-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist, Oncology to join our Oncology Sales team, supporting our oncology business area in a field-based role. In this role, you will drive the adoption of our oncology product portfolio while collaborating with healthcare professionals and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><br></p><p><strong>When & where:</strong></p><p>You will be responsible for the Okayama area.</p><p>Your residence is expected to be in Okayama.</p><p><br></p><p><strong>Discover your role:</strong></p><ul><li>Drive sales and adoption of the oncology product portfolio within assigned territory</li><li>Develop and execute territory business plans to achieve sales targets</li><li>Build and maintain relationships with healthcare professionals and key accounts</li><li>Deliver approved scientific and clinical information to support customer decisions</li><li>Identify and engage new business opportunities in the oncology space</li><li>Collaborate with cross-functional teams to support customer needs</li><li>You adapt to evolving priorities and thrive in a results-driven environment</li><li>You demonstrate strong communication and relationship-building skills</li></ul><p><br></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in life sciences, business, or related field</li><li>Proven sales experience in the pharmaceutical, biotech, or healthcare industry</li><li>Knowledge of oncology or related therapeutic area</li><li>Strong communication, presentation, and negotiation skills</li><li>Ability to travel within assigned territory as required</li><li>Driver license and MR certification</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Operational Technology (OT) Data]]></title>
    <date><![CDATA[Fri, 17 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46099]]></requisitionid>
    <referencenumber><![CDATA[R46099]]></referencenumber>
    <apijobid><![CDATA[r46099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46099/process-development-engineer-iii-operational-technology-ot-data/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer III, OT Data Systems</strong> to join our Data Enablement and Analytics (DEA) team within the Product, Analytics and Process Development (PAPD) organization. In this role, you will drive the design, evolution, and governance of Operational Technology (OT) data systems that deliver high-quality data to lab specialists for real-time decision-making and offline analysis, while collaborating with lab specialists, IT teams, and distributed data managers across the organization. You'll implement value-focused data management solutions that increase asset value, meet immediate business needs, and build scalable data capabilities for the future.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: On-Site</li><li>Shift Requirements: Full-time, standard business hours, with flexibility to support before- and after-hours</li></ul><h3>Discover your role:</h3><ul><li>Provide technical leadership for OT data platforms, defining architecture principles and best practices that improve reliability and usability</li><li>Establish standards, controls, and audits to ensure OT data availability, integrity, quality, security, and accessibility</li><li>Coach and mentor distributed data managers and junior engineers, setting technical direction and reviewing designs</li><li>Partner with lab specialists and IT to integrate process control and data acquisition systems into a unified architecture</li><li>Lead IT/OT convergence initiatives, aligning cybersecurity posture, compliance, and network segmentation</li><li>Translate user requests into prioritized backlog items and run grooming and planning sessions</li><li>Drive incident triage and root-cause remediation while proactively monitoring system health</li><li>Serve as OT subject matter expert, leading evaluations of new platforms and presenting recommendations</li></ul><h3><strong>This role might be for you if:</strong></h3><ul><li>You champion data-driven decision making and can articulate trade-offs across performance, security, compliance, and cost</li><li>You uphold high standards for accuracy, quality, and attention to detail</li><li>You balance near-term delivery with long-term platform health, managing technical debt deliberately</li><li>You enjoy mentoring, growing talent, and building repeatable processes that elevate team outcomes</li><li>You thrive communicating with technical and non-technical partners across cross-functional environments</li><li>You're comfortable translating complex requirements into secure, scalable, maintainable solutions</li></ul><h3>This role requires:</h3><ul><li>BS in Computer Science, Information Systems, Biomedical/Chemical/Electrical Engineering, or related field with 10+ years of experience, or MS with 7+ years, or PhD with 0-3 years</li><li>5+ years of experience with AVEVA PI System (Data Archive, Asset Framework) and Ignition SCADA, including high-availability design and data modeling</li><li>SQL experience in a database owner role</li><li>Demonstrated proficiency in design, deployment, and lifecycle management of OT data systems across high-availability industrial architectures</li></ul><h3><strong>Preferred / Nice to haves:</strong></h3><ul><li>Familiarity with control systems architecture and industry standards/protocols (ISA-95, S88, OPC, MQTT)</li><li>Working knowledge of continuous and batch manufacturing processes and related data/analytics tools</li><li>Foundational knowledge of lab-based automation software (e.g., Unicorn, Biobrain Supervise, FactoryTalk, Empower)</li><li>Growing proficiency in Python for automation, data pipelines, and tooling</li><li>Familiarity with Industry 4.0, digitalization, and IT/OT convergence concepts</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[GMP Data Governance Lead]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49819]]></requisitionid>
    <referencenumber><![CDATA[R49819]]></referencenumber>
    <apijobid><![CDATA[r49819]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49819/gmp-data-governance-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a GMP Data Governance Lead at the Principal or Staff level to join our Quality Assurance team. In this role, you will be responsible for fostering a culture of data governance within the site by ensuring compliance with Data Governance policies; designing and delivering relevant training; and monitoring Data Governance practices. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When and where?</strong></p><ul><li><p>Location: Troy, NY</p></li><li><p>Work schedule: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong> </p><ul><li><p>Leading and managing the team of Engagement, Culture & Monitoring (ECM) specialists</p></li><li><p>Driving successful stakeholder engagement and management across the sites</p></li><li><p>Promoting a mature Data Governance culture through working in conjunction with the Global DG (Policy & Programs) Team to design & deliver continuous DG Training in line with current and evolving required DG knowledge, skills, and awareness needs</p></li><li><p>Designing and developing comprehensive training programs focused on DG, compliance with regulations, and best practices for bio-pharmaceutical manufacturing</p></li><li><p>Conducting and facilitating Data Governance focused training sessions, workshops, and seminars for staff at various levels within the organization</p></li><li><p>Leveraging technology to improve training delivery, including e-learning platforms, simulation tools, and virtual training environments</p></li><li><p>Building awareness through engagement with employees of the need for and the desire to build & role model a mature Data Governance culture</p></li><li><p>Acting as Data Governance advocates with Data Stewards on the culture & behavioral changes required, why, and steps that can be taken to develop an open & transparent DG culture.</p></li><li><p>Gathering agreed site Data Governance KPIs and reporting their findings to the DG Business Partners</p></li><li><p>Establishing ongoing monitoring and auditing processes to ensure Data Governance cultural improvements are sustained</p></li><li><p>Collaborating with other ECM Experts, Technical DG Experts & Business Partners to deliver on the plan and feedback themes to allow Continuous Improvement & evolution of the Data Governance approach</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BA/BS degree and the following amount of experience in pharmaceutical/FDA regulated work areas such as: data management & operations, quality assurance, compliance, manufacturing operations, quality control, or IT, or equivalent combination of education and experience, for each level:</p><ul><li><p>Principal Specialist: 8+ years</p></li><li><p>Staff Specialist: 10+ years</p></li><li><p>Level will be determined based on experience</p></li></ul></li><li><p>Demonstrated success in designing, implementing, and managing training programs for diverse audiences</p></li><li><p>Experience with training management systems and e-learning tools (e.g., LMS, Articulate)</p></li><li><p>Strong analytical skills and attention to detail</p></li><li><p>The ability to collaborate with other ECM Experts, Data Governance Business Partners, Technical Experts and cross-functional teams</p></li><li><p>Ability to translate complex regulatory and technical requirements into clear guidance for cross-functional teams</p></li><li><p>Strong stakeholder management and influencing skills</p></li><li><p>Experience in cultural/people change management and organizational development</p></li><li><p>Knowledge of applicable federal, state, and local regulations (e.g. GDPR), rules, policies, and procedures such as FDA Guidance on Data Integrity, EMA Data Integrity Guide, and WHO Guide to Data Integrity</p></li><li><p>Knowledge of cGMP & GDP</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Assay Development]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46564]]></requisitionid>
    <referencenumber><![CDATA[R46564]]></referencenumber>
    <apijobid><![CDATA[r46564]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46564/senior-associate-scientist-assay-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Associate Scientist Bioanalytical Assay Development USA to join our Assay Development Group, supporting our Bioanalytical Sciences organization in a hybrid work mode. In this role, you will support preclinical and clinical assay development activities while collaborating with cross-functional scientific teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Tarrytown, NY</p><p>On-site</p><p><strong>Discover your role:</strong></p><ul><li>Plan, initiate, and execute qPCR, digital droplet PCR (ddPCR), and ELISA assays.</li><li>Prepare samples and perform assay runs supporting preclinical and clinical programs.</li><li>Process assay data and maintain compliance with current GxP documentation practices.</li><li>Document findings and laboratory records within an electronic laboratory notebook.</li><li>Evaluate new technologies and assay formats to advance development capabilities.</li><li>Maintain Good Laboratory Practice (GLP) compliance for validations under FDA regulations and SOPs.</li><li>Present scientific data in formal and informal meetings.</li><li>You thrive in a collaborative environment and take ownership of deliverables.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in biology or a related field; Master's degree preferred.</li><li>3 to 6+ years of relevant laboratory experience.</li><li>Hands-on experience with quantitative PCR (qPCR) and digital droplet PCR (ddPCR).</li><li>Understanding of methodologies used to assess DNA and RNA.</li><li>Experience performing biochemical, molecular, and immune-based assays, including ELISA.</li><li>Ability to manage multiple assays and projects simultaneously.</li><li>Experience maintaining GxP documentation and GLP-compliant laboratory records.</li><li>Experience with electronic laboratory notebooks.</li><li>Prior experience in gene therapy and/or bioanalytical assay platform development is highly desirable.</li><li>Strong problem-solving, prioritization, communication, and organizational skills with the ability to work independently.</li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  ORLANDO, FL]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48921]]></requisitionid>
    <referencenumber><![CDATA[R48921]]></referencenumber>
    <apijobid><![CDATA[r48921]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48921/medical-account-specialist-ii-hematology-orlando-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Orlando, FL</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47175]]></requisitionid>
    <referencenumber><![CDATA[R47175]]></referencenumber>
    <apijobid><![CDATA[r47175]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47175/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Project Engineer to join our growing Project Engineering team. In this role, you will design, specify, and commission new and renovated process and clean utility equipment. You will lead deviation investigations and provide engineering support across manufacturing processes. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Troy, NY</li><li>Work model: Monday-Friday 8:00am-4:30pm</li><li>Travel: up to 10%, domestic and international</li></ul><br><h3>Discover your role:</h3><ul><li>Design and specify cGMP process equipment, piping, and controls, including engineering documentation.</li><li>Manage mid-to-large projects for process equipment and clean utilities, including start-up, commissioning, and site acceptance.</li><li>Lead design review and installation of equipment.</li><li>Prepare piping and instrumentation diagrams and develop Process Flow Diagrams.</li><li>Support QA/Validation with design documents and protocol execution.</li><li>Investigate process equipment, utility, and control system anomalies, implementing corrective and preventive actions.</li><li>Supervise mechanical, electrical, and automation contractors.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree in Chemical Engineering, Biochemical Engineering, or another relevant Engineering discipline.</li><li>5+ years of project/process engineering experience for Senior Project Engineer, or 8+ years for Principal Project Engineer.</li><li>Direct experience with biopharmaceutical process equipment is preferred.</li><li>Solid understanding of process control systems and automation.</li><li>Thorough knowledge of engineering documentation for cGMP process equipment and sanitary equipment design requirements.</li><li>Experience planning and tracking project activities and schedules.</li><li>Strong interpersonal and cross-cultural communication skills, with the ability to lead without direct authority.</li><li><strong>Gowning and Physical Requirements:</strong></li><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, IT Laboratory Informatics]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45565]]></requisitionid>
    <referencenumber><![CDATA[R45565]]></referencenumber>
    <apijobid><![CDATA[r45565]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45565/senior-manager-it-laboratory-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Manager (Manager or Senior Manager) to join our IOPS IT team, overseeing the day-to-day maintenance, support, and development of Regeneron's IT Applications portfolio — including Empower CDS, SDMS, and other business-critical systems. In this role, you will lead a team of analysts, drive audit readiness and compliance, and ensure applications are maintained in a validated and compliant state — while collaborating closely with peer managers, QA, IT leadership, and global counterparts. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead and develop a team of IT Applications analysts through performance management, coaching, mentoring, and goal setting; conduct monthly performance reviews and annual evaluations</li><li>Drive audit readiness across the application portfolio; serve as a key point of contact during FDA inspections and internal audits, ensuring systems, audit trails, and documentation are inspection-ready at all times</li><li>Ensure all supported applications are maintained in a compliant and validated state; proactively identify and resolve data integrity and compliance issues in accordance with 21 CFR Part 11, ALCOA+ principles, applicable SOPs, and policies</li><li>Maintain accuracy of system documentation including User Requirement Specifications, Design Specifications, Configuration Specifications, and Test Plans for validated systems</li><li>Collaborate closely with peer managers overseeing complementary application portfolios to ensure alignment, shared best practices, and coordinated delivery across the broader IOPS IT Applications function</li><li>Partner with global counterparts to support and maintain globally deployed QC systems in a consistent and compliant manner</li><li>Manage vendor relationships including performance, contract adherence, and delivery of services in line with business and regulatory compliance requirements</li><li>Develop and implement operational metrics and controls; drive continuous improvement initiatives that enhance workflows, system reliability, and team efficiency; contribute to the strategic vision of the IOPS IT Applications function</li><li>Strong knowledge of cGMP, GAMP, 21 CFR Part 11, and Annex 11; experience supporting applications in a highly regulated GMP laboratory or IT environment preferred</li><li>Demonstrated understanding of ALCOA+ principles and data integrity requirements in biopharmaceutical production</li><li>Proven ability to lead teams through FDA inspections and internal audits with confidence and thoroughness</li><li>Knowledge of Regulatory Asset Manager systems advantageous</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Information Technology, Science, Engineering, Computer Science, or a related field</li><li>Manager: 7+ years of relevant experience with 3+ years managing teams</li><li>Senior Manager: 8+ years of relevant experience with 4+ years managing teams</li><li>May consider experience in lieu of education. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Consumer Marketing (Ophthalmology)]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46178]]></requisitionid>
    <referencenumber><![CDATA[R46178]]></referencenumber>
    <apijobid><![CDATA[r46178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46178/associate-director-consumer-marketing-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Marketing will contribute to the financial success of the Ophthalmology franchise. Main area of responsibility will be to implement and manage key elements of the U.S. Consumer Marketing plan, ultimately to drive demand for the product.</p><p>Specifically, this will include omnichannel campaign implementation including, Television, Print/Mail, digital and social media marketing execution, patient engagement tool/material development, patient education plan development and implementation, strategic content creation, Agency collaboration, materials and inventory management, budget management, management of review materials schedule and process.</p><h3>When & where:</h3><ul><li>Office Based in Sleepy Hollow, NY for 4 days a week with ~10% travel expected</li></ul><br><h3>Discover your role:</h3><ul><li><p>Contributing to, and implementing consumer strategy, communications planning and tactical plans</p></li><li><p>Implementation of consumer initiatives and tactical plans</p></li><li><p>Delivering against omnichannel strategy and optimizing performance media programs against business goals and priorities</p></li><li><p>Manage & provide strategic input to Agency-led media planning that delivers against the goals of the business</p><ul><li><p>Evaluate, and provide feedback to, performance of media buys in an ongoing way ensure alignment with brand objectives</p></li><li><p>Work with internal Insights & Analytics Teams to expand our approach to measurement of campaigns and other omnichannel initiatives</p></li></ul></li><li><p>Developing innovative digital and social media programs that accelerate brand awareness and drive consumer action</p></li><li><p>Extend omnichannel strategies through an understanding of technical, data, and media system integration points and underlying platforms in a way that delivers incremental value to our customers, patients, and prospects</p><ul><li><p>Expand on compliant first-party data strategy that enriches our customer experience and drives value for our brand</p></li><li><p>Continue to refine our view of our customer, personas, segmentation, and related – business-critical user journeys</p><ul><li><p>Mature our approach to customer journeys in a way that delivers data, insights, and an evolution of our marketing activities</p></li></ul></li><li><p>Develop SEO-inspired content planning that delivers on the needs of our customers in a way that ladders up to critical success factors for our brand</p><ul><li><p>Content development in various formats including: long form, short form, video, social channel specific (Reddit vs Facebook vs LinkedIn), and email</p></li></ul></li><li><p>Develop a seamless holistic digital experience that fulfills on tactical goals including key site actions, engagement, and customer registrations for CRM programs</p></li><li><p>Enrich existing CRM strategy to be more inclusive of additional user needs, journeys, and conversion stages</p></li></ul></li><li><p>Driving selection of patient ambassadors and developing patient testimonials and videos</p></li><li><p>Implementing targeted communication programs</p></li><li><p>Representing promotional tactics for medical, legal, and regulatory team reviews and ensuring final deliverables are accurate and compliant.</p></li><li><p>Working closely with the cross functional marketing team</p></li><li><p>Managing budgets and closely monitoring performance, ensuring cost effective delivery of all programs while tracking and monitoring KPIs</p></li><li><p>Developing and managing patient education and engagement tools and materials- and related promotion through personal and digital distribution channels</p></li></ul><h3>This role requires:</h3><ul><li>Bachelor's Degree, MBA a plus.</li><li>Demonstrated experience in marketing of biologics preferred.</li><li>You have 10+ years of progressive marketing experience including at least 5 years in the Consumer space in pharmaceutical marketing.</li><li>Demonstrated omnichannel digital marketing experience.</li><li>Demonstrated Consumer marketing competencies in the pharmaceutical/biotech areas. Prior U.S. launch experience a plus.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director- Ophthalmology-New York & New Jersey]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49824]]></requisitionid>
    <referencenumber><![CDATA[R49824]]></referencenumber>
    <apijobid><![CDATA[r49824]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49824/regional-director-ophthalmology-new-york-new-jersey/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Regional Director will report to one of the Sales Directors, Ophthalmology, and will be responsible for leading a regional sales team in achieving assigned goals/objectives and to ensure compliance with Regeneron's policies and programs that govern the field sales activities. The Regional Director will have Medical Specialists reporting to him/her.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: New York & New Jersey</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Responsible for meeting and/or exceeding assigned sales performance objectives and ensuring specific account actions plans are aligned to the strategic initiatives of the brand.</p></li><li><p>Lead regional sales force activities including hiring, training, coaching, performance evaluation and development, while ensuring compliance to corporate policies.</p></li><li><p>Communicate expectations for utilization of approved promotional resources.</p></li><li><p>Ensure each employee is trained on and effectively implementing customer education.</p></li><li><p>Communicate most current knowledge of the industry and competitor products to regional teams.</p></li><li><p>Ensure appropriate engagement in industry related meetings, conferences, etc.</p></li><li><p>Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p></li><li><p>Collaborate with internal stakeholders and cross-functional partners to develop the appropriate business strategies that support brand objectives.</p></li><li><p>Establish cross-functional partnerships and leverage resources across the region to influence customer behavior.</p></li><li><p>Oversee customer relationships and manage critical relationships with both current and potential customers.</p></li><li><p>Build and sustain relationships with therapeutic leaders within the region.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's Degree required.</p></li><li><p>Minimum 10 years’ experience from within a pharmaceutical/biopharmaceutical industry and a minimum of 5 years of regional and/or line sales management experience preferred.</p></li><li><p>Experience in Biologics and buy and bill products or strong relevant experience in the Retina field required.</p></li><li><p>Must be based in, or located in close proximity to the assigned Region (relocation will not be provided).</p></li><li><p>Ability to travel (60-65%). </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$212,500.00 - $287,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, HCP Marketing - Dermatology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49593]]></requisitionid>
    <referencenumber><![CDATA[R49593]]></referencenumber>
    <apijobid><![CDATA[r49593]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49593/director-hcp-marketing-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director of HCP Marketing will lead healthcare professional marketing strategy and execution for Dermatology indications in the U.S. This highly visible role requires a forward-looking leader with deep marketing expertise and the ability to navigate complex alliance partnerships. The Director will partner closely with cross-functional and alliance teams to advance product growth, contribute to the financial success of the brand, and strengthen its leadership position in dermatology. This position reports to the Senior Director, Dermatology Marketing.</p><h3>When & where:</h3><ul><li>In the office located in Sleepy Hollow, NY for 4 days a week</li></ul><h3>Discover your role:</h3><ul><li>Leading the HCP marketing strategy for atopic dermatitis, ensuring full integration with the broader brand strategy.</li><li>Acting as a key advocate for the Dermatology strategy, clearly articulating priorities and ensuring alignment across Regeneron, Sanofi, and other critical stakeholders.</li><li>Overseeing the development of HCP promotion strategies, messages, and tactical campaigns tailored to Dermatologists and Advanced Practice Providers.</li><li>Building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</li><li>Driving strong cross-functional and alliance collaboration, partnering with Sales, Medical Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, and HEOR to deliver cohesive, compliant, and impactful initiatives.</li><li>Ensuring all marketing programs comply with corporate policies, regulatory/ethical frameworks, and alliance standards.</li><li>Managing marketing budgets, timelines, and deliverables to meet scope and performance expectations.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; MBA strongly preferred.</li><li>12+ years of progressive experience in the pharmaceutical/biotech industry or related field.</li><li>8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas.</li><li>Dermatology and/or Immunology marketing and sales experience strongly preferred.</li><li>Demonstrated success in navigating complex alliance or co-promotion partnerships.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Material Sciences Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49816]]></requisitionid>
    <referencenumber><![CDATA[R49816]]></referencenumber>
    <apijobid><![CDATA[r49816]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49816/principal-material-sciences-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Material Sciences Engineer to join our Drug Product Process Sciences team. This is a technical services department that deals with a range of scientific, technical, technical, technical, engineering and mathematical needs from the laboratory to the manufacturing floor. In this partially lab-based role you will focus on material science and provide technical support to manufacturing, quality, combination products, formulations, and CMC Regulatory for manufacturing processes from technology transfer and/or design transfer to post-commercial lifecycle management activities.</p><br><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li><li>Travel percentage: 5% domestic & occasionally international</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Applies materials expertise across polymer science, physics, metallurgy, ceramics, and composites, connecting structure, processing, properties, and performance to drive design, development, and life-cycle management in biomedical or biopharmaceutical environments</li><li>Provides technical support, guidance, and risk assessment related to materials science across technology transfer, design transfer, process control strategy, process validation lifecycle, and post-commercialization activities</li><li>Analyzes data and information—from development through late-stage characterization and at-scale manufacturing history—using statistics, engineering principles, and other techniques to drive insights into process performance and control</li><li>Applies engineering principles to develop and execute process controls and validation strategies, including support for laboratory and at-scale studies for process characterization and validation</li><li>Liaises with cross-functional departments (Combination Products, Manufacturing, Quality Control, Formulation Development, Advanced Therapies, Quality Assurance, and CMC Regulatory) to support process lifecycle management</li><li>Authors protocols, reports, and technical documents with conclusions grounded in process and product knowledge, and ensures SOPs, policies, and validation plans align with industry/regulatory expectations (e.g., ICH guidelines)</li><li>Supports audits/inspections and contributes to CMC sections of regulatory submissions as needed</li></ul><br><p><strong>This role requires:</strong></p><ul><li>BS in Materials Science Engineering or related Engineering field and 8+ years of relevant experience</li><li>M.S. or Ph.D. preferred</li><li>A background in aseptic processing, drug substance development, drug product development, combination product development</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Portfolio Governance]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48028]]></requisitionid>
    <referencenumber><![CDATA[R48028]]></referencenumber>
    <apijobid><![CDATA[r48028]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48028/director-portfolio-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Portfolio Governance to join our Development organization, supporting portfolio-level decision-making in an onsite role. In this role, you will own and evolve our governance framework, ensuring decisions are made at the right level, with the right information, at the right time, while collaborating with senior leaders, governance chairs, and cross-functional stakeholders to drive decision quality and reduce cycle time.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Work model/flexibility: Onsite in Tarrytown, NY</li><li>Travel percentage: Up to 10%</li></ul><p><strong>Discover your role:</strong></p><ul><li>Own and continuously evolve the governance framework to enable scalable, high-quality decision-making across the portfolio</li><li>Establish decision quality standards, ensuring options, trade-offs, risks, and recommendations are clearly articulated</li><li>Facilitate governance forums to drive structured discussions and actionable outcomes</li><li>Define governance performance metrics and translate insights into a closed-loop improvement model</li><li>Synthesize governance outputs into portfolio-level insights, surfacing cross-program risks and systemic bottlenecks</li><li>Partner with senior leaders and governance chairs to align priorities and reinforce governance expectations</li><li>Drive cross-forum integration to streamline escalation pathways and improve decision flow</li><li>Coach and develop team members, building the skills and capabilities needed for portfolio delivery</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Think systemically about how decisions get made and enjoy designing frameworks that scale</li><li>Communicate with confidence and clarity in front of senior executives</li><li>Build trust and influence across matrixed, cross-functional environments</li><li>Translate data and feedback into clear, actionable insights</li><li>Lead and develop high-performing teams with a coaching mindset</li><li>Bring a continuous-improvement mentality to complex, fast-paced work</li><li>Navigate ambiguity comfortably while driving structure and discipline</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree with 12+ years of experience in biotechnology, pharmaceutical development, or consulting</li><li>Proven experience designing governance frameworks, operating models, or decision-making processes</li><li>Strong analytical skills with the ability to translate data into insights and action</li><li>Exceptional executive communication and facilitation skills</li><li>Demonstrated experience leading and developing high-performance teams</li></ul><p><strong>Nice to haves:</strong></p><ul><li>Experience with process improvement methodologies (Lean, Six Sigma)</li><li>Experience leveraging technology and digital solutions (dashboards, workflow tools, analytics platforms) to enable scalable processes</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Drug Supply & Logistics]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48813]]></requisitionid>
    <referencenumber><![CDATA[R48813]]></referencenumber>
    <apijobid><![CDATA[r48813]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48813/senior-manager-clinical-drug-supply-logistics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The <strong>Senior Manager, Clinical Drug Supply & Logistics</strong> is responsible for providing oversight of individual or multiple clinical programs, forecasting Investigational Product (IP) supply requirements for multiple clinical trials, and for managing the IP distribution process to one or more clinical trials. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron SOPs / WPDs. Contributes to ongoing process improvement initiatives. This role applies to internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, as well as staff from quality, clinical compliance, regulatory, formulations, and IOPS (CMC, external manufacturing, stability).</p><br><h3>When & where:</h3><ul><li>Location: Armonk, NY / Warren, NJ / Cambridge, MA</li><li>Work model/flexibility: in office 3-4 days per week</li></ul><h3>Discover your role:</h3><p>Supply Planning</p><ul><li><p>Serves as lead drug supply manager of a program and/or individual studies for the functional area in supply planning, including demand forecasting according to IOPS requirements.</p></li><li><p>Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical development plan.</p></li><li><p>Works with clinical drug supply management to determine resourcing needs.</p></li><li><p>Provides input to the development of IP-related study documents including protocols, study and pharmacy manuals.</p></li><li><p>Responsible for working within established timelines of investigational product manufacturing, labeling, release, distribution and return/destruction, and/or helping to establish these timelines. </p></li></ul><p>Inventory tracking</p><ul><li><p>Manages and oversees investigational product (IP) inventory strategy; advises supply management team of potential shortages and defines resupply activities based on usage trends and projections.</p></li></ul><p>Shipments</p><ul><li><p>Oversees IP shipment orders according to supply plans or as requested by Clinical Trial Management team, to ensure timely and compliant shipment and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity and/or manages any/all aspects of the process.</p></li></ul><p>IVRS</p><ul><li><p>Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS.</p></li><li><p>Works with cross-functional teams to develop specifications and support user testing of IRT systems provided by 3rd party vendors.</p></li><li><p>Leads effort for clinical supply management functionality.</p></li><li><p>Monitors and manages clinical supply activities through IRT from study start-up through study closure.</p></li></ul><p>Returns & Destruction</p><ul><li><p>Develops strategy and oversees drug return and destruction activities.</p></li></ul><p>Expiry Management</p><ul><li><p>Develops resupply strategies based on stability and shelf-life of clinical supplies.</p></li><li><p>Monitors IP expiry data and informs Clinical Supply team and Clinical Trial teams of pending IP expiry.</p></li></ul><p>Ancillary & Comparator Supplies</p><ul><li><p>Coordinates with other functional areas, including Regulatory, Medical Director, Forecasting & Planning, and IOPS to define ancillary and/or comparator supply strategy.</p></li><li><p>Develops plans for supplying clinical study sites with ancillary and/or comparator supplies, either through in-house initiated supply or working with supply vendors.</p></li></ul><p>Documentation</p><ul><li><p>Provides input to drug kit randomization specifications and reviews and approves master kit lists.</p></li><li><p>Designs, reviews, and approves IP-related study tools (for clinical study teams and investigative site use), as needed.</p></li><li><p>Supports inspection team in preparation for and during regulatory agency inspection. May represent Clinical Drug Supply & Logistics during regulatory agency inspections.</p></li></ul><p>Study Team Interaction</p><ul><li><p>Represents Clinical Drug Supply & Logistics on cross-functional study team (s) and/or sub-team(s).</p></li><li><p>Prepares or provides input into IP-related content for training materials and coordinates training on study procedures; In collaboration with the CTM for study, provides input into IP-related study specific working practices; Establishes study team contacts, roles, responsibilities, and objectives for IP-related services; Develops, manages, and maintains relationships with external partners; Effectively communicates with CROs, shipping and IVRS vendors, study sites and study team members to ensure ongoing successful execution; Acts as point of escalation for IP-related issues.</p></li></ul><p>Budget Management</p><ul><li><p>Provides input into budgets, SoWs, contracts and timelines for IP-related services.</p></li><li><p>Creates RFPs, reviews quotes, and awards third-party vendors for distribution services.</p></li><li><p>Responsible for distribution vendor budget management (invoice review/approval, change orders, reconciliation); reviews and approves/scrutinizes specified costs on vendor invoices against contract, as delegated.</p></li></ul><p>Vendor Management</p><ul><li><p>Leads management of IP service vendors (performance, quality, timelines, deliverables, costs)</p></li><li><p>Participates in preparation of RFP, assumptions and SOW for CROs and IP services vendors (labeling, packaging, distribution; IVRS/IWRS)</p></li><li><p>Provides input, reviews, and approves vendor study specifications for IP-related activities.</p></li><li><p>Serves as point of escalation for vendor-related IP issues as they arise.</p></li><li><p>May require 25% travel</p></li></ul><p>Staff Management</p><ul><li><p>May supervise staff.</p></li><li><p>May mentor or coach junior Clinical Drug Supply & Logistics staff.</p></li></ul><p>Process Initiatives</p><ul><li><p>Develops and implements process initiatives in accordance with business needs.</p></li></ul><p>Metrics</p><ul><li><p>Tracks metrics related to drug supply processes and staff.</p></li></ul><p>Training</p><ul><li><p>Provides assistance in training and development as needed.</p></li></ul><p>Reporting</p><ul><li><p>Compiles and reports supply status to study teams and senior management</p></li></ul><p>Problem solving</p><ul><li><p>Applies knowledge of company policies and standard practices to resolve problems.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>A minimum of Bachelors' degree and 8 years of relevant experience in the biotechnology/pharmaceutical industry, with 5 years minimum in clinical supply management.</p></li><li><p>Masters/MBA/PharmD with 5+ years of relevant industry experience. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Formulation Development (DPDT)]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49363]]></requisitionid>
    <referencenumber><![CDATA[R49363]]></referencenumber>
    <apijobid><![CDATA[r49363]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49363/principal-scientist-formulation-development-dpdt/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Principal Scientist</strong> to join our Drug Product Development & Technology (DPDT) team. You'll lead drug product development activities from candidate selection and pre-clinical development through clinical development and commercialization for a variety of drug modalities, which may include protein (antibody), siRNA, peptides, bioconjugates (antibody-oligo or antibody-drug), and AAV, across a variety of drug and delivery presentations including liquid and lyophilized DP and novel drug delivery technologies. You'll work independently to lead your project/program(s), applying biochemical, biophysical, and/or microbiology principles to execute both simple and complex experiments and processes.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours, with flexibility to support before- and after-hours executive meetings, town halls, and corporate events</li><li>Location: On-site in Tarrytown, NY</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Works independently and applies technical knowledge to design rigorous experiments that may include formulation, analytical, and process development and technology transfer</li><li>Acts as a resource and is recognized as a subject matter expert (SME) within their field; applies QbD approaches to drug product development and stays knowledgeable about current regulatory guidelines</li><li>Applies scientific and statistical knowledge of software packages (JMP or equivalent) to support study design and data analysis</li><li>Independently makes decisions of moderate complexity in a timely manner, including with limited information, understanding how decisions impact target priorities and cross-functional teams; uses a risk-based approach to make complex decisions and demonstrates judgment on when feedback from management is needed</li><li>Receives information and direction from leadership, and is responsible for planning and leading complex, long-term projects</li><li>Collaborates effectively as an SME and within cross-functional teams to support timely execution of deliverables</li><li>Proactively researches and implements new approaches toward problem-solving and/or process optimization for product development and new technology evaluations; capable of diving into novel fields and developing expertise needed in new areas or technologies</li><li>Brings managerial experience with demonstrated success developing direct reports; trains junior scientists in technical skills and mentors junior colleagues</li><li>Communicates effectively with varied audiences internally and externally, clearly explaining technical data that support recommendations or strategic direction</li><li>Participates in team meetings and prepares data presentations and documents, including publications and patents</li><li>Generates internal reports and authors external documents, which may include protocols, technical reports, risk assessments, regulatory documents, and patents</li><li>Maintains complete and accurate laboratory record documentation and complies with all data integrity procedures and system requirements, including ELN, SDMS, LIMS, and EDMS</li><li>Engages in lab and instrument maintenance activities, acting as instrument SME or team lead, and may champion implementation of new instrumentation and analytical techniques</li><li>Complies with environmental, health, and safety requirements</li></ul><h3><strong>This role requires:</strong></h3><ul><li>A PhD in Pharmaceutical Sciences, Biochemistry, Chemistry, Biophysics, Biomedical or Chemical Engineering, or a related field with 4+ years of relevant industry experience in the biopharma space; or a BS/MS with a minimum of 10 years, of relevant industry experience</li><li>Industry experience with bioconjugates, particularly antibody-oligonucleotide formulation development, is preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Nord (Ematologia)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49791]]></requisitionid>
    <referencenumber><![CDATA[R49791]]></referencenumber>
    <apijobid><![CDATA[r49791]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49791/key-account-manager-nord-ematologia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Costruiamo insieme il nostro futuro:</strong></p><p>In Regeneron utilizziamo la scienza e l’innovazione per sviluppare farmaci che cambiano la vita delle persone con malattie gravi. Cerchiamo un Senior Sales Specialist, Ematologia Commerciale, Italia da inserire nel nostro team vendite di ematologia. La posizione supporterà il business italiano con un modello di lavoro sul territorio. In questo ruolo, promuoverai la crescita del territorio e relazioni di valore con i professionisti sanitari. Collaborerai con i colleghi dell’area medica e con altre funzioni. Questa posizione offre l’opportunità di contribuire a un’organizzazione in rapida crescita, guidata dalla scienza e orientata ai pazienti.</p><p><strong>Quando e dove:</strong></p><p>Italia Nord<br>Posizione sul territorio, con trasferte frequenti.</p><p><strong>Scopri il tuo ruolo:</strong></p><ul><li><p>Costruire relazioni di qualità con i professionisti sanitari utilizzando conoscenze scientifiche aggiornate e messaggi di vendita approvati.</p></li><li><p>Attuare i piani commerciali e di marketing per raggiungere gli obiettivi di vendita e gli indicatori di performance.</p></li><li><p>Gestire gli account strategici attraverso pianificazione, targeting e segmentazione, in linea con le indicazioni regionali.</p></li><li><p>Sviluppare piani locali per gli account utilizzando dati di mercato e aggiornarli in base alle dinamiche del mercato.</p></li><li><p>Collaborare con i colleghi dell’area medica su programmi regionali a supporto delle esigenze dei professionisti sanitari.</p></li><li><p>Rappresentare Regeneron Ematologia in congressi e incontri regionali, nazionali e internazionali.</p></li><li><p>Utilizzerai canali diretti e digitali per ottimizzare il coinvolgimento e contribuire al miglioramento della pratica clinica.</p></li></ul><p><strong>Questo ruolo richiede:</strong></p><ul><li><p>Laurea o qualifica equivalente riconosciuta per i professionisti delle vendite.</p></li><li><p>Almeno cinque anni di esperienza nelle vendite farmaceutiche, inclusa un’esperienza essenziale in ematologia.</p></li><li><p>Conoscenza del Codice della Federazione Europea delle Industrie e Associazioni Farmaceutiche e delle normative locali applicabili.</p></li><li><p>Ottima conoscenza dell’italiano; la conoscenza dell’inglese costituisce un vantaggio.</p></li><li><p>Attitudine tecnica alla vendita basata sulla patologia e sui concetti scientifici.</p></li><li><p>Capacità di utilizzare dati, sistemi multipli e piattaforme di Customer Relationship Management.</p></li><li><p>Eccellenti capacità di coinvolgimento del cliente, presentazione, pianificazione e definizione delle priorità.</p></li><li><p>Capacità di lavorare autonomamente entro scadenze ristrette, dimostrando integrità e una comunicazione etica.</p></li><li><p>L’esperienza nel lancio di prodotti costituisce un vantaggio.</p></li></ul><p><strong>Salary Range (annually)</strong></p><p> € 59.325 - € 98.875</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-South Central]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47577]]></requisitionid>
    <referencenumber><![CDATA[R47577]]></referencenumber>
    <apijobid><![CDATA[r47577]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47577/regional-director-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the South Central Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: South Central (Texas and Louisiana)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Therapeutic Proteins]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49265]]></requisitionid>
    <referencenumber><![CDATA[R49265]]></referencenumber>
    <apijobid><![CDATA[r49265]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49265/associate-scientist-therapeutic-proteins/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a highly motivated, detail-oriented, and dependable Associate Scientist to join Therapeutic Proteins - Antibody Radioconjugates Technology, conjugating antibodies with bifunctional chelates and fluorescent probes, and radiolabeling conjugated antibodies to support preclinical immunoPET (iPET) and Cryo-fluorescence Tomography (CFT) imaging. You'll generate and characterize Zr-89 radiolabeled and fluorescently-conjugated tracers from our portfolio of antibodies and antibody-based therapeutics, enabling quantitative in vivo imaging studies across Oncology, Immuno-Oncology, and other therapeutic focus areas. Your work will directly enable same-day imaging studies that visualize biodistribution, tumor/tissue targeting, and pharmacokinetics of therapeutic candidates in preclinical models.</p><p><strong>When & where:</strong><br>Location: Tarrytown, NY - On-site</p><p><strong>Discover your role:</strong></p><ul><li>Performs bioconjugation of antibodies with bifunctional chelating agents (DFO, DOTA, etc.) and fluorescent probes following validated protocols</li><li>Characterizes antibody bioconjugates using SE-HPLC, SDS-PAGE, Western blot, and UV/Vis spectroscopy</li><li>Radiolabels bioconjugated antibodies with Zr-89, Cu-64, or other radionuclide isotopes; purifies radiolabeled products for same-day use in time-critical imaging studies</li><li>Runs quality control testing using radio-HPLC, radio-iTLC, and gamma counting to verify tracer quality before release</li><li>Maintains mammalian cell culture lines and performs cell-based assays to validate tracer binding and function</li><li>Coordinates tracer preparation timelines with imaging scientists and project teams across multiple therapeutic areas</li><li>Maintains detailed electronic laboratory notebooks and radiation safety records in compliance with regulations</li><li>Maintains instruments, troubleshoots instrumental/experimental problems, and orders/maintains supplies</li></ul><p><strong>This job might be for you if you:</strong></p><ul><li>Have hands-on experience with protein chemistry, bioconjugation, and chromatographic techniques; experience performing radiochemistry is a plus</li><li>Thrive in a collaborative, fast-paced environment where reliability and punctuality directly impact team success</li><li>Take pride in maintaining accurate, complete laboratory records</li><li>Excel at attention to detail and following established protocols with precision</li><li>Are self-motivated and eager to work independently after training</li><li>Have strong communication skills</li></ul><p><strong>This role requires:</strong></p><ul><li>B.S. in Chemistry, Biochemistry, Chemical Engineering, Chemical Biology, or a related field with 1-2 years of laboratory experience</li><li>Comfort working with radioactive materials and willingness to complete radiation safety training</li><li>Hands-on experience with protein chemistry and bioconjugation techniques, or strong foundational knowledge with willingness to learn</li><li>Experience with chromatographic techniques (HPLC, FPLC, or column chromatography) and mammalian cell culture</li><li>Proficiency with computers, data analysis software (Excel, Prism, or similar), and electronic laboratory notebook systems</li><li>Ability to lift 50 lbs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing – Eosinophilic Esophagitis (EoE)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49763]]></requisitionid>
    <referencenumber><![CDATA[R49763]]></referencenumber>
    <apijobid><![CDATA[r49763]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49763/associate-director-hcp-marketing-eosinophilic-esophagitis-eoe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director of HCP Marketing will lead healthcare professional omnichannel/non-personal promotions marketing strategy and execution as well as support execution of personal promotions marketing strategy for EoE in the US. This highly visible role requires a forward-looking individual with deep marketing expertise and the ability to navigate across cross-functional partners and complex alliance partnerships in a growing competitive market. The Associate Director will partner closely with cross-functional and alliance teams to advance product growth, contribute to the brand's financial success, and strengthen its leadership position in Gastroenterology and Allergy/Immunology. This position reports to the Director, EoE HCP Marketing.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY office 4 days a week</li><li>Must be willing to travel 25-30% (including weekend travel as needed)</li></ul><h3>Discover your role:</h3><ul><li>Lead HCP non-personal promotions/omnichannel marketing strategy, planning, and execution, ensuring full integration with the broader brand strategy.</li><li>Understand customer segmentation and strategies to build and implement metrics driven multi-channel plans for focused non-personal HCP engagements and optimal channel distribution.</li><li>Support execution of HCP personal promotions marketing strategy developing resources used by field sales team in HCP engagements.</li><li>Contribute to building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</li><li>Ensure all marketing programs align with corporate policies, regulatory/ethical frameworks, and alliance standards.</li><li>Drive strong cross-functional and alliance collaboration, alignment, and decision-making, partnering with Sales, Medical Affairs, TLLs, Market Research, Analytics, Market Access, Training, Regulatory, and Legal to deliver cohesive, compliant, and impactful initiatives.</li><li>Have a proven track record of leadership and influence across organizational levels.</li><li>Combine strategic and scientific competence with ability to translate insights into actionable marketing strategies.</li><li>Excel in execution and project management within a fast-paced dynamic environment, managing multiple projects simultaneously and working through ambiguity.</li><li>Bring exceptional communication and presentation skills, with the ability to simplify and convey complex strategies to diverse audiences—both technical and non-technical, including senior executives.</li><li>Demonstrate organizational agility, adapting priorities and strategies to external market shifts or internal dynamics.</li><li>Possess strong experience in managing agencies and external partners, ensuring creative excellence and accountability.</li><li>Disciplined in managing budgets and resources aligned to strategic objectives.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; MBA strongly preferred.</li><li>10+ years of progressive experience in the pharmaceutical/biotech industry or related field.</li><li>8+ years of US commercial experience in pharmaceutical/biotech marketing, product management, or related areas.</li><li>Gastroenterology/Allergy/Immunology biologics experience strongly preferred.</li><li>Demonstrated success in navigating complex alliance or co-promotion partnerships.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Quantitative Pharmacology]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49967]]></requisitionid>
    <referencenumber><![CDATA[R49967]]></referencenumber>
    <apijobid><![CDATA[r49967]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49967/associate-director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are seeking a highly motivated Associate Director (AD) to join the Quantitative Pharmacology (QP) group. The AD will lead model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies. This role combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.</p><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY, Cambridge, MA, Warren, NJ, Remote, USA</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making.</p></li><li><p>Leading the QP evaluation of one or more assets, accountable for timely delivery of population PK/PD, exposure–response, and translational modeling analyses.</p></li><li><p>Representing QP at program and governance meetings, communicating quantitative insights clearly to non-modeling audiences.</p></li><li><p>Contributing to regulatory interactions and authoring key components of regulatory documents related to QP (e.g., IB, briefing books, etc.).</p></li><li><p>Mentoring and developing junior scientists and fostering a culture of scientific rigor and collaboration.</p></li><li><p>Identifying and implementing process improvements, new modeling approaches, and innovative quantitative tools to enhance efficiency and impact.</p></li><li><p>Ensuring analyses and documentation are of the highest scientific quality and regulatory compliance.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field</p></li><li><p>6+ years of post-doctoral or industry experience; or MS with 9+ years of relevant experience.</p></li><li><p>Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.</p></li><li><p>Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA).</p></li><li><p>Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.</p></li><li><p>Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Fill Finish Production and Support]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49927]]></requisitionid>
    <referencenumber><![CDATA[R49927]]></referencenumber>
    <apijobid><![CDATA[r49927]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49927/manager-fill-finish-production-and-support/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manufacturing Support Operations Manager to join our IOPS team, providing direction and leadership to Production Manufacturing Support teams — including Cleaning Technicians and contracted Support Technicians — across our Fill and Finish areas. In this role, you will manage operations, contracts, and compliance across classified and iCNC spaces, while preparing and presenting metrics and reports that drive operational excellence. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Manage all aspects of Manufacturing Support operations across Fill and Finish areas, including oversight of full-time employees and contract staff; perform personnel management functions including evaluations, coaching, and disciplinary actions, with oversight and feedback to employer of record for contract employees</li><li>Own and manage contracts for contract labor and gowning providers; monitor and maintain inventory levels for all materials, supplies, and gowning in classified and iCNC spaces</li><li>Monitor cleaning schedules, progress, data, and work quality; analyze, interpret, and report assessment results, making recommendations to team members and leadership</li><li>Track industry trends to ensure the latest technologies and best practices are implemented regularly across manufacturing support operations</li><li>Draft and implement long-term planning for processes, staffing, and budget; develop and implement department policies and ensure effective administration in compliance with regulatory requirements</li><li>Prepare reports by collecting, analyzing, and summarizing operational information and trends; represent Manufacturing during regulatory inspections to respond to and address environmental, inventory, and material dispensing issues</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in a scientific/engineering discipline, or related field</li><li>Associate Manager: 6+ years of relevant cGMP manufacturing experience, and 3+ years of supervisory experience</li><li>Manager: 7+ years of relevant cGMP manufacturing experience, and 3+ years of supervisory experience</li><li>Senior Manager: B8+ years of relevant cGMP manufacturing experience, and 3+ years of supervisory experience</li><li>May consider equivalent combination of education and experience; level determined based on qualifications ​</li><li>Gowning and Physical Requirements: Role is performed in a cGMP classified manufacturing environment; gowning requirements apply per site SOPs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Integrated Data Quality]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50031]]></requisitionid>
    <referencenumber><![CDATA[R50031]]></referencenumber>
    <apijobid><![CDATA[r50031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50031/director-integrated-data-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, Integrated Data Review provides strategic leadership for the development, implementation, and continuous improvement of integrated data review processes across clinical programs. In partnership with Biostatistics and cross-functional collaborators, this role establishes scalable frameworks, standards, and oversight models to enable proactive, risk-based identification of data issues and ensure high-quality, inspection-ready clinical data. The position drives consistent execution of Data Review Plans and promotes adoption of integrated data review practices across study teams.</p><br><h3>When & where:</h3><ul><li>Location: Warren NJ, Armonk NY, and TarryTown NY</li><li>Work model/flexibility: on site 4 days a week</li><li>Travel percentage: 10%</li></ul><br><h3>Discover your role:</h3><ul><li>Define and lead the Integrated Data Review (IDR) strategy, including the implementation of an appropriate operating model, and governance framework across the portfolio.</li><li>Accountable for consistent execution, oversight, and critical issue of Data Review Plans (DRPs), and proactive identification of data quality risks.</li><li>Define minimum requirements and develop standardized data review plans methodologies, templates, processes, and guidance to enable consistent and effective execution across study teams.</li><li>Provide oversight of data review planes execution through established governance processes, KPIs, and quality metrics to ensure consistency, effectiveness, adherence to standards, and continuous improvement across programs.</li><li>Partner with the Clinical Data Reporting group to develop, implement, and maintain standardized libraries of data review outputs, including visualizations, listings, dashboards, and patient profiles, that support scalable and consistent execution of integrated data review processes across programs.</li><li>Collaborate with Quantitative Innovation and Statistical Strategy (QISS) team to translate Risk-Based Data Management (RBDM) methodologies into practical data review approaches and study-level requirements.</li><li>Proactively identify potential risks to data quality, integrity, and delivery timelines and implement mitigation strategies to ensure continuity, compliance, and successful delivery of departmental objectives.</li><li>Drive continuous improvement and innovation in IDR methodologies and technologies through analysis of metrics, lessons learned, inspection observations, and evolving industry practices.</li><li>Develop and maintain SOPs, work instructions, templates, and training materials using quality-by-design principles to support integrated data review processes.</li><li>Lead implementation, change management, and training initiatives to ensure consistent adoption.</li><li>Drive adoption of IDR methodologies across clinical and external data domains to support proactive issue detection and improved data quality outcomes.</li><li>Liaise with internal and external collaborators to develop strong relationships and ensure effective cross-functional collaboration and communication with respect to deliverables and throughout drug development process.</li></ul><br><h3>This role requires:</h3><ul><li>12+ years in Clinical Data Management within within the biotechnology, pharmaceutical or health related industry. With 5+ years of people management, leadership, and mentoring</li><li>Expert knowledge of clinical data management principles, processes, technologies and industry best practices.</li><li>Expert knowledge of integrated data review principles, data quality management, and critical-to-quality concepts.</li><li>Deep understanding of regulatory requirements and industry standards, including ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, and global data privacy regulations, with the ability to apply these in an operational setting.</li><li>Working knowledge of RBDM principles and their application to Integrated Data Review, including centralized monitoring activities.</li><li>Understanding of Risked Based Quality Management (RBQM) principles and their relationship to integrated data review and centralized monitoring.</li><li>Demonstrated experience establishing, implementing, and evolving integrated data review frameworks, governance models, and methodologies across clinical programs.</li><li>Experience identifying critical data and defining risk-based data review strategies.</li><li>Experience interpreting and analyzing clinical, operational, and external data to identify data trends and potential quality issues.</li><li>Experience developing, implementing, and overseeing Data Review Plans and associated governance processes.</li><li>Demonstrated ability to partner with cross-functional collaborators to support risk-based and integrated data review approaches.</li><li>Understanding of KPIs and quality metrics used to assess effectiveness and impact of integrated data review activities.</li><li>Demonstrated success in solving complex business problems through strategic and critical thinking.</li><li>Proven ability to lead and influence within a matrix organization, driving alignment and outcomes across cross-functional stakeholders without direct authority.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Rare Portfolio Marketing]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50048]]></requisitionid>
    <referencenumber><![CDATA[R50048]]></referencenumber>
    <apijobid><![CDATA[r50048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50048/director-us-rare-portfolio-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, US Portfolio Marketing, will be responsible for developing and driving comprehensive marketing strategies our rare disease portfolio: This role involves leading brand management efforts, engaging healthcare professionals (HCPs), reaching patients, caregivers, and the broader consumer audience directly to drive disease awareness, patient identification, and adoption of our therapies. Reporting to the franchise marketing head of the US Rare Disease Business Unit, this headquarters-based position will develop and implement brand strategies that align with company goals and address the unique needs of small, geographically dispersed rare disease patient populations, their caregivers, and the specialists who treat them.</p><p>Candidates should understand the US rare disease market — including the diagnostic odyssey, referral pathways, and specialty distribution and reimbursement dynamics that govern access — with the ability to effectively manage a commercial marketing team and provide strategic direction to the commercial field organization (i.e., Key Account Leads and Account Specialists). This requires the ability to demonstrate leadership in working with other members of the Regeneron account team; experience developing, monitoring, and completing account plans; and working with cross-functional partners in a collaborative and productive manner.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY Office 4 days a week</li></ul><h3>Discover your role:</h3><ul><li>Lead the brand planning process and facilitate quarterly business/brand reviews to evaluate key performance indicators and critical success factors</li><li>Define go-to-market strategies, evaluate competitive positioning, and drive launch planning and launch readiness activities</li><li>Design and implement patient-finding and HCP identification strategies against small, dispersed prescriber universes; drive direct-to-patient activation for products; partner on segmentation and targeting</li><li>Conduct market research and analyze data — including claims, diagnostic, specialty pharmacy/hub data, and patient and caregiver insights — to inform HCP and consumer marketing strategy</li><li>Develop content for HCP-focused promotional and educational materials across portfolio, including branded and unbranded disease-state platforms</li><li>Build and implement the consumer/DTC strategy — patient and caregiver campaigns, digital and social engagement, unbranded disease education, and patient testimonial and ambassador programs</li><li>Coordinate with external agencies for campaign development and execution</li><li>Partner with Patient Advocacy on relationships with patient organizations and the broader rare disease community</li><li>Shape the patient support and hub experience in partnership with Patient Support and Market Access to minimize time to therapy</li><li>Attend congresses and industry events to build the brand and establish KOL and community connections</li><li>Provide oversight of and collaborate with scientific marketing</li><li>Ensure cross-functional communication, alignment, and collaboration with Field Sales, Field Medical, Access and Reimbursement, Marketing, Legal, and Compliance</li></ul><h3>This role requires:</h3><ul><li>12 years of pharmaceutical or biotech experience with a focus on Marketing</li><li>Strong understanding of rare disease markets; experience with orphan drugs, specialty products, or advanced therapies is preferred.</li><li>We expect you to bring knowledge of the payer environment and challenges within National/Regional payer markets, including government programs, managed care, and evolving health care systems, as well as familiarity with buy-and-bill and/or specialty pharmacy channels.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Manager Benelux (Oncology)]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49979]]></requisitionid>
    <referencenumber><![CDATA[R49979]]></referencenumber>
    <apijobid><![CDATA[r49979]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49979/sales-manager-benelux-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regional Sales Manager, Oncology to join our international oncology organisation, supporting our HUB Markets in a remote role. In this role, you will lead sales teams and deliver business goals across multiple markets while collaborating with Marketing, Medical, Commercial Operations, and local partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Netherlands (Field)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead field sales and key account teams across multiple markets.</p></li><li><p>Coach and develop talent to achieve consistent sales performance.</p></li><li><p>Deliver national, regional, and local account plans against business goals.</p></li><li><p>Run cycle meetings and training using approved messages and materials.</p></li><li><p>Manage analytics, key performance indicators, incentives, and Veeva CRM processes.</p></li><li><p>Build trusted partnerships with customers, local partners, and cross-functional teams.</p></li><li><p>You adapt quickly, prioritise solutions, and remain steady across changing markets.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Extensive biopharma experience in international oncology sales management.</p></li><li><p>Proven leadership of field teams meeting or exceeding sales targets.</p></li><li><p>Field management experience and operational knowledge of sales technology.</p></li><li><p>Experience with CRM platforms and digital promotion activities.</p></li><li><p>Fluent English with strong leadership, planning, communication, and presentation skills.</p></li><li><p>A record of ethical, compliant sales performance and trusted stakeholder relationships.</p></li><li><p>Immuno-oncology experience and established oncology opinion-leader relationships are preferred.</p></li><li><p>Willingness to travel approximately 40%, including some weekends.</p></li><li><p>Proximity to an international airport is advantageous.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€93,000.00 - €155,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Process Controls & Validation Engineer]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49085]]></requisitionid>
    <referencenumber><![CDATA[R49085]]></referencenumber>
    <apijobid><![CDATA[r49085]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49085/sr-process-controls-validation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Process Controls & Validation Engineer with a strong background in cGMP validation, who can develop sound process control strategy, bring structure to ambiguous technical problems, and confidently lead and influence discussions across Manufacturing, Quality and Regulatory teams. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering and mathematical needs from the laboratory to the manufacturing floor. This role provides technical support to our bulk manufacturing, quality and CMC Regulatory for manufacturing processes from technology transfer and/or design transfer to post-commercial lifecycle management activities.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work Schedule: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Leads and provides hands-on support for cGMP process validation (Stage 1–3), technology transfer, design transfer, scale-up, and process control strategy development, from protocol authoring through execution and lifecycle management—translating ambiguous, early-stage problems into clear, actionable plans with limited direction</li><li>Evaluates product/process risk and applies engineering judgment to resolve gaps and uncertainty as processes move from development to at-scale manufacturing</li><li>Analyzes data across the process lifecycle—from development through characterization and manufacturing history—using statistics and engineering principles to inform control strategy, validation decisions, and identify critical process parameters, control limits, and monitoring plans</li><li>Leads and influences cross-functional discussions with Manufacturing, Quality Control, Quality Assurance, and CMC Regulatory, driving alignment and decisions on process lifecycle management, and effectively navigating differing stakeholder priorities</li><li>Authors protocols, reports, and technical documents grounded in available process/product knowledge; ensures SOPs, policies, and validation plans align with industry/regulatory expectations (e.g., ICH); supports audits/inspections and CMC sections of regulatory submissions as needed</li><li>Provides hands-on support for laboratory and manufacturing-scale studies, working effectively in a team-oriented environment</li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering; chemical engineering or biomedical engineering preferred <ul><li>Process Controls & Validation Engineer: 2+ years of experience</li><li>Sr. Process Controls & Validation Engineer: 5+ years of experience</li><li>Level will be determined based on experience</li></ul></li><li>Experience with process validation, tech transfer and scale up for drug substance </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Medical Affairs Operations, France]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49885]]></requisitionid>
    <referencenumber><![CDATA[R49885]]></referencenumber>
    <apijobid><![CDATA[r49885]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49885/manager-medical-affairs-operations-france/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Manager, Medical Affairs Operations, France</h3><p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager, Medical Affairs Operations, France</strong> to join our Medical Affairs team in France, supporting our country organisation in a hybrid work mode. In this role, you will deliver compliant country Medical Affairs activities while collaborating with local Medical Affairs colleagues and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When</strong> <strong>&</strong> <strong>where:</strong> Paris, office-based - Hybrid</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Maintain audit readiness through documentation, tracking, and records management.</li><li>Optimise transparency reporting, Anti-Bribery and Anti-Corruption documentation, and compliance processes.</li><li>Complete assigned medical activities in local systems through regulatory and GxP completion.</li><li>Localize global, regional, and local standard operating procedures and work instructions.</li><li>Handle vendor onboarding, contracts, purchase orders, budgets, and expense reconciliation.</li><li>Coordinate medical meetings, congress logistics, agenda flow, actions, and follow-up.</li><li>You bring structure and service focus to cross-functional Medical Affairs operations.</li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>Bachelor’s degree in life sciences, business, or a related field, or equivalent experience.</li><li>7+ years in Medical Affairs operations, coordination, project support, or administration.</li><li>Pharmaceutical or biotech environment experience.</li><li>Experience in a country organization or local operating company.</li><li>Solid understanding of compliance, transparency, and regulated country-level processes.</li><li>Fluency in French, with business-proficient English preferred.</li><li>Microsoft Office and relevant systems experience, including Veeva CRM, Vault Medical, PromoMats, and procurement tools.</li><li>Occasional business travel as required.</li><li>Country Medical Affairs operations experience, including event and congress planning.</li><li>Contract and procurement systems knowledge, such as iCertis or SAP.</li><li>Experience partnering with Finance and Procurement teams.</li><li>Commercial operations experience desirable.</li><li>Strong organization, communication, stakeholder management, and cross-functional collaboration skills.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€60,750.00 - €101,250.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manufacturing Scheduling Specialist]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49860]]></requisitionid>
    <referencenumber><![CDATA[R49860]]></referencenumber>
    <apijobid><![CDATA[r49860]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49860/manufacturing-scheduling-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Manufacturing Scheduling Specialist</strong> to join our <strong>Supply Chain Planning </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Providing daily, weekly and monthly schedules to enable production to meet plan</li><li>Assisting in the coordination of scheduling activities with both manufacturing and non-manufacturing groups</li><li>Providing the BPS with the appropriate level of detail in order to complete the job safely</li><li>Facilitating the daily Planning and Scheduling meetings with Manufacturing and supporting functions</li><li>Acting as the principle liaison between Maintenance, Process Utilities, Engineering, and Manufacturing to complete maintenance and repair activities</li><li>Initial screening of incoming work orders, priority of job, identification of scope, and analysis of the required level of planning</li><li>Performing data collection and analysis related to process durations, operator efficiencies, and characterizing scheduling delays</li><li>Creating data models using spreadsheets, code, or other relevant methods</li><li>Assisting in capacity planning decisions</li><li>Assisting in improving communication between different shifts, process areas, and levels of the organization</li><li>Assisting with the creation of scheduled start-up & shutdown project plans</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You thrive in a multifaceted and fast-paced environment</li><li>You can handle and prioritise multiple tasks and requests simultaneously</li><li>You are detail oriented and proactive with excellent time management skills</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Requires a BS/BA in Science, Engineering or a related field (MS in similar field preferred) and 2 years experience in a related area.</li></ul><h3>Thrive today. Grow tomorrow.</h3><p><strong>#IRELIM #JOBSIEST #LI-Onsite </strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist (Overnights)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46370]]></requisitionid>
    <referencenumber><![CDATA[R46370]]></referencenumber>
    <apijobid><![CDATA[r46370]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46370/associate-biotech-production-specialist-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Biotech Production Specialist to join our Global Manufacturing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.</p><div><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: 3rd shift, 10pm-8:30am with the potential for 1-2 weekend days</p></li><li><p>Other requirements: Occasional flexibility may be requested for on-call schedule/weekend work</p></li></ul><p><strong>What you'll do:</strong></p><ul><li><p>Cover all facets of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Complete and review batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Perform in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operate automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Support equipment start-up, troubleshooting, and validation</p></li><li><p>Partner with R&D teams to implement new drug manufacturing processes and technologies</p></li><li><p>Work in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients</p></li><li><p>Operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients</p></li><li><p>Use computerized systems for daily performance of tasks</p></li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li><p>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p><strong>Let's find out if we're a fit:</strong></p><ul><li><p>HS diploma + 4 years of relevant work experience is required</p></li><li><p>Or AS, BS or BA in Life Sciences or related field</p></li><li><p>Level will be determined based on experience</p></li></ul><p><strong>Thrive today. Grow Tomorrow.</strong></p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family care benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[PharmD Program Associate - Clinical Sciences]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50223]]></requisitionid>
    <referencenumber><![CDATA[R50223]]></referencenumber>
    <apijobid><![CDATA[r50223]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50223/pharmd-program-associate-clinical-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles.</p><p>This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas.</p><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY</p></li><li><p><strong>Travel percentage:</strong> Up to 15%</p></li></ul><p><strong>Program Tracks:</strong><br>The program is comprised of a 24-month rotational experience within one of the following tracks:</p><ul><li><p>Clinical Operations & Program Management</p></li><li><p><strong>Clinical Sciences</strong></p></li><li><p>Regulatory Strategy</p></li><li><p>Regulatory Labeling & Advertising/Promotion</p></li><li><p>Safety Sciences</p></li></ul><p>Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program.</p><p><strong>Clinical Sciences:</strong> Associate will participate in clinical activities throughout the lifetime of a drug development program, driving development programs from pre-IND/IND stage through completion of pivotal trials. The Clinical Scientist associate will participate in clinical studies that could range across clinical experimental sciences studies, early/late phase clinical trials and post-marketing requirement studies.</p><p><strong>Discover your role:</strong></p><ul><li><p>Drafting documents integral to clinical sites and regulatory submissions</p></li><li><p>Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others</p></li><li><p>Managing third-party vendors and maintaining timelines of key results</p></li><li><p>Developing regulatory strategies for clinical development programs</p></li><li><p>Analyzing safety data to characterize the safety profile of products throughout their development lifecycle</p></li><li><p>Working with program mentors to improve skills to reach professional goals better</p></li><li><p>Opportunities to travel to clinical sites and/or meetings with health authorities</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates within a life science related area of study may also be considered.</p></li><li><p>You must have completed your PharmD and/or PhD degree by Summer 2027</p></li><li><p>Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus</p></li><li><p>Exposure or familiarity with evaluating clinical trials, scientific literature and data </p></li><li><p>You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences</p></li><li><p>You are eligible to work in the U.S. on a permanent basis</p></li></ul><p><strong>Application Details:</strong></p><p><strong>When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference.</strong></p><p><strong>Applications Accepted: August 24th, 2026 - September 11th, 2026</strong><br>For more information on the tracks, program, and interview process, please refer to the brochure.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49788]]></requisitionid>
    <referencenumber><![CDATA[R49788]]></referencenumber>
    <apijobid><![CDATA[r49788]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49788/executive-assistant/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we pair science with technology to accelerate the discovery and delivery of life-changing medicines. We are seeking an Executive Assistant to support Law Department executives who oversee and collaborate with multiple functional teams, attorneys, and professionals across the organization. This role requires a strong understanding of the Law Department, its business clients, and the key relationships that enable the team to operate effectively. We are looking for someone who brings strategic thinking, technological fluency, sound judgment, and genuine curiosity to the work of a fast-moving, high-impact legal function.</p><p>The Executive Assistant will exercise considerable judgment and initiative, influence stakeholders, and anticipate the needs of senior leaders and their teams. The position will report to a Vice President/Associate General Counsel and support two additional Vice Presidents, one Senior Vice President, and approximately 15 additional lawyers.</p><p><strong><em>This role will require 4 days per week onsite at our HQ Campus in Sleepy Hollow, NY. This is not available as a fully remote / hybrid role.</em></strong></p><p><strong>A typical day might include the following:</strong></p><p><strong>This role may be for you if you have the following:</strong></p><ul><li>Are highly collaborative and adept at coordinating across teams to develop and implement solutions and operate under minimal guidance.</li><li>Exhibit discretion, independence, and sound judgment.</li><li>Adapt well to change, ambiguity, and shifting priorities, and can embrace AI and modern productivity tools as a part of how you work.</li><li>Work comfortably with senior leaders and understand how they think and what they expect.</li><li>Excellent interpersonal and oral and written communication skills, with a proven ability to collaborate seamlessly across cross-functional teams, senior leaders, and fellow administrative coordinators</li><li>Advanced technology skills, including proficiency in PowerPoint, Excel, SharePoint, Word, Outlook, and Adobe Acrobat Pro; hands-on experience leveraging AI tools such as Copilot and to streamline workflows and improve team efficiency</li><li>Ability to prioritize – strong organizational, planning, and project management skills are vital</li><li>Experience utilizing travel software and preparing expense reports - Concur preferred</li><li>Possess advanced knowledge or ability to readily learn company and Law Department policies, practices, and resources and act as a point person for supported leaders and departments.</li><li>Proactively identify opportunities for continuous improvement to current processes.</li><li>Communicate exceptionally well, whether orally or in writing.</li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li>Associate or bachelor’s degree preferred.</li><li>Eight or more years of administrative experience required, with at least four years supporting senior leaders in a business or legal environment.</li><li>Advanced proficiency in Microsoft 365 (Outlook, PowerPoint, Excel, Word, Teams), SharePoint, Concur, and collaboration platforms; ability to troubleshoot and train others.</li><li>Proven ability to manage complex calendars, orchestrate senior‑level meetings and events, and coordinate domestic/international travel with precision.</li><li>Exceptional organization, prioritization, and follow‑through; positive, can‑do attitude and respect for colleagues at all levels.</li><li>Flexibility to support after‑hours needs tied to executive travel, global time zones, and critical events.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$33.80 - $52.93]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 10:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Supply Strategy and Innovation]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49864]]></requisitionid>
    <referencenumber><![CDATA[R49864]]></referencenumber>
    <apijobid><![CDATA[r49864]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49864/senior-director-supply-strategy-and-innovation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director of Supply Strategy and Innovation to lead our Supply Chain Center of Excellence, developing and executing the supply chain strategic roadmap across IOPS global manufacturing and distribution networks. In this role, you will set long-range strategic vision while providing hands-on leadership for daily execution — transforming supply chain processes, overseeing planning technology and data, and driving alignment across clinical and commercial portfolios — while partnering with IT/OT, Finance, CMC Program Management, Commercial, R&D, and Manufacturing.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model/flexibility: Monday–Friday, 8:00am–4:30pm</li><li>Travel percentage: Some business travel required</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop, implement, and continuously evolve the Center of Excellence's long-range strategy and roadmap, integrating with supply chain and business processes including S&OP, and translating strategy for stakeholders at every level</li><li>Build strategic and tactical alignment with cross-functional partners including IT/OT, IOPS PMO, Finance, CMC Program Management, Regulatory Sciences, Commercial, R&D, Procurement, and Manufacturing to ensure unified objectives and accountability to delivery</li><li>Own the supply chain project portfolio, driving performance and accountability against project milestones; lead change management activities and adoption across suppliers, customers, and end users</li><li>Guide the utilization and evolution of advanced planning and analytics tools including ERP/MRP/APS systems; own supply chain master data and integrate into enterprise governance; partner with IT/OT leadership to define the digital roadmap for planning systems</li><li>Champion continuous improvement initiatives that transform business processes, reduce lead times, manage costs, and enhance end-to-end supply chain efficiency</li><li>Develop and trend KPIs; evaluate the financial and operational impact of strategic projects and engage leadership to identify opportunities that improve efficiency while minimizing cost</li><li>Lead, mentor, and develop a high-performing team, fostering a culture of accountability, agility, and data-driven decision-making</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Business, Engineering, Supply Chain Management, or a related field; advanced degree preferred</li><li>Senior Director: 15+ years of progressive experience in the same; level determined based on qualifications</li><li>Deep expertise in demand planning, supply planning, and supply chain management concepts; strong command of ERP/MRP/APS systems and planning analytics required</li><li>Demonstrated experience developing and executing long-range supply chain strategy, ideally within a Center of Excellence or similarly matrixed organization</li><li>Experience in a cGMP environment with a strong understanding of regulatory requirements preferred</li><li>Relevant certifications a plus including PMP, APICS, ISM, ASQ, CPIM, CSCP, CPSM, CSSBB, or Lean Six Sigma</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Applications Analyst, QC Lab Systems]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49168]]></requisitionid>
    <referencenumber><![CDATA[R49168]]></referencenumber>
    <apijobid><![CDATA[r49168]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49168/senior-it-applications-analyst-qc-lab-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior IT Applications Analyst — QC Lab Systems to join our IOPS IT team, supporting the configuration, implementation, and ongoing management of IT QC Lab applications and systems. In this role, you will serve as a technical SME and business-facing partner — driving system enhancements, ensuring GxP compliance, and acting as the primary integration point between QC, IT, automation, and external vendors — while collaborating with Quality, Validation, and laboratory stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick County</li><li>Work model/flexibility: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Acting as Technical SME and lead on QC Lab IT application initiatives, coordinating across business departments to gather, prioritize, and implement system enhancement requests</li><li>Owning IT Applications change control processes including converting User Requirement Specifications to Detail Design Specifications, writing configuration test plans, and producing summary reports</li><li>Applying working knowledge of 21 CFR Part 11 across GxP computerized systems; identify and remediate compliance gaps and participate in regulatory audits and inspections</li><li>Acting as the primary integration point between QC, IT, automation, and external vendors; evaluate vendor platforms and integration tools for orchestration capabilities and lead technical discussions with system integrators and software suppliers</li><li>Partnering with Validation and Quality teams to ensure IT applications are implemented following a compliant development lifecycle approach</li><li>Configuring tabular, trend, and label reports; lead system security access reviews and periodic audit trail assessments; provide on-the-floor guidance and application-level troubleshooting for end users</li><li>Prioritizing day-to-day work assignments for analysts within the IT department to support application troubleshooting activities; train IT Applications team members and maintain up-to-date training records for self and direct reports</li><li>Supporting and maintain systems built on cloud and/or hybrid architectures in alignment with lab instrument connectivity and data flow requirements</li><li>Workinging knowledge of 21 CFR Part 11 and GxP computerized system compliance; experience participating in regulatory audits and inspections preferred</li><li>Understanding of lab instrument connectivity and data flows</li><li>Experience with cloud and/or hybrid architectures (AWS, Azure, or similar) preferred</li><li>Project management experience; professional qualification preferred</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology or a related field with a minimum of 5 years of relevant experience, or equivalent combination of education and experience</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs Hematology Austria]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49862]]></requisitionid>
    <referencenumber><![CDATA[R49862]]></referencenumber>
    <apijobid><![CDATA[r49862]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49862/senior-manager-field-medical-affairs-hematology-austria/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Field Medical Affairs Hematology Austria to join our Medical Affairs team, supporting our hematology business area in a field-based work mode. In this role, you will drive scientific exchange, generate field insights, and support research initiatives while collaborating with key opinion leaders, healthcare professionals, investigators, and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Austria - Field-based</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Build and maintain engagement plans with medical experts and investigators.</li><li>Establish scientific relationships with key opinion leaders in hematologic malignancies.</li><li>Act as a clinical and scientific resource on disease state information.</li><li>Support company-sponsored studies through investigator selection, site initiation, and enrolment activities.</li><li>Advance investigator-initiated study concepts with investigators and Medical Affairs partners.</li><li>Identify medical insights, research gaps, and collaboration opportunities.</li><li>Present scientific and clinical data compliantly to healthcare professionals and researchers.</li><li>You bring external insights that help shape medical strategy and priorities.</li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>PhD, PharmD, MD, or Doctor of Veterinary Medicine (DVM).</li><li>4+ years of relevant experience, including 2+ years as a Medical Science Liaison in hematology.</li><li>Knowledge of hematology; lymphoma and/or multiple myeloma experience preferred.</li><li>Understanding of treatment guidelines, clinical research processes, EU regulations, and compliant practices.</li><li>Ability to communicate complex scientific data and engage as a scientific peer.</li><li>Established relationships with hematology key opinion leaders and relevant institutions preferred.</li><li>Experience supporting cross-functional collaboration within a matrix pharmaceutical environment.</li><li>Ability to identify opportunities, tackle problems, manage priorities, and work independently.</li><li>Strong written and verbal communication skills with audience-focused communication.</li><li>Experience balancing field activities and project participation.</li><li>Proficiency with word processing, presentations, and spreadsheet applications.</li><li>Valid driver’s license, clean driving record, and ability to travel approximately 80%, including overnight travel.</li><li>Fluency in German and English.</li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€103,425.00 - €172,375.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Medical Affairs Hematology  - Austria]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49861]]></requisitionid>
    <referencenumber><![CDATA[R49861]]></referencenumber>
    <apijobid><![CDATA[r49861]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49861/director-medical-affairs-hematology-austria/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director Hematology Medical Affairs Austria to join our Medical Affairs team, supporting our hematology business area in a hybrid work mode. In this role, you will provide scientific and medical leadership, shape medical strategy, and advance clinical and medical initiatives while collaborating with Medical Affairs, Clinical Sciences, Regulatory, Commercial, Market Access, and external experts. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Austria & Fieldbased</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Serve as the in-country medical lead for hematology programs and scientific initiatives.</li><li>Represent Medical Affairs in cross-functional planning with regional, international, and headquarters teams.</li><li>Lead and develop the hematology medical team through mentoring, hiring, training, and performance management.</li><li>Support clinical development through investigator engagement, site identification, and research activities.</li><li>Deliver scientific presentations to physicians, pharmacists, and other healthcare partners.</li><li>Partner with field medical teams on congresses, symposia, advisory boards, and medical content.</li><li>Provide medical input to commercialization, market access, launch readiness, and lifecycle strategies.</li><li>You build positive relationships and bring actionable insights that strengthen patient-focused decision making.</li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>MD or PhD with hematology expertise and significant pharmaceutical or biotechnology Medical Affairs experience.</li><li>Recent multiple myeloma experience and a well-established network of clinical experts.</li><li>Solid understanding of Medical Affairs practices and applicable country codes of conduct.</li><li>Experience supporting clinical research and clinical development, preferably in hematology.</li><li>Understanding of the local healthcare environment and product lifecycle development.</li><li>Ability to identify strategic Medical Affairs opportunities and optimize planning.</li><li>Proven success working across matrix and cross-functional organizations.</li><li>Ability to build credibility with internal stakeholders, key opinion leaders, and external experts.</li><li>Strong leadership, mentor, and people management capabilities.</li><li>Excellent scientific communication skills with the ability to deliver strategic, actionable insights.</li><li>Ability to manage multiple projects independently while maintaining compliance standards.</li><li>Fluency in English and German.</li><li>Ability and willingness to travel 30-50%.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€121,800.00 - €203,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Engineering Technician]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49953]]></requisitionid>
    <referencenumber><![CDATA[R49953]]></referencenumber>
    <apijobid><![CDATA[r49953]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49953/engineering-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Engineering Technician to join our Process Sciences Drug Product Engineering department. This role works in a medical device laboratory and/or machine shop to perform testing and development activities defined by the Combination Products Applied Research group. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>What you’ll do: </strong></p><ul><li>Maintains, troubleshoots and repairs laboratory and/or machine shop equipment</li><li>Assists with maintenance of laboratory/machine shop supplies and testing materials</li><li>Provides subject matter expertise for operation and proper application of laboratory and/or machine shop equipment</li><li>Develops test methods for testing of combination products</li><li>Authors operator instructions and logbooks</li><li>Assists with equipment qualification including preparation of system requirements and IQ/OQ development</li><li>Performs feasibility testing, test method validation and design verification and inspection for combination products</li><li>Authors reports detailing results of testing</li><li>Documents deviations, performs investigations and implements corrective/preventive actions</li><li>Assists with combination product, assembly and test equipment development</li><li>Follows current good manufacturing practices (cGMPs)</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>Requires a BS/BA in an engineering field; or equivalent combination of education and experience<ul><li>Engineering Technician I: 0-2 years of experience</li><li>Engineering Technician II: 2+ years of experience</li><li>Level will be determined based on experience</li></ul></li><li>Experience in a cGMP environment preferred.</li><li>Experience with mechanical, electrical and/or functional laboratory testing preferred</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.49 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Oracle Fusion ERP Deployment Lead]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50016]]></requisitionid>
    <referencenumber><![CDATA[R50016]]></referencenumber>
    <apijobid><![CDATA[r50016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50016/executive-director-global-oracle-fusion-erp-deployment-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is a leading biotechnology company built on a simple but powerful mission: to use the power of science to bring new medicines to patients, over and over again. Founded and led by physician-scientists, we've turned that mission into one of the industry's most productive pipelines, nearly all of it homegrown in our own laboratories, powered by proprietary technologies like our VelociSuite® platform. From Dupixent and EYLEA to a rapidly expanding portfolio across oncology, cardiovascular and metabolic disease, neuroscience, and rare disease, our science is reaching millions of patients worldwide, and we're just getting started.</p><p>As we invest billions in new manufacturing capacity, expand our global footprint, and build the next generation of digital and technology capabilities to match the scale of our ambition, Regeneron offers a rare combination: the resources and reach of an industry leader, paired with the energy, curiosity, and relentless focus on invention of a company still writing its next chapter. This is a place where technology doesn't just support the business, it accelerates the science that changes patients' lives.</p><p><strong>Role Description</strong></p><p>Regeneron is making the largest technology investment in its history through a global Oracle Fusion Cloud deployment that will serve as the enterprise platform for finance, planning, manufacturing, and operations worldwide. The Executive Director, Oracle Fusion Global Lead will be accountable for the end-to-end technology delivery of this transformation, from strategy and design through implementation, stabilization, and ongoing optimization. This leader will drive the modernization of Regeneron's operating model, including evaluating the insourcing of key capabilities and integrating support from the company's Global Capability Center in India. As the technology owner of the program, they will shape platform strategy, oversee enterprise-wide execution, and serve as the primary Digital & Technology representative to senior stakeholders, vendors, and delivery partners.</p><p><strong>What You'll Lead</strong></p><ul><li>Own the global Oracle Fusion Cloud strategy, roadmap, and investment priorities, ensuring alignment with corporate objectives and enterprise performance goals.</li><li>Lead end-to-end delivery of the Oracle Fusion transformation, accountable for the ERP business case, budget, governance, milestones, stakeholder alignment, and deployment execution through stabilization.</li><li>Direct a global organization of employees and contractors, driving talent development, resource planning, organizational effectiveness, and a culture of accountability and execution excellence.</li><li>Establish enterprise standards for application integration, data management, analytics, AI, and platform governance, creating a scalable foundation for future Regeneron technology platforms.</li><li>Partner with Finance, Manufacturing, Procurement, HR, and other business leaders to align Oracle Fusion capabilities with operational priorities and measurable business outcomes.</li><li>Modernize and standardize global business and technology operations by simplifying workflows, improving data quality, enhancing reporting and analytics, advancing AI-enabled automation, and aligning global operating models across regions, shared services, and the GCC.</li><li>Evaluate and execute opportunities to internalize strategic capabilities, while managing strategic vendors, implementation partners, managed services, contracts, and technology spend to ensure delivery quality and financial discipline.</li><li>Ensure long-term platform success through SOX-compliant operations, financial systems support (ERP/EPM), release governance, data and integration standards, and ownership of value realization against the approved ERP business case.</li></ul><p><strong>What You Bring</strong></p><ul><li>BS/BA in Computer Science, Information Systems, or a related field required; MS or MBA preferred.</li><li>17+ years of progressive enterprise applications leadership, including large-scale Oracle Fusion Cloud (ERP/EPM/HCM) programs at global scale; experience leading a program of similar magnitude to Regeneron's largest-ever technology investment is strongly preferred.</li><li>Proven experience leading global, multi-year ERP transformation programs, including program governance, business case development, value realization, and cross-functional delivery.</li><li>Experience designing and integrating global operating models that incorporate a Global Capability Center (GCC) or similar offshore/nearshore delivery model spanning both business and technology operations.</li><li>Track record evaluating build-vs-buy and insourcing/outsourcing decisions for strategic technology and business process capabilities.</li><li>Preferred to have deep expertise in Oracle Fusion architecture, release strategy, and integrations. Outstanding leaders with a strong history of success with SAP implementations may be considered.</li><li>Hands-on, current knowledge of Oracle Fusion Cloud technologies, including recent platform releases, embedded AI/ML capabilities, and evolving analytics and integration tooling, is a plus.</li><li>Proven ability to lead global teams, negotiate complex matters, set standards across functional areas, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, Neurology]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50235]]></requisitionid>
    <referencenumber><![CDATA[R50235]]></referencenumber>
    <apijobid><![CDATA[r50235]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50235/senior-medical-director-medical-affairs-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Neurology/Myasthenia Gravis Medical Affairs Team. The Senior Medical Director is responsible for the co-development of medical strategy and planning & execution of medical affairs activities at Regeneron. This hire will provide medical leadership and serve as a key scientific/medical resource. The Senior Medical Director will report to Head of Medical Affairs, Neurology and work in a cross-functional, matrix organization. He/she will also collaborate with external stakeholders such as healthcare practitioners, key opinion leaders and payers.</p><p><strong>When & Where:</strong></p><p>Location: Sleepy Hollow, New York; Warren, New Jersey; or Cambridge, Massachusetts</p><p><em>*If hired in Warren, NJ or Cambridge, MA frequent travel to Sleepy Hollow, MA may be required*</em></p><p><strong>Discover your role:</strong></p><ul><li><p>You maintain deep scientific and medical knowledge of Neurology / Myasthenia Gravis, treatment landscape and clinical decision making</p></li><li><p>undefined</p></li><li><p>You function as an integral member of the cross-functional Medical Team</p></li><li><p>You are responsible for data generation, data analyses and interpretation as it relates to Phase 4 studies, including interventional and observational research</p></li><li><p>undefined</p></li><li><p>You are responsible for the medical content of post-marketing study reports, analyses of clinical data, safety monitoring, and activities that ensure patient safety</p></li><li><p>You provide scientific and medical support for development of strategic medical, publications, communications and integrated evidence generation plans</p></li></ul><ul><li><p>You participate in developing and presenting medical content at congresses, symposia and advisory boards</p></li><li><p>undefined</p></li><li><p>You proactively bring patients' & physicians' voice on cross-functional teams, to enable effective and impactful decision making</p></li><li><p>You provide medical training for internal staff on investigational and/or approved products, disease state and unmet needs</p></li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li><p>MD or equivalent with board eligibility/board certification in Neurology with a minimum of 10 years of relevant experience and 5+ years of Medical Affairs experience in Pharma/Biotech</p></li><li><p>PhD or PharmD with a minimum of 12 years of relevant experience and 8+ years of Medical Affairs experience in Pharma/Biotech</p></li><li><p>Direct experience in Myasthenia Gravis or Neurology Rare Disease, and prior launch experience is strongly preferred</p></li><li><p>Experience and ability in working in a dynamic, matrix environment; excellent collaboration and communication skills</p></li><li><p>undefined</p></li><li><p>Ability to demonstrate deep understanding of all medical affairs accountabilities</p></li><li><p>undefined</p></li><li><p>Thorough understanding of Neurology and Myasthenia Gravis healthcare environment and key stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology (NYC and NJ)]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50182]]></requisitionid>
    <referencenumber><![CDATA[R50182]]></referencenumber>
    <apijobid><![CDATA[r50182]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50182/associate-director-field-medical-affairs-hematology-nyc-and-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where: </strong>Territory: NYC (all boroughs) and NJ<br>Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. <br> </p><p>#medicalscienceliaison #msl #HFM #AD</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (f/m/d) - Nürnberg - Erlangen - Würzburg - Aschaffenburg]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49972]]></requisitionid>
    <referencenumber><![CDATA[R49972]]></referencenumber>
    <apijobid><![CDATA[r49972]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49972/sales-specialist-oncology-fmd-nuernberg-erlangen-wuerzburg-aschaffenburg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist Oncology (f/m/d) to represent our Oncology division across the Nürnberg - Erlangen - Würzburg - Aschaffenburg territory. In this role, you will build strong relationships with Healthcare Professionals (HCPs), identify key opinion leaders, and tailor your approach to individual and account needs, all in service of bringing our Oncology portfolio to the patients who need it. This is an opportunity to bring a "patient first" mindset to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><br><p><strong>Where:</strong></p><p>Field-based in Nürnberg - Erlangen - Würzburg - Aschaffenburg territory</p><br><p><strong>Discover your role:</strong></p><ul><li>Establish and lead high-quality HCP interactions by keeping your scientific knowledge of the product, indication, and brand sales messaging current, and reliably implementing sales & marketing plans</li><li>Consistently deliver on the brand's value proposition, ensuring objectives are met through clear key message communication to HCPs</li><li>Manage your territory with professional account planning, applying a targeting & segmentation approach aligned with regional and country-level guidance</li><li>Develop and implement a local account plan grounded in key data sources and local market insights, in line with the Germany Brand Plan</li><li>Collaborate closely with medical colleagues to implement regional programmes and activities that support HCP needs</li><li>Leverage all communication channels, including digital, in collaboration with other functions, to achieve the best possible share of voice in the market</li><li>Report results and developments proactively and clearly to the Germany leadership team</li></ul><p><br> </p><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree or equivalent experience, plus a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech / pharmaceutical sector, including experience in Oncology</li><li>Proficiency in German, plus conversational English</li><li>A deep understanding of the local healthcare economy, with the ability to identify key players in Oncology</li><li>A "patient first" value system</li><li>Readiness for very frequent travel and a Class 3/B driver's licence</li></ul><br><p><br>Salary range (annually)</p><p>73,125 -121,875 €</p><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48463]]></requisitionid>
    <referencenumber><![CDATA[R48463]]></referencenumber>
    <apijobid><![CDATA[r48463]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48463/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Dublin, Ireland</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€172,500.00 - €288,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, R&D Chemistry, Peptidomimetics]]></title>
    <date><![CDATA[Tue, 16 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48138]]></requisitionid>
    <referencenumber><![CDATA[R48138]]></referencenumber>
    <apijobid><![CDATA[r48138]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48138/associate-director-rd-chemistry-peptidomimetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director (Peptidomimetics), R&D Chemistry</strong></p><p>We are currently seeking an established leader and drug hunter for the R&D (Research & Development) Chemistry group. In this position, they will play a key role in expanding the Regeneron peptidomimetic antibody-conjugate drug discovery capabilities, while providing innovation and leadership to seamlessly combine with the company’s existing expertise in biologics and novel genetic medicines. The candidate will drive the discovery of peptidomimetic antibody conjugate drug therapeutics across diverse research areas. Cultural fit with the Regeneron cross-functional teams will be a key driver for success. </p><p>The R&D Chemistry team is primarily composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have a peptidomimetic/synthetic organic/medicinal chemistry background and will require peptidomimetic synthesis, discovery and SAR (structure-activity relationship) optimization expertise as well as linker-payload synthesis experience. A firm understanding and grasp of chemical biology strategies and the importance of applying both chemical and biological solutions to solve problems in drug discovery will be key. Small molecule synthesis and drug discovery/SAR experience as well as knowledge in the latest and most advanced bioconjugation techniques, platforms, and strategies is desired. </p><p>We expect they will act as an inspiring and motivating leader, effective communicator and manager, and strong collaborator to lead and drive project teams to develop novel antibody-conjugated peptidomimetic therapeutics. The successful candidate will also address challenges related to synthesis, medicinal chemistry, bioconjugation and optimal <em>in vitro</em> and <em>in vivo</em> properties leading to development candidates.</p><p><strong> </strong></p><p><strong>Build our future together: </strong></p><ul><li>Directly supervise and manage the day-to-day activities of the R&D Chemistry Peptidomimetic group, providing vision, inspiration, and both short-term and long-term goals. Communicate priorities, policies, and goals of Regeneron Senior Leaders to the group.</li><li>Perform medicinal chemistry inspired and SAR-driven generation of novel peptidomimetic drug modalities, using synthetically feasible and simplistically designed linkers to provide overall optimal <em>in vitro</em> and <em>in vivo</em> properties of antibody-conjugated therapeutics</li><li>Troubleshoot and optimize peptide potency and stability using standard peptide-based principles (e.g., Ala scans), non-natural amino acid incorporation, alpha-Me/N-Me peptide backbone modifications, and other medicinal chemistry strategies that are guided by <em>in vitro</em> assays, plasma/serum stability, and met ID data.</li><li>Champion and lead the R&D Chemistry Peptidomimetic efforts on internal/external project teams, and demonstrate the ability to multi-task and parallel process to add to our continuous pipeline of Regeneron development candidates</li><li>Identify new strategies and technologies (e.g., linker and payload design) to improve on existing Regeneron platforms for pursuing novel synthesis and bioconjugation of peptidomimetic drug modalities</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic group.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>When & Where:</strong></p><ul><li><h3>This is an on-site position located in our Hawthorne, NY facility</h3></li><li>Occasional travel to our nearby Tarrytown facility may be required</li></ul><p><strong>Discover your role:</strong></p><ul><li>You are passionate and enthusiastic about the promise of peptidomimetic conjugated, antibody-targeted therapeutics and appreciate the challenges and opportunities of drug delivery and molecular targeting.</li><li>You enjoy applying and combining traditional methods and novel technologies to develop solutions for synthesis, bioconjugation and drug discovery.</li><li>You are comfortable working in a cross-functional role and excel as part of a diverse team where egos are checked at the door.</li><li>You want to provide meaningful contributions to the development of an organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li><li>You prefer to work in an organization that is modality agnostic, letting the data determine the best course forward.</li></ul><p><strong> </strong></p><p><strong>In order to be considered qualified for the role, you must have:</strong></p><ul><li>Ph.D. in peptide and/or synthetic organic chemistry or a related field.</li><li>Minimum of 10 years of professional industry experience.</li><li>Extensive drug discovery experience with antibody-targeted peptidomimetic drug modalities, experience with the synthesis and manufacturing of peptidomimetic payloads and linkers, expertise in modern methods in medicinal chemistry structure-activity relationships, and a deep understanding of biological MOAs (extracellular/intracellular target evaluation, ADME/PK, PD/efficacy, toxicological evaluation). </li><li>A track record of success in the field of either peptidomimetics, small molecules or antibody targeted therapeutics (i.e., advancement of molecules into the clinic) with experience building and leading teams is required.<em> </em></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHILADELPHIA SOUTH, PA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48014]]></requisitionid>
    <referencenumber><![CDATA[R48014]]></referencenumber>
    <apijobid><![CDATA[r48014]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48014/medical-account-specialist-ii-neurology-philadelphia-south-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Philadelphia South (Metro), PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -  WHITE PLAINS, NY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48009]]></requisitionid>
    <referencenumber><![CDATA[R48009]]></referencenumber>
    <apijobid><![CDATA[r48009]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48009/medical-account-specialist-ii-neurology-white-plains-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[White Plains]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: White Plains (Metro), NY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Accounting Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47280]]></requisitionid>
    <referencenumber><![CDATA[R47280]]></referencenumber>
    <apijobid><![CDATA[r47280]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47280/manager-accounting-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This role leads Accounting Operations systems and process optimization for biopharmaceutical manufacturing, ensuring a single source of truth across modules, plants, and functions. In addition to core responsibilities, the Manager drives standardization and automation across accounting and ERP workflows. The Manager sets cadence, standards, and systems discipline to deliver accurate, timely, and data-driven outputs that support monthly close, compliance, and operational decision-making.</p><p><strong>A day in the life may look like:</strong></p><ul><li><p>Own end-to-end configuration, maintenance, and governance of accounting’s Oracle applications across OPM, Order Management, Inventory, and Financials</p></li><li><p>Govern close calendars, achievements, templates, and submission protocols to drive accountability and timely, accurate financial results</p></li><li><p>Liaise with Accounting and IT to diagnose and resolve functional setup issues and sophisticated system problems impacting close and financial reporting</p></li><li><p>Engage with process owners to identify automation opportunities, assess feasibility, prioritize implementation, and measure realized efficiency gains</p></li><li><p>Translate business requirements into clear deliverables: functional design specifications, use cases, and workflow/process diagrams</p></li><li><p>Conduct end-to-end testing cycles for application improvements, ERP upgrades, and project implementations, with rigorous impact analysis and UAT sign-off</p></li><li><p>Partner with Manufacturing, Supply Chain, and Corporate Finance to align master data, mappings, and policies across modules for smooth close and reporting</p></li><li><p>Deliver executive-ready outputs: reconciliations, variance analyses, issue logs with root-cause and corrective actions, KPI dashboards, and control health check</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Drive automation of recurring close reporting, reconciliations, exception dashboards, and data quality checks</p></li><li><p>Partner with IT on improvements and UAT</p></li><li><p>Define model structures, hierarchies, and master data standards that enable efficient consolidation, consistent mappings, and flexible scenario analysis.</p></li><li><p>Standardize accounting definitions and cross-module controls for GL, AR, AP, FA, Inventory, and Order Management to reduce manual work and errors</p></li><li><p>Identify and implement improvements that shorten cycle time, strengthen controls, and improve insights for stakeholders across Finance and Operations</p></li><li><p>Translate ambiguous asks into structured solution options with assumptions, risks, effort estimates, and recommendations</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><p>BS/BA in Accounting, Information Systems, or a related field; 7+ years experience</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Mountain West)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48130]]></requisitionid>
    <referencenumber><![CDATA[R48130]]></referencenumber>
    <apijobid><![CDATA[r48130]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48130/field-reimbursement-manager-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong> Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: San Francisco (Metro), CA, Seattle (Metro), WA, Oakland, (Metro), CA, Las Vegas (Metro), NV, Thousand Oaks (Metro), CA Los Angeles (Metro) CA, Riverside (Metro) CA, San Diego, (Metro), CA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[VP Global Procurement - R&D]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48863]]></requisitionid>
    <referencenumber><![CDATA[R48863]]></referencenumber>
    <apijobid><![CDATA[r48863]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48863/vp-global-procurement-rd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>This role can be located in either Tarrytown, NY or Warren, NJ.</strong></p><p>The Vice President, Global Procurement – R&D will provide strategic leadership and direction for the R&D category while operating first and foremost as an enterprise leader who shapes how procurement creates value across Regeneron. This leader will be accountable for establishing category strategies and jointly driving value with business partners across Regeneron's R&D organization, while designing an R&D procurement function that scales with both human capability and technology-driven execution.</p><p>Reporting to the Senior Vice President, Chief Procurement Officer, and working closely with the Global Procurement Leadership Team and executive stakeholders in R&D, this leader will define sourcing, clinical research organization, clinical services, and lab supplies strategies while modernizing the processes, technology, and talent model that deliver them. They will prioritize the interests of Regeneron, its patients, shareholders, and people in every decision — translating supplier relationships, supply chain resilience, and sustainability into tangible, long-term competitive advantage.</p><p><strong>In This Role, You Will</strong></p><ul><li>Act as an influential enterprise leader across senior stakeholders, leveraging critical thinking, change management, strong business acumen, and deep procurement expertise to develop strategic improvements that extend well beyond the R&D category.</li><li>Lead and/or participate in senior management discussions related to the R&D category, setting priorities aligned with stakeholder needs and representing Global Procurement in decisions with critical short- and long-term impact on the company.</li><li>Design and lead an R&D procurement function that scales with both human capability and technology-driven execution — re-engineering processes and embedding automation and intelligent tooling to free the team for higher-value work.</li><li>Champion the adoption and optimization of technology platforms that drive process automation, data-driven decision-making, and end-to-end visibility across the procurement lifecycle, acting as a change leader who builds buy-in and sustains adoption.</li><li>Lead critical negotiations, supplier management, and stakeholder engagement for the R&D category, turning supplier relationships into a true competitive differentiator through partnership and innovation.</li><li>Build risk and supply chain resilience into category and sourcing strategies, anticipating disruption and ensuring continuity of supply for the suppliers, services, and materials most critical to R&D.</li><li>Build agile, value-driving talent that keeps pace with business demands, taking accountability for development, retention, and recruiting of Global Procurement talent.</li><li>Apply in-depth knowledge of efficient global procurement organizations within the biopharmaceutical industry, using Regeneron's global capability center to standardize repeatable activities and optimize efficiency.</li><li>Exhibit role-model leadership behaviors across the organization, communicating a clear and compelling vision and driving positive change with senior executives and Regeneron's most critical suppliers.</li><li></li></ul><p><strong>This Role Might Be For You If You Have</strong></p><ul><li>A bachelor's degree in a relevant field (required); an advanced degree (MBA or similar) and/or a professional procurement certification is strongly preferred.</li><li>~20 years of progressive experience in global procurement or category management, including a track record of taking on broader scope, higher-stakes categories, and larger teams at each career step — not just tenure, but demonstrated upward trajectory.</li><li>Direct experience leading procurement within a multi-national biopharmaceutical or life sciences organization, with working fluency in the R&D category specifically — sourcing, CRO/clinical services, and lab supplies — or in closely adjacent, comparably complex categories.</li><li>A demonstrated record of enterprise-level influence: examples of shaping decisions or strategy beyond procurement's own four walls, gained credibility with C-suite or senior R&D executives, and led change that stuck rather than stalled after rollout.</li><li>Hands-on ownership of building or substantially re-engineering a procurement function — not just using existing tools, but having redesigned processes, embedded automation or intelligent tooling, and measurably shifted team capacity toward higher-value work.</li><li>Command of complex, high-value negotiations and supplier relationships, with specific, quantifiable outcomes (cost savings, risk mitigated, capacity secured, innovation unlocked) rather than general negotiation experience.</li><li>Evidence of building supply chain resilience proactively — anticipated and managed a real disruption or continuity risk for a critical category, rather than only responding after the fact.</li><li>Direct people-leadership experience managing Director-level (or equivalent senior) professionals, including specific examples of developing successors and retaining high performers through organizational change.</li></ul></div><ul></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - LEXINGTON, KY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48021]]></requisitionid>
    <referencenumber><![CDATA[R48021]]></referencenumber>
    <apijobid><![CDATA[r48021]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48021/medical-account-specialist-ii-neurology-lexington-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Lexington-Fayette]]></city>
    <state><![CDATA[Kentucky]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Lexington (Metro), KY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Bethesda, MD]]></title>
    <date><![CDATA[Thu, 09 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48431]]></requisitionid>
    <referencenumber><![CDATA[R48431]]></referencenumber>
    <apijobid><![CDATA[r48431]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48431/medical-specialist-i-pulmonology-bethesda-md/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Maryland]]></city>
    <state><![CDATA[Maryland]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Bethesda, MD - representative must reside within the territory.</strong></p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups.</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p>​<strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, External Manufacturing]]></title>
    <date><![CDATA[Wed, 15 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49012]]></requisitionid>
    <referencenumber><![CDATA[R49012]]></referencenumber>
    <apijobid><![CDATA[r49012]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49012/senior-manager-external-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, External Manufacturing (Operations Lead) to drive day-to-day execution, operational readiness, and world-class performance across our Contract Manufacturing Organization (CMO) network while leading a team focused on continuous improvement and technical excellence.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li><li><p>Travel requirement: 25-50%</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Ensures product manufacture occurs in compliance with cGMP and applicable regulations.</p></li><li><p>Facilitates all External Manufacturing activities at CMO/partner sites: batch scheduling, supply of materials, direct shipment, cycle time tracking, reports and technical expertise.</p></li><li><p>Ensures, in collaboration with EM Project Management, timely routing/review of technical transfer activities, validation plans, MRs, SOPs, and other documentation.</p></li><li><p>Implements site initiatives in production operation as directed by site management.</p></li><li><p>Leads continuous improvements, system implementations and/or strategy development to reduce cycle times and improve efficiency for area.</p></li><li><p>Ensures off-site inspections, testing and shipping/packaging is done according to guidelines and specifications.</p></li><li><p>Ensures product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers.</p></li><li><p>Supports investigations which concern External Manufacturing or associated shipping operations, as required.</p></li><li><p>Manages direct reports and/or lead a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.</p></li><li><p>Assists in developing metrics to analyze department activities, workload and performance.</p></li><li><p>Maintains required training status on Regeneron specific work instructions and SOPs.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in business or scientific discipline and 8 years of related experience, including a minimum of 5 years of direct cGMP manufacturing operations experience (clinical and/or commercial); remaining years may be satisfied through supplier management experience or equivalent combination of education and experience. MBA preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, New Products]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49405]]></requisitionid>
    <referencenumber><![CDATA[R49405]]></referencenumber>
    <apijobid><![CDATA[r49405]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49405/director-new-products/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, New Products and Commercial Development leads commercial strategy and value maximization for key pipeline assets within Regeneron's portfolio. Partnering closely with Clinical Development and other key functions, the role shapes strategic vision, informs development decisions, and advances early launch planning for high-priority programs spanning various stages of development.</p><h3>When & where:</h3><ul><li>Sleepy Hollow, NY for 4 days a week in office</li></ul><h3>Discover your role:</h3><ul><li>Provide commercial leadership to shape the strategic vision, program strategy, value proposition, and development plan of early and pre-launch development programs</li><li>Communicate a clear, well-reasoned commercial perspective to development leadership as a core member of cross-functional Strategic Program Teams</li><li>Lead key commercial deliverables as needed for each stage of development, including target product profile (TPP) development, positioning/key claims, brand naming, launch readiness and lifecycle optimization</li><li>Collaborate with marketing research, analytics, strategic analysis and competitive intelligence to develop strategic insights and ensure fact-based decision making and forecasting</li><li>Contribute commercial insights to program related decision points on device, formulation, dosing frequency, packaging, distribution channel and other critical product attributes</li><li>Provide commercial input to clinical trial design, endpoint selection and prioritization, to ensure programs may deliver competitive claims</li><li>Partner with Market Access and HEOR teams to build differentiated value propositions and indications prioritizations to support optimal access in US and International markets</li><li>Develop commercialization plans in partnership with key functions, including Marketing, Access, Insights, Medical, Communications, Legal, Regulatory, and Sales</li><li>Present to commercial and development leadership as needed</li><li>Support business development activities in aligned therapeutic areas, including diligence and commercial case development</li></ul><h3>This role requires:</h3><ul><li>12+ years of pharmaceutical or biotech industry experience, including at least 10 years of pharmaceutical marketing and/or related commercial experience</li><li>Experience in new product commercialization and/or launching new pharmaceutical or biotech products is strongly preferred</li><li>Strong scientific acumen with knowledge of immunology/inflammation and/or obesity disease areas</li><li>Working knowledge of the legal and regulatory environment governing pharmaceutical and biotech commercialization</li><li>Background in industry-relevant consulting, investment analysis, health economics and outcomes research, or related fields is a plus</li><li>Proven ability to lead and influence cross-functionally, building strong relationships across internal teams, alliance partners, and health care providers, with strong learning agility</li><li>Ability to combine strategic thinking with business and scientific acumen, translating complex data and clinical information into clear, actionable recommendations</li><li>Ability to thrive in a fast-paced, ambiguous environment, independently managing multiple projects against tight deadlines</li><li>Need to be entrepreneurial and innovative, with strong written and verbal communication skills</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology (TN, AL, MS, AR)]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46458]]></requisitionid>
    <referencenumber><![CDATA[R46458]]></referencenumber>
    <apijobid><![CDATA[r46458]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46458/associate-director-field-medical-affairs-hematology-tn-al-ms-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Territory: Tennessee, Alabama, Mississippi and Arkansas (residency in the territory is required with a preference of TN and AL</p><p>Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p><br><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. </p><p><br>#medicalscienceliaison #msl #HFM</p><p>#msl #medicalscienceliaison #HFM #AD<br> </p><p><strong> </strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Corporate Counsel - Privacy/ Transactions]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47353]]></requisitionid>
    <referencenumber><![CDATA[R47353]]></referencenumber>
    <apijobid><![CDATA[r47353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47353/senior-director-corporate-counsel-privacy-transactions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build Our Future Together</strong></p><p>Regeneron Pharmaceuticals is seeking a highly experienced transactions attorney for a pivotal role to serve as a transactional attorney and liaison to the Regeneron Data Privacy Office. This position will act as a privacy expert within the Transactions & Contracts team offering guidance to colleagues on privacy law and ensuring that privacy provisions are seamlessly integrated into our contracts. The position also involves drafting, reviewing, negotiating, and providing strategic counsel on a diverse portfolio of significant agreements across our innovative business units, overseeing the operations of Regeneron’s contract lifecycle management system, including managing the group’s Associate Director, Contracts and Systems Operations.</p></div><div><div><div><div><div><div><div><div><div><p>Your expertise will be instrumental in advising the Transactions Team on complex privacy issues, requiring a deep understanding of life sciences, business transactions, and data privacy. We are looking for a candidate with exceptional drafting and negotiation skills, life sciences law expertise, leadership capabilities and a proven track record of progressive experience in contract law and data privacy. The ideal candidate thrives in collaborative settings, working alongside multiple stakeholders to provide comprehensive legal solutions that drive Regeneron's success.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Cambridge, MA</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing legal support for a particular area of business transactions, which may include research collaboration agreements, master services agreements, consulting services agreements, license agreements, data use agreements, laboratory services agreements and confidentiality agreements, among others.</p></li><li><p>Maintaining subject matter expertise in data privacy laws and the Regeneron privacy policies and advising Transaction Law colleagues and clients on developments of importance.</p></li><li><p>Providing ongoing one-on-one support to members of the Transaction Law team and coordinating with internal teams and external resources to negotiate and finalize data privacy language in third-party agreements.</p></li><li><p>Responding to U.S. and ex-U.S. contracting questions.</p></li><li><p>Managing updates to the group’s data privacy contracting playbook.</p></li><li><p>Creating data privacy contracting tools and training materials.</p></li><li><p>Managing office hours with internal business partners.</p></li><li><p>Developing and training on privacy contracting tools and requirements.</p></li><li><p>Acting as liaison for the Transactions Law Group with the Data Privacy Office on data privacy policy questions and approaches.</p></li><li><p>Providing strategic direction and oversight for Regeneron’s contract lifecycle management system, including serving as the manager of the team’s Associate Director, Contracts Systems and Operations.</p></li><li><p>Providing contract law support for the Regeneron Cell Medicines team in Cambridge.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>JD with excellent law school credentials.</p></li><li><p>Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel is preferred.</p></li><li><p>At least 15 years of legal experience at a law firm and/or in-house, with biotech/pharmaceutical and/or health care experience. </p></li><li><p>Solid understanding of contracts and related law. Experience with contracts involving data privacy and intellectual property. </p></li><li><p>Experience in strategic leadership of contract management systems or similar role is preferred. </p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QC Technical Resources Specialist (Associate - Senior)]]></title>
    <date><![CDATA[Wed, 15 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49155]]></requisitionid>
    <referencenumber><![CDATA[R49155]]></referencenumber>
    <apijobid><![CDATA[r49155]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49155/qc-technical-resources-specialist-associate-senior/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> QC Technical Resources Specialist</strong> to join our <strong>QC Technical Resources </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Supporting assay development/validation activities for the QC group from method readiness through to validation.</li><li>Ensuring the operational readiness through management of sample / material requests.</li><li>Coordinating analytical assay transfer internally and externally.</li><li>Reviewing analytical development reports, assay and process validation reports and other technical documents for technical correctness and regulatory compliance.</li><li>Communication of method updates to partners and tracks progress of updates.</li><li>Coordinating multi-site trending and reviews and communicates information as needed to subject matter experts.</li><li>Supporting method Lifecycle activities including method performance reporting, quality metrics and project timelines.</li><li>Tracking team activities and timelines to ensure that the deliverables within the project plans are met and are on-time.</li><li>Communication to management for validation/transfer timelines.</li><li>Continuously driving to improve processes for improved performance.</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Strong ability to work independently and part of a global team.</li><li>Proficient with the Microsoft suite and project management tools.</li><li>Effective time management.</li><li>Excellent written and verbal communication skills.</li><li>Ability to develop strategies and metrics to measure effectiveness.</li><li>Identifying and effectively communicating risks.</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><strong>Associate Specialist: </strong>Requires BS/BA in a life sciences (or related) field and 0-2 years experience or equivalent combination of education and experience.</li><li><strong>Specialist: </strong>Requires BS/BA in a life sciences (or related) field and at least 2 years of relevant experience in a cGMP environment or equivalent combination of education and experience.</li><li><strong>Senior Specialist:</strong> Requires BS/BA/MSc in a life sciences (or related) field and 4-5 years of relevant experience in a cGMP environment or equivalent combination of education and experience.</li></ul><h3>Thrive today. Grow tomorrow.</h3><h3>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQC</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst - Research Program Management]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48912]]></requisitionid>
    <referencenumber><![CDATA[R48912]]></referencenumber>
    <apijobid><![CDATA[r48912]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48912/principal-business-analyst-research-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Principal Business Analyst Research Program Management (RPM), will work collaboratively with Research Program Managers, Research & Preclinical Development scientists, as well as other IT stakeholders, to understand and document scientific drug discovery and data processes and translate these into requirements for the development of data and technology solutions that support Regeneron’s scientific mission. </p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Translate business strategies, goals, and objectives into clear requirements; document problem statements with quantifiable business value </p></li></ul><ul><li><p>Document “as is” and “to be” business processes; identify, verify, and document functional and non-functional requirements using standard methodologies and tools </p></li></ul><ul><li><p>Map information system connections and data flows between systems; identify data elements and provide data mapping and data dictionaries </p></li></ul><ul><li><p>Write SQL statements to investigate data; understand data lake principles and different database types </p></li></ul><ul><li><p>Maintain and prioritize the backlog of requests; ensure the development team has absolute clarity on requirements; manage business stakeholder expectations </p></li></ul><ul><li><p>Work with scientists and laboratory personnel to understand business processes and suggest improvements; partner with research scientists and technical teams to define system goals and requirements </p></li></ul><ul><li><p>Pursue data quality issues to root cause; collaborate with business and IT partners to address issues intelligently </p></li></ul><ul><li><p>Handle a variety of tasks, effectively solve problems with complex variables, and shift priorities as needed in a fast-paced research environment </p></li></ul><ul><li><p>Work alongside stakeholders to test solutions for accuracy and consistency of results.</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Master’s degree in a life science with experience in computer science or information technology.</p></li><li><p>7+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment. </p></li><li><p>Previous experience in the biotechnology and/or pharmaceutical industry is required. We need someone who is adept at using a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, data and process modeling frameworks) in order to perform business analysis, elicit and document requirements, map data flows, and drive data quality improvements in a research-focused environment.</p></li><li><p>Previous experience with drug discovery program management, biological laboratory techniques, bioinformatics methods, relational database concepts, IT project and software development lifecycle methodologies, and managing or leading software development projects is preferred. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Information Technology Program Manager]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48901]]></requisitionid>
    <referencenumber><![CDATA[R48901]]></referencenumber>
    <apijobid><![CDATA[r48901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48901/information-technology-program-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The IT Program Manager VI-Train will work collaboratively with business stakeholders in multiple scientific areas involved in our Biologics Therapeutic Discovery Pipeline to perform robust project and portfolio planning, and then execute upon that plan to completion; aligning to the project management triple constraint of scope, time and cost. We see this position as critical to executing IT projects for Regeneron and specifically, the VI-Train. The candidate must have excellent time management skills to function in a fast-paced environment, demonstrating independent work skills, strong work ethic, and a passion for helping to fuel the Research IT pipeline. The candidate will be responsible for coordinating project activities from ideation through transition to the run team. The ideal candidate will have notable experience in planning, monitoring and closing projects, and coordinating multiple workstreams. We hope you are excited by this opportunity to transform Regeneron’s approach to IT project management and execution. </p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Responsible for activities of a highly complex nature, which may include small projects or large programs involving multiple project workstreams, and act as a single point of contact for those activities </p></li></ul><ul><li><p>Actively manage large projects directly with varying degrees of complexity, and coordinate multiple project streams with inter-dependencies </p></li></ul><ul><li><p>Utilizing agile methodologies such as Scaled Agile Framework (SAFe) </p></li></ul><ul><li><p>Recommend and take action to direct the analysis and solution of problems </p></li></ul><ul><li><p>Communicate with stakeholders on an ongoing basis; estimate resources and participants needed to achieve project goals; draft and submit budget proposals and recommend subsequent budget changes where necessary; manage multiple projects as necessary </p></li></ul><ul><li><p>Plan and schedule project timelines and milestones using appropriate tools; track project milestones and deliverables; develop and deliver progress reports, proposals, requirements documentation and presentations </p></li></ul><ul><li><p>Acting as the go-to-person and single point of contact for status and plans involving complex and inter-dependent program </p></li></ul><ul><li><p>Coordinate with IT and department managers to assess and track plans, status, etc. for on-time delivery of critical projects and programs; this includes assisting teams and the project teams in removing impediments and resolving cross-team issues </p></li></ul><ul><li><p>Ability to define the project objectives clearly and rally a team around the value delivery plan </p></li></ul><ul><li><p>Ensure teams keep a laser focus on what needs to be completed, and when, to keep programs on track </p></li></ul><ul><li><p>Looking ahead anticipating risks before they are issues </p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Master’s degree in a life science with experience in computer science or information technology.</p></li><li><p>7+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment. </p></li><li><p>Someone adept at using a variety of technologies (Planview, Jira, MS tools, etc.) and processes (SDLC, PMO, etc.) Previous project management in a Research organization is preferred. Must be open to travel periodically (~5%) to represent Regeneron as needed and for internal meetings. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Dir Product Management]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49123]]></requisitionid>
    <referencenumber><![CDATA[R49123]]></referencenumber>
    <apijobid><![CDATA[r49123]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49123/assoc-dir-product-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Job Description</div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p></div></div></div></div></div></div></div></div></div><p>The Global Development IT (GD IT) Associate Director, Product Lead is a leader within the GD IT Delivery & Operations organization, accountable for the strategy, delivery, and continuous improvement of a portfolio of technology products spanning standards-led protocol digitization (USDM/ICH M11), Digital Data Flow (DDF), and human sample lifecycle management. This role may provide line management to a team of Product Leads and Product Analysts, set the domain vision and roadmap, and partner with senior business stakeholders, Business Solution Partners (BSPs), Business Process Owners, SMEs, Corporate IT, and vendor partners to translate enterprise priorities into capabilities that enable standard-led protocol digitization, biospecimen and sample management, and AI/agentic orchestration across Global Development. The Associate Director assumes domain-level product ownership, including end-to-end implementation, governance, compliance, and support for all products that fall within the domain.</p><p><strong>Where: </strong>Based at our Warren, NJ location</p><p><strong>When: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li>Lead, coach, and develop a team of Product Leads and Product Analysts across protocol digitization, biospecimen/sample management, and AI/agentic orchestration</li><li>Set objectives, build domain capabilities, and instill a process-improvement culture.</li></ul><ul><li>Own the multi-product domain strategy, vision, and roadmap for standards-led protocol digitization (USDM/ICH M11), Digital Data Flow (DDF), and the human sample lifecycle, prioritizing and making trade-offs across product lines.</li><li>Build and manage senior stakeholder relationships across BSPs, Business Process Owners, SMEs, Corporate IT, and vendors</li><li>Chair domain steering committees and governance forums and drive alignment, consistency, and reuse across Product Leads</li><li>Take end-to-end ownership of the domain product portfolio—implementation, performance, and continuous improvement—overseeing requirements, testing/UAT, risk-based CSV, and ITIL-aligned release, change, and incident processes to meet business expectations, audit readiness, and compliance</li><li>Intake, assess, prioritize, and validate domain requirements in partnership with BSPs, managing scope, dependencies, and trade-offs to align technology roadmaps with product priorities.</li><li>Set direction for human-in-the-loop, multi-agent orchestration and regulated-AI governance (prompt/version control, evaluation, audit trails, risk-based CSV) aligned to 21 CFR Part 11/Annex 11 and GxP.</li><li>Drive build-vs-buy assessments, RFPs, software/services contracting, and vendor performance management; identify resourcing needs and oversee internal, vendor, and managed-service delivery.</li><li>Direct establishment of the digital protocol and structured Schedule of Activities as system of record, ensuring traceable continuity from protocol intent through CRF/EDC to SDTM, ADaM, and analysis outputs.</li><li>Provide direction over biospecimen/sample standards, metadata, and the integration ecosystem (MDR, EDC, IRT, LIMS/LIS, CTMS, analytics), ensuring lineage and reconciliation aligned to central and specialty lab operating models.</li><li>Provide subject matter expertise to manage business expectations, timelines, and domain budget; present innovative solutions and represent the organization in industry and standards forums (e.g., TransCelerate DDF, CDISC 360).</li><li>Collaborate with GD IT, Corporate IT, and other functions on enterprise systems, standards, and governance, serving as senior point of contact and escalation for the domain across Global Development.</li></ul><p><strong>This role requires: </strong></p><ul><li>Strong command of ICH M11/USDM, CDISC SDTM/ADaM, controlled terminology, and standards governance, with demonstrated delivery of structured protocol authoring and protocol-to-data automations with traceable lineage into SDTM/ADaM; experience with USDM-aligned tools (e.g., Nurocor) or equivalent MDRs</li><li>Excellent communication skills and the ability to influence senior leaders and stakeholders, including executive-ready communications</li><li>Practical understanding of human sample workflows in clinical trials (kit management, barcoding, collection/processing, shipping/receipt, chain of custody, reconciliation), central/specialty lab operating models, and biospecimen/lab and SAP/EDC integrations</li><li>Experience managing technology capability identification, selection, implementation, and operations, including LIMS/LIS integrations with EDC, IRT, CTMS, and analytics, and vendor governance across global teams</li><li>Experience applying AI and multi-agent/agentic systems (tool/function calling, RAG, prompt management, evaluation, monitoring) with human-in-the-loop controls, plus technical fluency in integration patterns (REST/GraphQL APIs, events) and data pipelines (ETL/ELT) on modern cloud platforms</li><li>Knowledge of pharmaceutical Global Development business capabilities, processes, and systems and of SDLC and ITSM/ITIL frameworks, with strong project, budget, and stakeholder management skills and demonstrated success interacting with senior leadership</li><li>Preferred: familiarity with SQL/Python or R for prototyping/validation and MLOps in regulated environments (model/package registries, approval workflows); exposure to TransCelerate DDF and CDISC 360 initiatives</li><li>Experience applying risk-based CSV and regulated-AI governance (audit trails, evaluation, prompt/version control) aligned to 21 CFR Part 11/Annex 11, GxP, and data protection (HIPAA/GDPR, RBAC)</li><li>Experience hiring, supervising, motivating, and coaching a team of direct reports—including leading or mentoring Product Leads/Product Managers—instilling a process-improvement culture and championing agile ways of working across cross-functional partners</li><li>Experience leading an end-to-end product launch or shutdown across multiple teams.</li></ul><ul><li>Ability to act tactically and think strategically, switching leadership styles to influence, guide, and coach, and to manage multiple priorities and a portfolio of products amid ambiguity and changing priorities</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Northeast]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48149]]></requisitionid>
    <referencenumber><![CDATA[R48149]]></referencenumber>
    <apijobid><![CDATA[r48149]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48149/neurology-account-director-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Massachusetts]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Northeast (New York, Pennsylvania, Massachusetts, Vermont, New Hampshire, Maine)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47182]]></requisitionid>
    <referencenumber><![CDATA[R47182]]></referencenumber>
    <apijobid><![CDATA[r47182]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47182/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, QA Validation & Computer Systems Assurance]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48630]]></requisitionid>
    <referencenumber><![CDATA[R48630]]></referencenumber>
    <apijobid><![CDATA[r48630]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48630/director-qa-validation-computer-systems-assurance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Saratoga Springs]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of QA Validation to lead the QA Validation, Computer Systems Assurance (CSA), and Equipment Assurance functions for the Regeneron manufacturing site located in Saratoga Springs, NY. The director is responsible for qualification and validation strategy across a highly automated, digitally integrated biopharmaceutical facility, including process equipment, utilities, manufacturing execution systems (MES), laboratory information management systems (LIMS), distributed control systems (DCS), and enterprise platforms. The role applies risk-based methodologies aligned with FDA CSA guidance, GAMP 5 (2nd ed.), ICH Q9(R1)/Q10, and SDLC frameworks to maintain validated state across commercial and clinical manufacturing, and represents and defends the validation and CSA programs during FDA, EMA, and other regulatory inspections.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Saratoga Springs, NY and Rensselaer, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Own and maintain the site Validation Master Plan (VMP), including scope for process, cleaning, sterilization, utilities, and equipment qualification across GMP manufacturing areas</p></li><li><p>Design and implement risk-based qualification and requalification programs consistent with current FDA, EMA, and ICH guidance</p></li><li><p>Ensure validation lifecycle documentation (URS, DQ, IQ, OQ, PQ, PV) meets regulatory expectations for commercial and clinical programs</p></li><li><p>Lead periodic review programs to maintain validated state for equipment, utilities, and automated systems</p></li><li><p>Lead the CSA program in alignment with FDA's 2022 CSA guidance and GAMP 5 (2nd ed.), shifting from prescriptive CSV toward risk-based, fit-for-purpose assurance activities</p></li><li><p>Own the site SDLC framework governing qualification and assurance of GxP-relevant software and computerized systems, including MES (e.g., Syncade, PAS-X), DCS/SCADA, LIMS, EBR, ERP integrations, and data historians</p></li><li><p>Establish critical thinking and scripted/unscripted testing strategies based on software category, intended use, and risk to product quality and patient safety</p></li><li><p>Oversee supplier/vendor assessments for software used in GxP contexts, including software development lifecycle practices and audit readiness</p></li><li><p>Ensure data integrity by design across automated and integrated systems, including audit trail configuration, access controls, and electronic records compliance (21 CFR Part 11/Annex 11)</p></li><li><p>Partner with IT, automation, and manufacturing engineering teams to integrate CSA requirements into system procurement, development, and change management processes</p></li><li><p>Provide QA oversight for qualification of highly automated systems, including continuous manufacturing platforms, inline/online/atline PAT instruments, and automated material handling systems</p></li><li><p>Partner with automation and digital transformation teams to ensure GxP requirements are embedded in future-state manufacturing architecture, including digital twin environments</p></li><li><p>Review and approve GxP documents including validation protocols and reports, CSA plans and assessments, change controls, deviations/failure investigations, risk assessments, SOPs, and the VMP</p></li><li><p>Provide QA validation and CSA oversight within the site change control system, ensuring impact assessments and requalification/revalidation requirements are properly scoped</p></li><li><p>Maintain periodic review programs for validated processes and qualified systems, including metrics-driven risk prioritization</p></li><li><p>Present and defends validation and CSA programs during FDA, EMA, and other regulatory agency inspections; leads preparation of inspection-ready documentation and staff readiness</p></li><li><p>Monitor evolving regulatory guidance (FDA, EMA, PIC/S, USP) relevant to validation, CSA, data integrity, and computerized systems</p></li><li><p>Lead, develop, and retain a team of validation scientists, engineers, and CSA specialists across a complex, multi-system GMP environment</p></li><li><p>Develop and manage validation and CSA budgets, contractor resources, and schedules; sets performance objectives and manages hiring and separation activities</p></li><li><p>Collaborate with Manufacturing, Engineering, Automation, IT, and Regulatory Affairs to align validation and CSA strategies with site priorities and enterprise digital initiatives; communicates program status and risk posture to senior leadership</p></li><li><p>Support global quality alignment across Regeneron manufacturing facilities on validation and CSA standards and best practices</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA required in Engineering, Computer Science, Life Sciences, or related field; advanced degree preferred</p></li><li><p>12+ years of experience in pharmaceutical or biopharmaceutical manufacturing, including at least 7 years in validation, CSA, or quality assurance roles</p></li><li><p>5+ years of people management experience in a GxP environment</p></li><li><p>Direct experience leading computer systems assurance or CSV programs for commercial biologics or pharmaceutical manufacturing sites required</p></li><li><p>Working knowledge of SDLC methodologies applied to GxP software (GAMP 5, 2nd ed.), FDA CSA guidance (2022), 21 CFR Part 11, EU Annex 11, and ICH Q9(R1)/Q10</p></li><li><p>Experience with MES, DCS/SCADA, LIMS, and ERP/EBR systems in a GMP context required</p></li><li><p>Experience representing validation and CSA programs in regulatory inspections (FDA PAI, BPAI, or EMA inspections) preferred</p></li><li><p>Strong working knowledge of risk management principles and their application to validation and software assurance decisions</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II  - HEMATOLOGY - RICHMOND, VA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47832]]></requisitionid>
    <referencenumber><![CDATA[R47832]]></referencenumber>
    <apijobid><![CDATA[r47832]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47832/medical-account-specialist-ii-hematology-richmond-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Richmond]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Richmond, VA, Norfolk, VA, Virginia Beach, VA, Charleston, WV, Morgantown, WV</strong></p><p>The Hematology Oncology Account Specialist, is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Hematology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of two bispecific agents to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - MEMPHIS, TN]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48923]]></requisitionid>
    <referencenumber><![CDATA[R48923]]></referencenumber>
    <apijobid><![CDATA[r48923]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48923/medical-account-specialist-ii-hematology-memphis-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: <strong>Memphis, Jackson, MS, Jonesboro, AR</strong></p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II NEUROLOGY- LOUISVILLE, KY]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48053]]></requisitionid>
    <referencenumber><![CDATA[R48053]]></referencenumber>
    <apijobid><![CDATA[r48053]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48053/medical-account-specialist-ii-neurology-louisville-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Louisville-Jefferson County5]]></city>
    <state><![CDATA[Kentucky]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Louisville (Metro), Kentucky </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (South Central)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48129]]></requisitionid>
    <referencenumber><![CDATA[R48129]]></referencenumber>
    <apijobid><![CDATA[r48129]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48129/field-reimbursement-manager-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Dallas/Houston, (Metro) TX</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Diagnostics CDx (Precision Medicine)]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48167]]></requisitionid>
    <referencenumber><![CDATA[R48167]]></referencenumber>
    <apijobid><![CDATA[r48167]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48167/senior-manager-clinical-diagnostics-cdx-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Diagnostics to support end-to-end companion diagnostics (CDx) strategy and execution across our therapeutic indications. In this role, you will translate scientific needs into fit-for-purpose assays for global decisions, owning programs from feasibility through validation, registration, launch, and post-market sustainment, while partnering with biomarker, clinical, regulatory, commercial, and IVD collaborators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li><li><p>Travel percentage: Up to 5-10% for partner meetings, clinical site visits, and regulatory interactions.</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Execute end-to-end CDx strategy, aligning diagnostic milestones with therapeutic clinical development and regulatory timelines</p></li><li><p>Lead cross-functional teams, integrate workstreams, clear obstacles, and provide transparent status reporting to governance bodies and senior leadership</p></li><li><p>Manage IVD partners, negotiating scope, timelines, budgets, and quality, and overseeing co-development and Joint Steering Committees</p></li><li><p>Define assay intent and contribute to target product profiles for CDx platforms (e.g., NGS, PCR, IHC, Immunoassays), driving analytical and clinical validation</p></li><li><p>Embed CDx assays in trials with clinical teams, covering screening/stratification, sampling, site readiness, and lab operations</p></li><li><p>Partner with IVD Regulatory on global submissions (FDA, EU IVDR, PMDA), supporting pre-subs, labeling, and responses</p></li><li><p>Ensure compliance with quality and regulatory frameworks (ISO 13485/14971, CLSI, IVDR, GCP), maintaining documentation and audit readiness</p></li><li><p>Thrive in a fast-paced, multi-tasking environment, bringing strong communication skills to cross-functional collaboration.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced degree in molecular biology, pathology, biomedical engineering, or equivalent experience</p></li><li><p>4+ years in diagnostics development, including 2+ years leading CDx/IVD programs in pharma or diagnostics organizations</p></li><li><p>Proven delivery of CDx aligned to drug approvals, with successful validation and regulatory submissions</p></li><li><p>Expertise in NGS, PCR, IHC, and immunoassays, along with validation standards and quality systems</p></li><li><p>Strong grasp of global regulatory pathways (FDA CDRH, EU IVDR, PMDA) for CDx labeling</p></li><li><p>Excellent communication, leadership, and stakeholder management skills, with the ability to deliver clear updates to executive audiences</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, Neuroscience]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48792]]></requisitionid>
    <referencenumber><![CDATA[R48792]]></referencenumber>
    <apijobid><![CDATA[r48792]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48792/sr-associate-scientist-neuroscience/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Associate Scientist to join our Neurotherapeutics research team, supporting R&D efforts to generate novel therapeutics for neurodegenerative diseases, including Alzheimer's Disease. In this role, you will conduct lab experiments and research studies that validate therapeutic targets and advance technologies for delivering therapeutics to the central nervous system, while collaborating closely with your research team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Conduct lab experiments and research studies to validate therapeutic targets for neurodegenerative diseases</p></li><li><p>Establish new models of neurodegenerative diseases to support target discovery</p></li><li><p>Screen preclinical therapeutic candidates to advance promising programs</p></li><li><p>Advance technologies that more effectively deliver therapeutics to the central nervous system</p></li><li><p>Perform in vivo experiments, including stereotaxic surgeries, brain injections, systemic injections, mouse handling, and blood/tissue collection</p></li><li><p>Run biochemical and immunoassays such as immunohistochemistry, immunofluorescence, Western blotting, and ELISAs</p></li><li><p>Analyze data using software such as HALO, PRISM, and Excel</p></li><li><p>Thrive in a fast-paced environment, staying detail-oriented and organized while managing multiple tasks</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS with 3-6 years of laboratory research experience, or MS with 2-5 years</p></li><li><p>Experience with in vivo experiments, including stereotaxic surgeries, brain injections, systemic injections, mouse handling, and blood/tissue collection</p></li><li><p>Experience with biochemical and immunoassays (e.g., immunohistochemistry, immunofluorescence, Western blotting, ELISAs, tissue lysis and processing)</p></li><li><p>Experience with data analysis software, including HALO, PRISM, and Excel</p></li><li><p>Strong communication and organizational skills, with the ability to work well in a team</p></li><li><p>Preferred: knowledge of Alzheimer's biology and a genuine passion for scientific research</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations, GMP IT/OT]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43879]]></requisitionid>
    <referencenumber><![CDATA[R43879]]></referencenumber>
    <apijobid><![CDATA[r43879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43879/associate-director-of-it-operations-gmp-itot/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Operations Leader (Senior Manager or Associate Director) to join our IOPS IT team, ensuring the reliable operation and management of IT and Operational Technology infrastructure and services across our GxP manufacturing environment. In this role, you will provide strategic direction and operational oversight for IT/OT infrastructure, service delivery, and compliance — while collaborating with corporate IT, automation teams, service providers, and cross-functional partners to maintain robust, secure, and scalable operations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Ensure reliable operation of IT/OT infrastructure including servers, hardware, communications, desktop support, and wireless networks; provide operational oversight for data centre operations, network services, telecom, and asset management</li><li>Define, implement, and lead IT/OT infrastructure architecture with a focus on hyper-converged systems, advanced networking, and wireless technologies to ensure robust connectivity and security across industrial and enterprise environments</li><li>Maintain compliance with GxP, FDA, and global regulatory requirements; ensure data integrity, disaster recovery planning, and robust security measures are in place across IT/OT infrastructure</li><li>Maintain compliance with automation system standards including DeltaV/Emerson and Rockwell/Allen-Bradley; ensure systems and procedures support effective monitoring and reporting</li><li>Manage service providers to ensure high-quality delivery aligned to SLAs; act as escalation point for major incidents and provide regular management reporting on service performance and IT operations</li><li>Collaborate with corporate IT and OT partners to ensure seamless system integration and alignment across the enterprise</li><li>Lead, mentor, and develop a diverse technical team spanning Helpdesk, Desktop, Server, and Network functions; oversee recruitment, training, performance evaluations, and goal setting for the IT Operations team</li><li>Drive implementation and continuous improvement of ITIL practices, SLAs, metrics, and operational best practices across the IT Operations function</li><li>Demonstrated experience managing diverse technical teams including Helpdesk, Desktop, Server, and Network staff; experience managing vendors and managed service providers required</li><li>Experience developing and deploying SLAs, metrics, and operational best practices; proven track record implementing ITIL practices within an organization</li><li>Strong background in Microsoft OS including Server and GPO elements; strong understanding of data integrity and associated tools</li><li>Experience with Business Continuity and Disaster Recovery planning required</li><li>Knowledge of IT compliance guidelines including PIC/S, 21 CFR Part 11, Annex 11, and GAMP preferred</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology or a related field</li><li>Senior Manager: 8+ years of progressively more responsible experience, including 8+ years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment</li><li>Associate Director: 10 years of progressively more responsible experience, including 10 years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Hematology Oncology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48752]]></requisitionid>
    <referencenumber><![CDATA[R48752]]></referencenumber>
    <apijobid><![CDATA[r48752]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48752/senior-medical-director-clinical-development-hematology-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Senior Medical Director, Clinical Development provides clinical leadership and is responsible for all clinical deliverables within the assigned section of a clinical program in Hematology Oncology with minimal supervision from Program Lead MD. Clinical deliverables may include individual protocols consistent with the Clinical Development Plans (CDP); clinical components of regulatory documents/registration dossier and brand related medical information, clinical communications and publications. This position offers the opportunity to give to a fast-growing, science-driven organization making a significant difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY or Warren, NJ</li><li>Travel percentage: 10% to relevant congresses/conferences</li></ul><h3>Discover your role:</h3><ul><li>Manages all operational aspects and drives execution of clinical programs in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates to ensure timely execution of assigned clinical deliverables within approved budget.</li><li>Leads interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards.</li><li>Ensures overall safety of the compound in collaboration with the Safety Lead for the assigned program.</li><li>Contributes to CRF’s, outsourcing specifications, data monitoring and validation plans, analysis plan for all trials to ensure consistency within the program.</li><li>Leads development of clinical sections of program level regulatory documents such as Investigators’ Brochures, briefing books, safety updates, IND/NDA submission documents, responses to Health Authorities questions with minimal input from Program Lead MD.</li></ul><h3>This role requires:</h3><ul><li>A M.D. degree, preferably with clinical training in a relevant disease area</li><li>More than 4 years' demonstrated experience in clinical research or drug development in an industry environment spanning clinical activities in Phases 1 through 4</li><li>Understand global regulatory environment including key regulatory agencies and approval processes</li><li>Have a strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out)</li><li>People Management experience preferred but not required.</li></ul><h3>#MDJobs, #MDJobsCD, #GDTherapeuticJobs #Hematology</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Third Party Risk Management]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47797]]></requisitionid>
    <referencenumber><![CDATA[R47797]]></referencenumber>
    <apijobid><![CDATA[r47797]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47797/director-third-party-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of Third Party Risk Management to join our Risk organization, supporting regional oversight and execution of our enterprise third-party risk management (TPRM) program. In this role, you will ensure third party risks across suppliers, service providers, and external partners are identified, assessed, mitigate, and escalated in alignment with our global TPRM framework, while collaborating with Procurement, Legal, Compliance, IP, and Information Security stakeholders.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Sleepy Hollow, NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Schedule: M-F 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Executes the global TPRM vision, framework, and operating model within the assigned region</p></li><li><p>Provides regional oversight for supplier risk activities, serving as the escalation point for material or emerging risks</p></li><li><p>Oversee the end-to-end third-party risk lifecycle, including onboarding, due diligence, ongoing monitoring, issue management, and offboarding</p></li><li><p>Partners with Compliance and Risk domain owners to support supplier assessments, issue remediation, and corrective action plans</p></li><li><p>Supports global governance bodies through regional insights and reporting</p></li><li><p>Drives adoption of automation, AI, analytics, and data-driven tools to improve efficiency and scalability of TPRM processes</p></li><li><p>Partners across Procurement, Legal, Compliance, IP, and Information Security to manage third-party risks holistically</p></li><li><p>Acts as a trusted regional advisor to business stakeholders on supplier risk matters</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Director Level: Bachelor's degree in a relevant field 12+ years of progressive experience in Third Party Risk Management, preferably within pharmaceutical, biotech, or other regulated industries</p></li><li><p>Previous people management experience required</p></li><li><p>Ability to leverage AI-enabled capabilities within approved platforms to support risk screening, monitoring, analysis, and reporting</p></li><li><p>Ability to partner with Procurement Technology and risk teams to streamline workflows and enhance risk insight while remaining aligned with governance and compliance requirements</p></li><li><p>Preferred/nice-to-have: Advanced degree or professional certification in risk, compliance, or a related field</p></li><li><p>Preferred/nice-to-have: Experience with TPRM technologies and risk monitoring platforms, including application of automation and AI-enabled tools within risk or compliance processes</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Recruiter - Italian speaking]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49222]]></requisitionid>
    <referencenumber><![CDATA[R49222]]></referencenumber>
    <apijobid><![CDATA[r49222]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49222/recruiter-italian-speaking/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Recruiter to join our Talent Acquisition team, reporting to the Associate Director, Talent Acquisition. In this role, you will lead full life cycle recruiting for assigned business groups while helping execute our broader TA strategy - crafting effective recruitment approaches and process improvements along the way. This is an opportunity to bring your multilingual, sourcing, and project management skills to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><p><strong>When & where</strong>:</p><p>Milan, Italy</p><p><strong>Discover your role:</strong></p><ul><li><p>Identify and attract top talent across international / global markets, using data-driven decisions to focus your time on the highest-impact priorities</p></li><li><p>Act as a strategic advisor to leaders, devising and deploying diverse talent strategies for assigned corporate roles</p></li><li><p>Directly source, approach, and engage passive candidates across LinkedIn Recruiter, professional networks, talent databases, industry events, and targeted outreach campaigns</p></li><li><p>Partner with third-party search firms as needed to ensure timely, quality hires</p></li><li><p>Work with the talent brand team to craft market-appropriate, culturally sensitive strategies that attract the right talent at the right time</p></li><li><p>Deliver great candidate and hiring team experiences by using data to optimise process and approach</p></li><li><p>Partner closely with HRBPs, HR Centres of Excellence, and business leadership to assess talent needs and translate workforce planning insights into action</p></li><li><p>Provide hiring data, metrics, and visualisation analytics that support smarter Talent Acquisition decisions</p></li><li><p>Stay current on government regulations, employment and privacy law, engaging with Company Counsel as needed</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Human Resources or a related field, plus 7+ years of experience in Recruiting / Talent Acquisition</p></li><li><p>Fluency in English, plus proficiency (written and spoken) in Italian</p></li><li><p>A track record of directly sourcing and engaging passive talent across digital platforms, professional networks, and industry events</p></li><li><p>Strong communication skills that resonate at every level of the organisation</p></li><li><p>Comfort balancing multiple, competing priorities in a fast-paced environment</p></li><li><p>Strong IT skills and a solid grasp of TA / HR metrics and data analysis</p></li><li><p>A collaborative approach to partnering with HRBPs, HR COEs, and business stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>57.375,00 € - 95.625,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Market Access Hematology Japan]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49826]]></requisitionid>
    <referencenumber><![CDATA[R49826]]></referencenumber>
    <apijobid><![CDATA[r49826]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49826/senior-manager-market-access-hematology-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Market Access Hematology Japan to join our market access team, supporting our Japan hematology business in a hybrid work model. In this role, you will drive launch, pricing, and reimbursement strategy while collaborating with commercial, medical affairs, HEOR, regulatory affairs, clinical, and global market access teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><p>Tokyo, Japan</p><p>Work model: Hybrid</p><br><h3>Discover your role:</h3><ul><li>Lead market access strategy for the hematology portfolio across Japan</li><li>Serve as the interface between global market access and the Japan affiliate</li><li>Drive NHI pricing and reimbursement submissions, including HTA dossiers</li><li>Execute price and HTA negotiations aligned to product strategy</li><li>Monitor reimbursement policy changes and assess business impact</li><li>Provide Japan-specific insights to shape value strategy and evidence plans</li><li>Represent Japan in global access forums and launch readiness reviews</li><li>You thrive in a collaborative, evolving environment with diverse stakeholders</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree required</li><li>8+ years of in-country market access experience</li><li>Strong knowledge of reimbursement systems, payer environments, cost comparator pricing methodology, and policy trends in Japan</li><li>Experience developing pricing strategy and reimbursement approaches</li><li>Excellent verbal and written communication skills</li><li>Business-level English and native-level Japanese</li><li>Strong project and process management skills with the ability to prioritize multiple tasks</li><li>Demonstrated initiative, critical thinking, and effectiveness in complex environments</li><li>Hematology launch or inline experience preferred</li><li>Proven negotiation experience with authorities in Japan preferred</li><li>Health Technology Assessment (HTA) experience and negotiation experience in Japan preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Responsible AI & Enterprise Governance]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49699]]></requisitionid>
    <referencenumber><![CDATA[R49699]]></referencenumber>
    <apijobid><![CDATA[r49699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49699/executive-director-responsible-ai-enterprise-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're looking for an Executive Director, Responsible AI & Enterprise Governance to join our fast-moving Enterprise Data & AI organization. You'll build and run our enterprise AI governance framework, setting the policies, standards, and controls that let Regeneron move fast with confidence, auditability, and trust. You'll partner closely with Legal, Compliance, and the CISO to keep AI use safe, compliant, and aligned with our values. This role reports to the SVP, Chief AI Officer, and offers the chance to shape governance as an accelerant for AI adoption, not a barrier to it.</p><br><h3><strong>When & where:</strong></h3><ul><li><strong>Location:</strong> This role is open to any of our Tri-State locations: Sleepy Hollow, NY, Tarrytown, NY, Armonk, NY, Warren, NJ or Cambridge, MA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Drive the enterprise AI governance program with senior business stakeholders across all Regeneron functions - AI governance forums, use case intake, and enterprise wide accountability</li><li>Lead the citizen development governance program - safe, auditable, enterprise-approved boundaries for non-technical builders</li><li>Define and own Regeneron's enterprise AI governance strategy across all model types, risk tiers, and deployment contexts</li><li>Build and lead a team of specialists across model validation, guardrails engineering, regulatory compliance, and citizen development governance</li><li>Establish the enterprise AI risk framework - taxonomy, classification standards, and control requirements across classical ML, foundation models, LLMs, fine-tuned models, and agentic systems</li><li>Set the technical assurance that includes validation frameworks, red-teaming, production monitoring, and pre-production sign-off gates</li><li>Own the end-end AI model lifecycle governance standard from ideation to deployment and monitoring</li><li>Drive LLM and agentic AI governance - grounding standards, retrieval integrity, tool use controls, autonomous action limits, and human-in-the-loop enforcement</li><li>Own GxP AI validation strategy and audit readiness across all regulated environments</li><li>Lead AI regulatory intelligence e.g. FDA, EMA, EU AI Act and emerging global frameworks, coordinated with Legal and business units to get ahead of compliance obligations</li><li>Partner at the executive level with Legal, Compliance, Regulatory Affairs, and CISO on regulatory interpretation, risk posture, and technical standards</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have led AI governance or technical risk functions in a complex, regulated industry and built the teams that execute them</li><li>Bring technical depth to set strategy and leadership range to hire and hold accountable the experts who implement it</li><li>Understand the distinct risk profiles of predictive, generative, and agentic systems and have governed them in production</li><li>Have driven GxP AI validation strategy in a life sciences or biopharma setting</li><li>Stay ahead of FDA AI/ML guidance, EU AI Act, and emerging frameworks — and convert them into enterprise action</li><li>Operate with credibility at the engineering level and the board level</li><li>See AI governance as a strategic capability that accelerates the business — and build it that way</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>A Bachelor's degree in a related field (advanced degree required for certain scientific or clinical positions)</li><li>17+ years of experience in AI governance, risk management, regulatory affairs, or compliance</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Precision Medicine (Clinical Diagnostics)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49909]]></requisitionid>
    <referencenumber><![CDATA[R49909]]></referencenumber>
    <apijobid><![CDATA[r49909]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49909/associate-director-precision-medicine-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution. This role owns CDx programs from early biomarker feasibility through clinical validation, regulatory submission, and launch — translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions. You'll work at the interface of biomarker science, clinical development, regulatory, and external IVD partners to ensure diagnostics keep pace with therapeutic milestones. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Uxbridge, United Kingdom (multiple locations are being considered for this role.)</p></li><li><p>Work model/flexibility: 3 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles (TPPs), defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays). </p></li><li><p>Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics.</p></li><li><p>Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints. </p></li><li><p>Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. </p></li><li><p>Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. </p></li><li><p>Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment. </p></li><li><p>Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). </p></li><li><p>Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. </p></li><li><p>Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. </p></li><li><p>8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. </p></li><li><p>Track record translating biomarker science into validated assays supporting drug approvals. </p></li><li><p>Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). </p></li><li><p>Ability to translate complex scientific and clinical data for cross-functional and executive audiences. </p></li><li><p>Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. </p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology-Louisville, KY]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44279]]></requisitionid>
    <referencenumber><![CDATA[R44279]]></referencenumber>
    <apijobid><![CDATA[r44279]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44279/medical-specialist-i-pulmonology-louisville-ky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where:</strong></p><ul><li><p>Field role</p></li><li><p>Louisville, KY</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49975]]></requisitionid>
    <referencenumber><![CDATA[R49975]]></referencenumber>
    <apijobid><![CDATA[r49975]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49975/director-international-commercialization-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Madrid, Spain - multiple locations are being considered for this role</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>96.000,00 € - 160.000,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Internal Auditor]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49834]]></requisitionid>
    <referencenumber><![CDATA[R49834]]></referencenumber>
    <apijobid><![CDATA[r49834]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49834/sr-internal-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Internal Audit Compliance & Operational Audit Specialist to join our Internal Audit team, supporting our compliance and governance programs in a hybrid work environment. In this role, you will contribute to the execution of the SOX 404 program, continuous auditing analytics, and operational audits while collaborating with accounting, technology, operational teams, and Internal Audit colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Review processes and functions within scope of the company's SOX 404 program and evaluate control effectiveness.</p></li><li><p>Develop and implement continuous auditing analytics to identify compliance, operational, and internal control weaknesses.</p></li><li><p>Partner with Internal Audit colleagues to design risk-based audit programs and support departmental deliverables.</p></li><li><p>Contribute to operational audits in accordance with Institute of Internal Auditors (IIA) standards, internal policies, and procedures.</p></li><li><p>Implement assigned audit sections independently with minimal supervision and accountability for deliverables.</p></li><li><p>Provide internal control guidance to business functions and departments to strengthen compliance practices.</p></li><li><p>Present audit findings and recommendations to auditees and engage confidently with middle management partners.</p></li><li><p>Support the preparation of audit recommendations and reports for Senior Management and the Audit Committee.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree in Accounting, Finance, Audit, Business, or a related field.</p></li><li><p>Minimum 3 years of relevant internal audit, external audit, compliance, or related experience.</p></li><li><p>Knowledge of SOX 404 compliance requirements, process reviews, and testing of internal controls.</p></li><li><p>Experience assessing compliance-related exposures, operational processes, and risk management practices.</p></li><li><p>Strong understanding of internal controls, governance frameworks, and operational audit methodologies.</p></li><li><p>Ability to find opportunities for operational efficiency improvements and practical risk mitigation solutions.</p></li><li><p>CPA and/or Certified Internal Auditor (CIA) certification preferred.</p></li><li><p>Experience with a Big Four accounting firm preferred.</p></li><li><p>Strong communication and presentation skills, including the ability to interact autonomously with middle management and present audit findings effectively.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager QA Auditor GCP Strategy]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48943]]></requisitionid>
    <referencenumber><![CDATA[R48943]]></referencenumber>
    <apijobid><![CDATA[r48943]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48943/senior-manager-qa-auditor-gcp-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><div><div><div><div><div><p><strong>Build our future together: </strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Audit Strategy, Global Development to join our Global Development Quality Assurance (GDQA), supporting our Global Development organization in a remote work mode. In this role, you will lead risk-based audit strategy programs and oversee compliance across therapeutic areas, studies, and audit activities while collaborating with Global Development teams, auditors, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p><p><strong>When & where: </strong></p><p>UK Remote - Ireland Remote </p><p><strong>Discover your role: </strong></p><ul><li><p>Lead risk-based audit planning across therapeutic areas and studies </p></li><li><p>Drive strategic audit programs using risk indicators from study teams </p></li><li><p>Ensure audits align with approved programs and scheduled timelines </p></li><li><p>Manage audit outcomes to identify trends and communicate risks </p></li><li><p>Represent quality assurance on complex cross-functional initiatives </p></li><li><p>Deliver reports and metrics to Global Development leadership </p></li><li><p>You collaborate effectively with stakeholders across global functions </p></li><li><p>You navigate ambiguity while prioritizing multiple complex activities </p></li><li><p>10-20% travel might be required</p></li></ul><p>This role requires: </p><ul><li><p>Bachelor’s degree with 8+ years of relevant industry experience </p></li></ul><ul><li><p>5+ years of GCP audit strategy or audit experience </p></li></ul><ul><li><p>Knowledge of FDA, EU, and ICH GCP regulations and guidance </p></li></ul><ul><li><p>Experience supporting or participating in regulatory inspections </p></li></ul><ul><li><p>Strong project management and stakeholder management capabilities </p></li></ul><ul><li><p>Excellent written and verbal communication skills with senior audiences </p></li></ul></div></div></div></div></div></div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager-Quality Assurance Auditor- GCP]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49361]]></requisitionid>
    <referencenumber><![CDATA[R49361]]></referencenumber>
    <apijobid><![CDATA[r49361]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49361/manager-quality-assurance-auditor-gcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, GCP Auditing to join our Global Development Quality Assurance (GDQA) team, supporting clinical development activities across our global portfolio. You will build strategic partnerships leading risk-based quality audits across investigator sites, service providers, and internal processes, ensuring our clinical studies meet the highest standards of GCP compliance, while collaborating with study teams, cross-functional partners, and regulatory colleagues around the world.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: US (Multiple locations are being considered for this role)<br>• Work model/flexibility: Remote<br>• Travel percentage: Ability to travel 30–40% of the time, both domestically and internationally</p><p><strong>Discover your role:</strong><br>• Own the end-to-end audit process — scheduling, preparing, conducting, reporting, and following up on routine and directed audits<br>• Lead a range of audit types across sites, vendors, license partners, and internal processes globally<br>• Apply deep knowledge of FDA, EU, and ICH regulations to independently resolve a variety of GCP compliance issues<br>• Represent GDQA on cross-functional teams and complex compliance projects spanning multiple departments<br>• Interpret regulations and quality standards, evaluating critical issues that fall outside existing guidance<br>• Support clinical study teams by developing and implementing risk-based audit strategies<br>• Step into regulatory inspections as part of the control or inspection room team when needed<br>• Mentor and help onboard new GDQA staff, sharing your auditing expertise</p><p><strong>This role requires:</strong><br>• Bachelor's degree with 6+ years of relevant industry experience including 4+ years of direct GCP audit experience. Background supporting risk-based audit strategy development for clinical studies<br>• Experience applying FDA and EU regulations including ICH E6 R3 and applicable standards. <br>• Ability to effectively manage multiple complex priorities and make complex decisions with a sense of urgency <br>• Strong track record of project management, stakeholder management, collaboration skills and negotiation of complex situations<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49495]]></requisitionid>
    <referencenumber><![CDATA[R49495]]></referencenumber>
    <apijobid><![CDATA[r49495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49495/manager-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p></div><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager</strong> to join our <strong>Regulatory Affairs Strategy Oncology</strong> team. The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Coordinate the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure </p></li><li><p>Assist in coordination and preparation for Agency meetings and associated briefing document preparation </p></li><li><p>Leads and tracks queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments </p></li><li><p>Provide representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum MD, PhD or PharmD degree along with 2+ years of regulatory experience.</p></li><li><p>We expect to see individuals have worked on filings, helped with developing regulatory related documents and engaged with external partners and authorities. </p></li><li><p>If you bring good understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices. </p></li><li><p>If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred </p></li><li><p>If you have a high attention to detail; ability to coordinate and prioritize assigned projects according to company goals </p></li><li><p>You bring strong interpersonal skills both written and verbally </p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Engineer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49544]]></requisitionid>
    <referencenumber><![CDATA[R49544]]></referencenumber>
    <apijobid><![CDATA[r49544]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49544/principal-it-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are building a world-class Global Capability Center (GCC) in Hyderabad that serves as a strategic hub for innovation, technology, and business operations. We are seeking a Senior Manager, Strategy Planning & Operations to partner closely with GCC leadership and global stakeholders in driving operational excellence, external partnerships, ecosystem engagement, and strategic growth initiatives. This role will play a critical part in shaping the GCC's long-term value proposition through government and industry engagement, university partnerships, performance management, and cross-functional operational leadership.</p><p><strong>When & Where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Serve as a strategic advisor and operational partner to GCC leadership, driving initiatives that advance organizational growth, collaborator engagement, and business performance.</p></li><li><p>Build and maintain strong relationships with government agencies, industry associations, and regulatory bodies to support GCC growth strategies and policy engagement.</p></li><li><p>Represent the GCC at industry forums, leadership summits, and external events while seeing opportunities for collaboration, innovation, and ecosystem partnerships.</p></li><li><p>Establish and manage relationships with leading universities and academic institutions to strengthen talent pipelines, research collaborations, internship programs, and employer branding initiatives.</p></li><li><p>Partner with Talent Acquisition and University Relations teams to develop and implement campus engagement strategies aligned with workforce planning objectives.</p></li><li><p>Develop and own GCC performance dashboards, tracking metrics such as headcount growth, attrition, productivity, cost efficiency, hiring outcomes, and strategic breakthroughs.</p></li><li><p>Lead monthly and quarterly business reviews with GCC and global leadership teams, providing insights, recommendations, and operational performance updates.</p></li><li><p>Identify operational and strategic risks across the GCC and coordinate mitigation plans with HR, Finance, IT, Legal, Compliance, Facilities, and business collaborators.</p></li><li><p>Define and communicate the GCC value story by demonstrating business impact, innovation outcomes, capability growth, and operational excellence to global headquarters.</p></li><li><p>Partner with Finance to develop cases, return on investment analyses, Total Cost of Ownership (TCO) assessments, and annual value-delivery reports.</p></li><li><p>Drive the GCC operating rhythm by managing leadership reviews, governance forums, town halls, quarterly business reviews, and critical initiative tracking.</p></li><li><p>Prepare leadership communications, executive briefings, presentations, and materials for high-priority engagements including board reviews, industry forums, and leadership meetings.</p></li><li><p>Manage strategic projects from planning through execution, ensuring timelines, breakthroughs, budgets, risks, and collaborator expectations are effectively managed.</p></li><li><p>Champion continuous improvement initiatives by identifying operational inefficiencies and implementing scalable solutions that enhance organizational effectiveness.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MBA or equivalent experience or equivalent postgraduate degree from a reputed institution; Tier-1 institution preferred.</p></li><li><p>8-10+ years of progressive experience in strategy, business operations, consulting, program management, or GCC/captive center leadership environments.</p></li><li><p>Demonstrated experience working with government agencies, industry associations, regulatory bodies, or external collaborator ecosystems.</p></li><li><p>Experience developing and managing university partnership programs, talent ecosystem initiatives, or workforce development collaborations.</p></li><li><p>Strong expertise in KPI development, dashboard reporting, business reviews, and executive-level performance reporting.</p></li><li><p>Financial and business insight with the ability to translate operational performance into strategic and value-based narratives.</p></li><li><p>Experience managing complex projects across multiple cross-functional collaborators in a matrixed environment.</p></li><li><p>Strong analytical capabilities with proficiency in PowerPoint, Excel, business intelligence tools, and executive storytelling.</p></li><li><p>Exceptional communication, executive presence, and stakeholder management skills.</p></li><li><p>High emotional intelligence and the ability to influence across diverse internal and external partner groups.</p></li><li><p>Ability to navigate ambiguity, prioritize competing demands, and deliver results in a fast-paced environment.</p></li><li><p>Strong understanding of the Hyderabad GCC ecosystem, technology landscape, and industry trends is highly desirable.</p></li><li><p>Strategic problem solver with a bias for execution, continuous improvement, and measurable business impact.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 14 Aug 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Development Program Management- Oncology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49992]]></requisitionid>
    <referencenumber><![CDATA[R49992]]></referencenumber>
    <apijobid><![CDATA[r49992]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49992/senior-director-development-program-management-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Development Program Management to join our Portfolio and Program Management team, supporting our Oncology in a hybrid capacity. In this role, you will lead program strategy while collaborating with cross-functional teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY or Warren, NJ</li><li>Hybrid</li><li>Travel percentage: 25%</li></ul><h3>Discover your role:</h3><p>We are seeking a highly experienced and dynamic Senior Director Development Project Manager to join our team. The successful candidate will primarily be responsible for identifying and developing a team of manager through associate director ready program managers. Additionally, the successful candidate will provide operational leadership, direction, and support to assigned small and/or low to medium complexity development program(s).</p><h3><strong>Team</strong> <strong>Leadership</strong> <strong>and Management</strong> <strong>(Primary responsibility)</strong>:</h3><ul><li>Recruit, hire, build and lead a team of high performing, early-career program managers.</li><li>Lead & advance talent-- from manager to associate-director ready talent-- with emphasis on developing, improving, or enhancing PM capabilities, processes & initiatives.</li><li>Identify and assess development needs of direct reports; Ensure direct reports have actionable development plans and receive ongoing coaching and feedback to enable growth and future leadership</li><li>Establish and maintain comprehensive training and development curriculum for program managers that aligns with department goals and career ladder.</li><li>Build project allocation model and process to support the pipeline and development of direct reports.</li><li>Collaborate with portfolio management to understand longer range resourcing needs and develop plan to address.</li></ul><h3><strong>Project Leadership and Management: </strong></h3><ul><li>Partner with the Global Program Head on small and/or low to medium complexity program(s) to drive Strategic Program Teams, leading the management and execution from preclinical through late development and life cycle management.</li><li>Develop and ensure delivery of comprehensive integrated plans, including timelines and budgets, and ensure alignment with company goals.</li></ul><h3><strong>Continuous Improvement</strong>:</h3><ul><li>Identify opportunities for process improvements and implement best practices in project management. Proactively share lessons learned within the team and across the organization.</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree required. Master's preferred. Minimum of 15+ years' experience relevant broad project / program management experience required, preferably in the pharmaceutical or related industry</li><li>Have extensive experience in Pharma R&D project management, a deep understanding of the end-to-end drug development process and a proven ability to deliver results</li><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels both internal and external to the company in order to establish credibility with professionals on the project teams.</li><li>Have strong presentation and critical thinking skills.</li><li>Actively promote constructive interactions among team members to address difficult situations.</li><li>Resolve and negotiate conflicts or problems with tact, diplomacy and composure.</li><li>Handle multiple projects and priorities with exceptional organizational and time management skills</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 14 Aug 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Laboratory Assistant II, Product Biochemistry]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50019]]></requisitionid>
    <referencenumber><![CDATA[R50019]]></referencenumber>
    <apijobid><![CDATA[r50019]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50019/laboratory-assistant-ii-product-biochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Laboratory Assistant II</strong> to join our Product Biochemistry (PB) team, part of the Product Analytical and Process Development (PAPD) department, supporting the lab operations group. In this role, you will help manage and optimize all aspects of the lab environment — including lab management, process optimization, compliance and safety, resource allocation, and coordination & communication — while collaborating with the broader PB team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><strong>Shift Requirements:</strong> Full-time</li><li><strong>Location:</strong> On-site laboratory setting</li><li><strong>Flexibility & travel:</strong> No travel; consistent on-site presence required to support routine lab operations</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Support lab operations by receiving packages and entering product info into the Electronic Notebook (ELN)</li><li>Manage sample shipment requests (internal, external, international) and maintain documentation</li><li>Assist with sample distribution workflows and manage distribution points</li><li>Organize, catalog, and reconcile sample inventory and freezers</li><li>Assist with managing non-database aliquot inventory and provide auxiliary support for aliquoting workflow as needed</li><li>Coordinate biannual pipette calibrations</li><li>Participate in LIMS database development, testing, and troubleshooting</li><li>Learn and adapt to new laboratory practices (SOPs, protocols, procedures, etc.) with supervision</li><li>Update and manage shared document libraries and functional Excel worksheets</li><li>Prioritize and manage tasks in a high-throughput laboratory to ensure smooth operation</li><li>Suggest key process improvement opportunities and help implement strategies to increase speed and efficiency</li><li>Support additional activities as they arise to continuously support PBG through future growth and expansion</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is a high-throughput laboratory role requiring the ability to lift and carry packages and supplies as needed.</li><li>Willingness to learn and adapt to new laboratory practices, tasks, and responsibilities, with supervision, is required.</li></ul><br><h3><strong>Let's find out if we're a fit:</strong></h3><p><strong>Must-haves:</strong></p><ul><li>High school diploma or associate degree with 0–3 years' experience</li><li>Excellent organization, communication, and collaboration skills; ability to work well within a team and individually</li><li>Ability to lift and carry packages and supplies as needed</li></ul><p><strong>Preferred / nice-to-haves:</strong></p><ul><li>Service-oriented mindset and desire to provide quality customer service</li><li>Interest in science and strong attention to detail</li><li>Willingness to learn new tasks and responsibilities, with a solid understanding of workplace technologies</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$26.35 - $41.15]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager of Site Supply Planning and Scheduling]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49831]]></requisitionid>
    <referencenumber><![CDATA[R49831]]></referencenumber>
    <apijobid><![CDATA[r49831]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49831/manager-of-site-supply-planning-and-scheduling/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Site Supply Planning and Scheduling Manager to join our IOPS Supply Chain Planning team, overseeing end-to-end production planning across Regeneron's internal and external manufacturing network for both clinical and commercial portfolios. In this role, you will drive master production scheduling, finite scheduling, batch management, and capacity planning — while serving as the planning liaison for site teams and collaborating with Operations, Finance, Regulatory, and Program Management. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Oversee the creation and execution of the site master production schedule, ensuring reliable supply of clinical and commercial products based on demand forecasts, program strategies, and operational capabilities</li><li>Act as the planning liaison for site teams, accurately reflecting manufacturing capabilities, constraints, and performance in the broader supply plan; proactively identify and resolve conflicts</li><li>Lead finite scheduling for production and post-production activities, managing coordination with external departments for maintenance, cleaning, validation, and microbial monitoring</li><li>Steward produced batches through post-production milestones, tracking batch statuses and mitigating risks to downstream supply nodes</li><li>Lead scenario-based planning and risk assessments to evaluate supply and business risks; implement business continuity plans to ensure uninterrupted supply</li><li>Manage capacity project portfolio, recommending capital expenditures and aligning implementation plans with program, regulatory, and supply strategies</li><li>Implement real-time monitoring systems for schedule adherence; develop mechanisms to improve communication to and from the production floor</li><li>Champion continuous improvement initiatives to transform business processes, reduce lead times, manage costs, and enhance overall operational efficiency</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Business, Engineering, Supply Chain Management, or a related field</li><li>Associate Manager: 6+ years of progressive experience in supply chain, manufacturing, or operations planning within biotech, pharmaceutical, or life sciences</li><li>Manager: 7+ years of progressive experience in supply chain, manufacturing, or operations planning within biotech, pharmaceutical, or life sciences</li><li>Demonstrated experience in an end-to-end planning role in a cGMP manufacturing environment with a strong understanding of regulatory requirements</li><li>Expertise in production planning, capacity planning, and supply chain management concepts; experience with ERP/MRP/APS and project management systems a plus</li><li>Proven track record managing complex, cross-functional projects and portfolios; relevant certifications such as PMP, APICS, or Lean Six Sigma a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Hematology Thought Leader Liaison (TLL) - Northeast]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49942]]></requisitionid>
    <referencenumber><![CDATA[R49942]]></referencenumber>
    <apijobid><![CDATA[r49942]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49942/associate-director-hematology-thought-leader-liaison-tll-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Hematology Thought Leader Liaison (TLL) Northeast is a field-based, non-sales position on Regeneron’s Commercial Hematology Marketing team. It will be focused on enhancing and improving interactions with key external US hematology thought leaders at academic centers and leading community practices for our Hematology bispecific.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Oncology/Hematology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><h3>When & where:</h3><ul><li>Must reside in one of the following states:</li><li>Pennsylvania, Delaware, New York, New Jersey, Connecticut, New Hampshire, Maine, Vermont, Massachusetts</li><li>Must be able to travel 60%-80% of time within the territory</li></ul><h3>Discover your role:</h3><ul><li>The Hematology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau program placement and execution, which may include identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10 years of work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in hematology/oncology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry</li><li>Experience with physician-administered biologics preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 09:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Director Rare Disease Commercial - EU4+UK Region]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49844]]></requisitionid>
    <referencenumber><![CDATA[R49844]]></referencenumber>
    <apijobid><![CDATA[r49844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49844/sales-director-rare-disease-commercial-eu4plusuk-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Sales Director Rare Disease Commercial EU4+UK Region</h3><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sales Director Rare Disease</strong> to join our International Rare Disease team, supporting our EU4+UK region. In this role, you will lead a high-performing field organization and drive commercial execution across our rare disease portfolio while collaborating with cross-functional teams and regional leadership. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Location: Paris, France - Office based, Hybrid.</p><h3><strong>Discover your role:</strong></h3><ul><li>Lead a sales team across EU4+UK to deliver company objectives.</li><li>Drive account targeting, segmentation, and multichannel customer engagement.</li><li>Set performance objectives and lead coaching, development, and succession planning.</li><li>Align incentive compensation plans with brand strategies and targets.</li><li>Partner with Commercial Operations on training, analytics, KPIs, Veeva CRM, and territory alignment.</li><li>Provide field insights on customer feedback, patient journey barriers, and competitive intelligence.</li><li>Partner with cross-functional team members to address market trends and dynamics.</li><li>You champion excellence, accountability, and patient-centricity across the organization.</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree required.</li><li>Advanced degree in life sciences, pharmacy, medicine, or business strongly preferred.</li><li>Minimum 10 years’ experience in the pharmaceutical or biotechnology industry.</li><li>Minimum 3 years in a first-line field sales management role.</li><li>Proven success hiring, mentoring, developing, and retaining high-performing teams.</li><li>Experience in rare disease, specialized medicines, or gene therapy/ATMP commercialization preferred.</li><li>Ability to operate within sophisticated multi-stakeholder account environments.</li><li>Knowledge of market access and reimbursement frameworks across EU4+UK markets.</li><li>Ability to mentor teams on value-based and access-oriented payer engagement.</li><li>Experience with Veeva CRM, Salesforce effectiveness tools, data analytics, and digital promotion.</li><li>Proficiency in English and one additional European language highly desirable (French, German, Italian, or Spanish)</li><li>Knowledge of EFPIA and applicable national pharmaceutical industry codes.</li><li>Ability to travel 50% or more across EU4+UK and hold a valid driving licence.</li><li>Established KOL relationships in rare metabolic, musculoskeletal, or hearing loss areas are desirable.</li><li>Strong leadership, communication, and interpersonal skills in multicultural environments.</li></ul><div></div><p><strong>Salary range (annually):</strong> 86,550€ - 144,250€ </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 14 Aug 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Partnerhsip and Trial Optimization]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49872]]></requisitionid>
    <referencenumber><![CDATA[R49872]]></referencenumber>
    <apijobid><![CDATA[r49872]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49872/director-global-partnerhsip-and-trial-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Director, Global Development Strategic Partnerships to identify, establish, and manage strategic relationships with external organisations and institutions. You will coordinate across a matrix of teams to create partnership opportunities that strengthen clinical development, clinical research, and Regeneron’s broader R&D objectives. You will support partnership agreements from identification and evaluation through contract drafting, execution, and ongoing relationship management, working closely with internal leaders to maintain collaboration, continuity, and alignment.</p><p><strong>When & where</strong></p><p>Uxbridge (hybrid).</p><p><strong>Discover your role</strong></p><ul><li><p>Develop a long-term, company-wide strategy for working with external organisations to support clinical trials and translational and basic research.</p></li><li><p>Identify and evaluate external partners based on agreed organisational needs, opportunities, and capability gaps.</p></li><li><p>Drive the evaluation and coordination of partnership opportunities, engaging internal experts when additional support is required.</p></li><li><p>Coordinate new opportunities with existing and prospective partner organisations.</p></li><li><p>Support contract drafting and execution while remaining connected to strategic relationships throughout the agreement lifecycle.</p></li><li><p>Manage and track external partnership opportunities in collaboration with project management and other external-facing colleagues.</p></li><li><p>Build consistent communication channels with internal and external partners to maintain continuity, alignment, and productive relationships.</p></li><li><p>You work collaboratively across functions to prioritise strategic partnerships and identify opportunities for innovation and efficiency.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Previous experience and a deep understanding of the drug development process.</p></li><li><p>A proven track record of developing and maintaining partner relationships at all organisational levels.</p></li><li><p>Strong existing relationships and a positive reputation within the life sciences industry, particularly with academic medical centres and large health systems.</p></li><li><p>Strong business and financial management acumen, with experience in strategic planning and tactical execution.</p></li><li><p>The ability to manage and prioritise multiple tasks and projects with urgency while working within a matrix organisation.</p></li><li><p>Outstanding written, verbal, presentation, and consensus-building skills, with the ability to communicate accurately and concisely.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 10:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs- Respiratory (Arizona/New Mexico)]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50004]]></requisitionid>
    <referencenumber><![CDATA[R50004]]></referencenumber>
    <apijobid><![CDATA[r50004]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50004/associate-director-field-medical-affairs-respiratory-arizonanew-mexico/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs, to join our Respiratory team, supporting healthcare providers and payers in a field-based role. In this role, you will establish and maintain scientific exchange with medical specialists and decision-makers, ensuring accurate and timely dissemination of clinical data on in-line and pipeline products, while collaborating with Global Medical Affairs leadership and clinical research investigators.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Field based in Arizona and New Mexico (residency in the Phoenix area preferred; residency in territory required)<br>Discover your role:<br>• Engage in scientific discussions with Healthcare Professionals and payers, aligned with Medical Affairs objectives.<br>• Demonstrate deep scientific expertise in assigned molecules/products and therapeutic area.<br>• Build and nurture relationships with key external scientific and medical specialists across the region.<br>• Stay ahead of evolving healthcare trends within the Dermatology therapeutic landscape.<br>• Shape and implement local medical strategy in line with Global Medical Affairs direction and timelines.<br>• Support clinical research sites and investigators. <br>• Deliver clinical and health economic information that enhances the appropriate use of our products.<br>• Communicate scientific and clinical information ethically, accurately, and in a customer-focused manner.</p><p><strong>This role requires:</strong><br>• Clinical/Science Degree (e.g., MD, PharmD, PhD) with a minimum of 5 years of related work experience (clinical, managed care, or industry)<br>• Experience as a Medical Science Liaison within Immunology is required. Respiratory is preferred.<br>• Strong ability to communicate and disseminate scientific and clinical data.<br>• Residency within the territory <br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Study Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50053]]></requisitionid>
    <referencenumber><![CDATA[R50053]]></referencenumber>
    <apijobid><![CDATA[r50053]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50053/clinical-study-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Specialist to join our Clinical Trial Management team, supporting our clinical trial execution in a hybrid role. In this role, you will provide technical and administrative study support while collaborating with clinical study teams, sites, and third-party vendors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Uxbridge (Hybrid)<br> </p><p><strong>Discover your role:</strong></p><ul><li><p>Deliver analysable study reports and metrics to the Clinical Study Lead.</p></li><li><p>Coordinate study meetings, agendas, presentations, minutes, training materials, and investigator meetings.</p></li><li><p>Collate feasibility and site-selection data, including site usability database reviews.</p></li><li><p>Facilitate document reviews and maintain version-controlled regulatory, pharmacy, and laboratory manuals.</p></li><li><p>Track site activation, enrolment, monitoring visits, registry postings, and scheduled compliance reports.</p></li><li><p>Reconcile the Trial Master File and track close-out documents, product reconciliation, and CRA visits.</p></li><li><p>Maintain SharePoint sites, site contacts, BDRM line listings, and third-party vendor oversight.</p></li><li><p>You proactively identify issues, escalate delays, and recommend departmental process improvements.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree or five years of relevant experience.</p></li><li><p>At least two years of industry-related experience.</p></li><li><p>An advanced related degree with one to two years of relevant experience is preferred.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 04:26:31 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[PharmD Program Associate - Clinical Operations & Program Management]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50231]]></requisitionid>
    <referencenumber><![CDATA[R50231]]></referencenumber>
    <apijobid><![CDATA[r50231]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50231/pharmd-program-associate-clinical-operations-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> </p><p>The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles. </p><p>This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. </p><p><strong>When & where:</strong> </p><ul><li><p><strong>Location:</strong> Tarrytown, NY </p></li><li><p><strong>Travel percentage:</strong> Up to 15% </p></li></ul><p><strong>Program Tracks:</strong> <br>The program is comprised of a 24-month rotational experience within one of the following tracks: </p><ul><li><p><strong>Clinical Operations & Program Management </strong></p></li><li><p>Clinical Sciences </p></li><li><p>Regulatory Strategy </p></li><li><p>Regulatory Labeling & Advertising/Promotion </p></li><li><p>Safety Sciences </p></li></ul><p>Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program. </p><p><strong>Clinical Operations & Program Management </strong>– Associates will support the management of clinical trials by actively contributing to key activities related to trial set-up, execution, conduct and close out. In program management, the Associates will broaden their scope and participate in activities related to strategic decision making, governance interactions and integrated drug development planning.</p><p><strong>Discover your role:</strong> </p><ul><li><p>Drafting documents integral to clinical sites and regulatory submissions </p></li><li><p>Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others </p></li><li><p>Managing third-party vendors and maintaining timelines of key results </p></li><li><p>Developing regulatory strategies for clinical development programs </p></li><li><p>Analyzing safety data to characterize the safety profile of products throughout their development lifecycle </p></li><li><p>Working with program mentors to improve skills to reach professional goals better </p></li><li><p>Opportunities to travel to clinical sites and/or meetings with health authorities </p></li></ul><p><strong>This role requires:</strong> </p><ul><li><p>Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates within a life science related area of study may also be considered. </p></li><li><p>You must have completed your PharmD and/or PhD degree by Summer 2027 </p></li><li><p>Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus </p></li><li><p>Exposure or familiarity with evaluating clinical trials, scientific literature and data </p></li><li><p>You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences You are eligible to work in the U.S. on a permanent basis </p></li></ul><p><strong>Application Details:</strong> </p><p><strong>When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference. </strong></p><p><strong>Applications Accepted: August 24th, 2026 - September 11th, 2026</strong> <br>For more information on the tracks, program, and interview process, please refer to the brochure. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Digital & Technology - HR, Corporate Affairs, Business Development, Corporate Strategy]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50014]]></requisitionid>
    <referencenumber><![CDATA[R50014]]></referencenumber>
    <apijobid><![CDATA[r50014]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50014/executive-director-digital-technology-hr-corporate-affairs-business-development-corporate-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is a leading biotechnology company built on a simple but powerful mission: to use the power of science to bring new medicines to patients, over and over again. Founded and led by physician-scientists, we've turned that mission into one of the industry's most productive pipelines, nearly all of it homegrown in our own laboratories, powered by proprietary technologies like our VelociSuite® platform. From Dupixent and EYLEA to a rapidly expanding portfolio across oncology, cardiovascular and metabolic disease, neuroscience, and rare disease, our science is reaching millions of patients worldwide, and we're just getting started.</p><p>As we invest billions in new manufacturing capacity, expand our global footprint, and build the next generation of digital and technology capabilities to match the scale of our ambition, Regeneron offers a rare combination: the resources and reach of an industry leader, paired with the energy, curiosity, and relentless focus on invention of a company still writing its next chapter. This is a place where technology doesn't just support the business, it accelerates the science that changes patients' lives.</p><p><em>This role will sit in our Sleepy Hollow, NY office 4 days per week.</em></p><p><strong>Role Description</strong></p><p>The Executive Director will lead the technology strategy and roadmap supporting HR, Corporate Affairs, Business Development, Corporate Strategy, and Strategic Alliances at Regeneron, including ownership of the Workday platform and related enterprise solutions. Partnering closely with senior executives, this leader aligns technology investments with talent, partnership, and strategic business objectives. The role has significant influence over how the company manages its workforce, external relationships, and strategic initiatives through technology. Additionally, the individual serves as the primary technology advisor and executive spokesperson for these functions.</p><p><strong>What You'll Lead</strong></p><ul><li>Lead the technology strategy and multi-year roadmap for HR, Corporate Affairs, Business Development, Corporate Strategy, and Strategic Alliances, aligning investments with enterprise priorities.</li><li>Own and optimize the HR technology portfolio, including Workday and related platforms supporting talent acquisition, employee experience, learning, workforce planning, and people analytics.</li><li>Deliver technology solutions for business development, strategic planning, alliance management, partner collaboration, and AI-enabled opportunity intelligence.</li><li>Build and lead a high-performing global technology organization, developing talent and driving execution across complex business functions.</li><li>Drive measurable business outcomes through improved hiring, onboarding, HR service delivery, deal execution, alliance effectiveness, automation, system reliability, and productivity.</li><li>Modernize and standardize technology platforms, processes, operating models, and data capabilities across supported functions.</li><li>Advance AI, automation, workforce analytics, and decision intelligence strategies to improve business performance and user experience.</li><li>Oversee vendor management, technology investments, Workday governance, cybersecurity, data privacy, and platform resilience to ensure secure, scalable, and high-value solutions.</li></ul><p><strong>What You Bring</strong></p><ul><li>BS/BA in Computer Science, Information Systems, Human Resources, or a related field required; MS or MBA preferred.</li><li>17+ years of progressive HR technology leadership, including large-scale Workday (HCM) programs.</li><li>Deep expertise in Workday architecture, release strategy, and integrations.</li><li>Familiarity with technology needs of business development, corporate strategy, or alliance management functions is a plus.</li><li>Proven ability to influence senior leaders, set standards across functional areas, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -MIAMI, FL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48032]]></requisitionid>
    <referencenumber><![CDATA[R48032]]></referencenumber>
    <apijobid><![CDATA[r48032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48032/medical-account-specialist-ii-neurology-miami-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Miami]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Miami (Metro), FL</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -  SAINT LOUIS, MO]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48055]]></requisitionid>
    <referencenumber><![CDATA[R48055]]></referencenumber>
    <apijobid><![CDATA[r48055]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48055/medical-account-specialist-ii-neurology-saint-louis-mo/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[St. Louis]]></city>
    <state><![CDATA[Missouri]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: St. Louis (Metro) MO</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology - Alberta]]></title>
    <date><![CDATA[Tue, 09 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47980]]></requisitionid>
    <referencenumber><![CDATA[R47980]]></referencenumber>
    <apijobid><![CDATA[r47980]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47980/sales-specialist-immunology-alberta/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a S<strong>pecialty Representative, Immunology in Alberta </strong>to join our International Immunology team, supporting our Canada in a hybrid work mode. In this role, you will drive sales growth and deliver impactful customer engagement while collaborating with regional teams, business partners, and management. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Alberta, Canada</li><li>Field based</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and optimally implementing sales & marketing plan.</li><li>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</li><li>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</li><li>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</li><li>Leverage all communication channels including digital channels, in collaboration with other functions, to achieve the best possible share of voice in the market.</li><li>Report results and developments proactively and clearly to the Immunology leadership team</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree</li><li>Minimum 5 years’ experience as a Specialty Pharmaceutical Representative</li><li>Experience working within a commercial alliance environment is desirable</li><li>Proven track record to run accounts and meet performance objectives</li><li>Experience engaging healthcare professionals using multiple communication channel</li><li>Ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</li><li>Working in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</li><li>Balancing multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</li><li>You can operate optimally in a “start-up” model as this is a completely new team.</li><li>Regular travel and have a valid driver's license. Proficiency in English is required.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - PHILADELPHIA NORTH, PA]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48013]]></requisitionid>
    <referencenumber><![CDATA[R48013]]></referencenumber>
    <apijobid><![CDATA[r48013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48013/medical-account-specialist-ii-neurology-philadelphia-north-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Philadelphia North (Metro), PA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager  - Neurology (Northeast)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48125]]></requisitionid>
    <referencenumber><![CDATA[R48125]]></referencenumber>
    <apijobid><![CDATA[r48125]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48125/field-reimbursement-manager-neurology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Boston]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Neurology Field team supporting the successful launch and adoption of an HCP-administered rare disease therapy. You will serve as a reimbursement and access expert across buy & bill, specialty pharmacy and alternate sites of care. In this role, you will support providers throughout all facets of the reimbursement cycle including coverage, coding, product acquisition, available patient support services and site-of-care decision making to enable sustained patient access in a competitive rare disease environment.</p><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: Boston, (Metro) MA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and execute account-specific access and reimbursement plans that support product launch, optimize site of care (alignment of payer policy + patient needs) and build reimbursement confidence with customers (e.g. MD and staff) & support continued patient access.</li><li>Proactively educate accounts on patient support services and collaborate with Patient Services to support efficient patient onboarding, therapy initiation and ongoing treatment.</li><li>Develop collaborative relationships with Sales, Patient Services, Account Directors and Medical to align access strategy and remove barriers to therapy initiation.</li><li>Partner cross-functionally to ensure consistent, accurate REMS communication and field execution</li><li>Support coordination between provider offices, specialty pharmacy and infusion sites</li><li>Guide healthcare professionals in resolving access challenges including prior authorizations, denials, appeals and payer site-of-care restrictions in a manner that follows Regeneron policies and processes.</li><li>Anticipate and adapt to evolving launch dynamics, payer policies and distribution pathway changes.</li><li>Demonstrate proactive planning and time management skills by the efficient and effective coverage of your assigned FRM Territory.</li><li>Establish relationships with access champions (providers, administrators, office staff, financial coordinators) to support access readiness and ongoing therapy delivery.</li><li>Proactively update customer son payer policy evolution, coding updates (e.g. J-code progression), and site-of-care management treads.</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred).</li><li>We are also expecting you to have experience across buy & bill and specialty pharmacy distribution models, including white bagging and site of care management.</li><li>Rare disease and experience supporting product launches strongly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Fill/Finish Associate (Internal Fill/Finish MFG)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46367]]></requisitionid>
    <referencenumber><![CDATA[R46367]]></referencenumber>
    <apijobid><![CDATA[r46367]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46367/fillfinish-associate-internal-fillfinish-mfg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Fill/Finish Associate. The Fill/Finish Associate performs all duties related to the production and support of drug product manufacturing. Works individually, and as part of a team, to support and perform operations to maintain formulation, filling, assembly, labeling and cartoning/packing equipment for parenteral biological products. Seeks to understand and develops proficiency in processes or procedures of increasing complexity.<br> </p><p>When & where:</p><ul><li><p>We offer multiple shifts that are 4 working days (10 hours) to support 24/7 production</p></li><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Occasional flexibility may be requested for on-call schedule/weekend work</p></li></ul><p>What you'll do:</p><ul><li><p>Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges within isolators or other cleanroom environments; assemble filled product into syringes and autoinjectors; and run state-of-the-art packaging lines to label and configure product for distribution.</p></li><li><p>Monitor production operations using process controls and feedback systems (pneumatics, robotics, manual checks, and PLCs) to ensure throughput, quality, and compliance.</p></li><li><p>Perform equipment changeovers, cleaning, handling, and installation of interchangeable parts; maintain clean, safe, and inspection-ready workspaces and equipment.</p></li><li><p>Maintain gowning qualification, adhere to aseptic/cleanroom behaviors, and perform environmental monitoring and sampling as required.</p></li><li><p>Create, follow, and improve SOPs and operating procedures aligned with cGMP and regulatory expectations; ensure compliance during execution and promptly escalate nonconformities.</p></li><li><p>Record and review GMP data with ALCOA principles (accurate, legible, attributable, contemporaneous); reconcile product and controlled materials; and ensure complete training documentation.</p></li><li><p>Utilize electronic systems (e.g., MES/eBR, LIMS, training systems, and Microsoft Office) to support manufacturing operations and documentation.</p></li><li><p>Travel domestically and internationally as needed to support production or technology transfer activities.</p></li></ul><p>The environment and physical rhythms of the role:</p><ul><li><p>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p>Let's find out if we're a fit:</p><ul><li><p>HS diploma/ GED</p></li><li><p>Or AS, BS or BA in Life Sciences or related field</p></li><li><p><em>Level is determined on qualifications relevant to the role. </em></p></li></ul><p>Thrive today. Grow Tomorrow.</p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family care benefits</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$16.44 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Toxicologist]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47420]]></requisitionid>
    <referencenumber><![CDATA[R47420]]></referencenumber>
    <apijobid><![CDATA[r47420]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47420/senior-toxicologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from her/his direct supervisor working effectively within cross-functional project teams. The Sr. Toxicologist will demonstrate a thorough understanding of GLP regulations and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the design, conduct, interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/toxicology studies in rodent and non-rodent safety models. The Sr. Toxicologist will provide primary authorship of all regulatory documentation required for submission packages, demonstrating excellent problem solving and communication skills (written and verbal).</p><p>Experience with multiple therapeutic modalities preferred, including antibody, oligonucleotide, and genetherapy products.</p><p><strong>JOB RESPONSIBILITIES:</strong></p><ul><li><p>Represent toxicology on global research and development project teams communicating non-clinical safety assessment strategy.</p></li><li><p>Coordinate cross-department execution of the experimental plan including program budgets, and timing of toxicology studies in relation to regulatory and clinical milestones.</p></li><li><p>Work with study monitoring group to coordinate, design, monitor, and report toxicology and safety pharmacology studies at contract research organizations.</p></li><li><p>Communicate toxicology study findings, including relevant interpretation, to project teams and management.</p></li><li><p>Contributing to non-clinical sections of regulatory documents including IND and NDA submissions.</p></li><li><p>Maintain currency with GLP regulations and ICH, FDA and EMEA non-clinical safety guidelines.</p></li><li><p>Keep up with the latest scientific developments by reading the current literature and attending conferences.</p></li></ul><p><strong>JOB REQUIREMENTS:</strong></p><ul><li>Advanced degree (e.g. PhD, DVM) in pharmacology, toxicology or closely related biological science along with 3-5 years relevant pharmaceutical industry experience, or Master’s Degree + ≥ 10 years relevant pharmaceutical industry</li><li>Experience in designing, monitoring and interpreting non-clinical safety studies.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Field Excellence & Enablement]]></title>
    <date><![CDATA[Wed, 22 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49349]]></requisitionid>
    <referencenumber><![CDATA[R49349]]></referencenumber>
    <apijobid><![CDATA[r49349]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49349/senior-director-field-excellence-enablement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>We are seeking a visionary and strategic senior leader with a wealth of diverse experience to work in close collaboration with BU SVPs, VPs, and their leadership teams to develop and lead the vision, strategy, and execution for field-facing colleague engagement and operations—enabling exceptional colleague and customer experiences.</p><p>This individual will be responsible for significantly elevating the enablement of customer-facing teams by architecting scalable field excellence capabilities, modernizing field engagement models, and institutionalizing the behavioral change necessary to optimize field performance and commercial outcomes.</p><p>This leader will serve as the primary architect of Regeneron field excellence strategy, working closely with business unit commercial and field leaders to ensure that capability investments and engagement programs are tightly aligned with business priorities. Responsibilities extend to designing and overseeing the institution of new programs, operationalizing ways of working across field and cross-functional teams, and embedding the behavior change solutions required to ensure transformations are adopted, effectively integrated into workflow, and continuously optimized in service of the business.</p><h3>When & where:</h3><ul><li>In the office located in Sleepy Hollow, NY for 4 days a week</li></ul><br><h3>Discover your role:</h3><p><strong>Field Excellence Strategy & Vision</strong></p><ul><li>Define and communicate the long-term vision for Regeneron field enablement and engagement strategy across business units, ensuring alignment with each BU’s commercial priorities and organizational goals.</li><li>Develop a holistic strategy for how field-facing colleagues engage customers—HCPs, institutions, and payers—and how the organization supports them through tools, training, CRM, analytics, and processes.</li><li>Translate vision into a prioritized, multi-year roadmap outlining capabilities, tools, processes, engagement models, and metrics to build and optimize over a 1–3 year horizon.</li></ul><h3><strong>Field Enablement & Excellence</strong></h3><ul><li>Lead field enablement initiatives for all customer-facing colleagues, ensuring they have the tools, processes, intelligence, and support to deliver differentiated, high-impact customer engagements.</li><li>Partner closely with training teams to design and implement role-specific programs that build field capability, ensure effective adoption of new tools and workflows, and maintain launch readiness.</li><li>Define metrics and success criteria for all field enablement programs; oversee and monitor performance against these standards with rigor and transparency.</li></ul><p><strong>Field Excellence Lead Team Coordination</strong></p><ul><li>Provide strategic leadership and direction for cross Portfolio initiatives to a Field Force Effectiveness colleagues who are embedded within and report into the individual business units—functioning as a cohesive, enterprise-wide field excellence capability without formal direct management authority.</li><li>Establish clear operating rhythms, performance standards, and cross-BU coordination mechanisms to ensure Field Excellence Leads operate with consistency, alignment, and shared accountability for commercial outcomes.</li><li>Develop and socialize common frameworks, toolkits, and playbooks that Field Excellence Leads can adapt and deploy within their respective business units.</li></ul><p><strong>Engagement Strategy</strong></p><ul><li>Codify role scope, remits, and ways of working across functions and business units (xRole and xBU), ensuring alignment and consistency in engagement approaches where appropriate.</li><li>Design holistic, cross-functional engagement solutions that leverage the full customer-facing team—Sales, Medical Affairs, Market Access, and Account Management—to deliver seamless, high-value customer experiences.</li><li>Support the voice of the customer within the organization, ensuring that HCP, institution, payer, and account needs are understood and translated into meaningful, consistent, high-quality engagements.</li></ul><p><strong>Commercial Technology & Digital Enablement</strong></p><ul><li>Lead the implementation and integration of CRM technology to support pre-call planning, next-best-action recommendations, and field productivity—ensuring seamless integration into daily workflows.</li><li>Oversee field enablement for AI-driven solutions that enhance customer engagement, improve field productivity, and deliver actionable insights in real time.</li><li>Collaborate with IT, SI&A, and Commercial Operations teams to integrate tools and technologies into field workflows without disruption to ongoing commercial activity.</li></ul><p><strong>Cross-Functional Leadership & Execution</strong></p><ul><li>Act as a senior partner across the business, collaborating with leaders in Marketing, Sales, Medical Affairs, Market Access, Commercial Operations, Compliance, IT/Analytics, and Training to ensure alignment of en</li><li>Govern relevant technology and analytics investment priorities as a cross-functional partner, ensuring MarTech, CRM, and digital engagement platforms are tightly aligned with business priorities and deliver measurable commercial outcomes.</li><li>Represent field excellence priorities on senior leadership forums, governance councils, and cross-functional investment committees to ensure field enablement is treated as a strategic commercial driver.</li></ul><h3>This role requires:</h3><ul><li>At least 14 years of progressive experience in the pharmaceutical or biotech industry, with significant leadership experience in commercial operations, field excellence, field enablement, or analogous commercial enablement roles.</li><li>Deep, hands-on experience designing and deploying field enablement frameworks, including Next Best Action (NBA), CRM optimization, and AI-driven insight tools within a pharmaceutical or life sciences commercial organization.</li><li>Proven track record of leading large-scale commercial transformations—including organizational design, operating model redesign, and capability scale-ups across field organizations of 500+ personnel.</li><li>Demonstrated success managing complex, matrixed environments with influence across senior leadership, cross-functional partners, and distributed field teams without formal direct authority over all resources.</li><li>Experience designing and executing behavior change and adoption programs that successfully embed new tools, processes, and ways of working into field workflows.</li><li>Background in field deployment, incentive design, field force effectiveness (FFE), field analytics, and virtual engagement model design preferred.</li><li>Experience with account management frameworks, IDN/organized customer strategies, and cross-functional engagement models spanning Sales, Medical Affairs, and Market Access is a strong differentiator.</li><li>Prior experience supporting high-profile product launches, including organizational readiness, field deployment, and engagement model design, strongly preferred.</li><li>Experience as a strategic advisor or internal consultant to senior executive leadership, translating complex business challenges into actionable commercial roadmaps, is highly valued.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Patient Advocacy]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48219]]></requisitionid>
    <referencenumber><![CDATA[R48219]]></referencenumber>
    <apijobid><![CDATA[r48219]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48219/senior-manager-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Patient Advocacy is a strategic and execution-focused role responsible for building trusted relationships with patient advocacy organizations, elevating the patient voice, and delivering compliant, high-impact programs that advance disease education, access, and outcomes. This role partners closely with Medical Affairs, Clinical Development, Market Access, Corporate/External Affairs, and Commercial to ensure patient insights inform decisions from early development through commercialization, and represents the company at patient events, advisory boards, and key congresses.</p><p><strong>Location and Work Model:</strong><br>This role is based in Sleep Hollow, NY, on-site 4 days/week. Travel approximately 25–50% for patient engagements, conferences, and advocacy meetings; some evenings/weekends may be required based on community schedules </p><p><strong>Discover Your Role:</strong></p><ul><li>With Patient Advocacy leadership, lead execution of therapeutically aligned patient advocacy strategy in assigned therapeutic areas.</li><li>Apply and adapt standard methodologies and governance frameworks for engagement with advocacy and professional societies. Identify opportunities to enhance processes and ensure alignment with evolving business needs</li><li>Collaborate with cross-functional partners in Medical, Commercial, Market Access, Policy, and Clinical Development to support established advocacy strategy</li><li>Accountable for delivering measurable improvements in disease awareness, time to diagnosis, clinical trial awareness, access, and patient experience</li></ul><p><strong>Advocacy Strategy and Execution</strong></p><ul><li>Assess shifting company priorities and external dynamics to inform strategic decisions, recommending strategic choices and trade-offs with clear implications for patients and the business</li><li>Continuously evolve therapeutic area advocacy strategies and operating plans, including educational programs, disease awareness, advisory boards, patient speaker engagement, clinical trial awareness, and coordination on relevant policy initiatives</li><li>With Patient Advocacy leadership, lead the development and execution of advocacy campaigns; ensure external partner plans align to Regeneron’s goals and compliance standards</li><li>Coordinate and design patient advisory boards and insight-generation activities, ensuring strategic alignment, high-quality outputs, and effective dissemination of insights to inform decision-making. Ensure materials developed for ad boards are accurate, inclusive, and compliant.</li></ul><p><strong>Executive Engagement and Influence</strong></p><ul><li>Serve as a trusted advisor to leaders; create materials/presentations that articulate patient impact, risks, and demonstrate Patient Advocacy’s role in supporting Regeneron’s business objectives</li><li>Represent the company at advocacy meetings, conferences, and coalition activities; identify collaboration opportunities and areas of mutual interest </li><li>Monitor policy and access topics impacting patient communities and partner with internal stakeholders on advocacy positions and engagement plans </li></ul><p><strong>Relationship Management</strong></p><ul><li>Build and maintain long-term, trust-based partnerships with patient advocacy and professional societies at national and regional levels; serve as a responsive, empathetic point of contact </li><li>Ensure Regeneron’s leadership position is evident through presence at priority events; synthesize and disseminate insights to internal stakeholders</li></ul><p><strong>Cross-Functional Collaboration and Alignment</strong></p><ul><li>Build strong, collaborative relationships with Medical, Commercial/Brand, Market Access, Government Affairs, Health Policy, Clinical Development, and Legal/Compliance</li><li>Drive cross-functional alignment and execution of advocacy initiatives; co-create plans with Alliance partners where applicable</li><li>Contribute to therapeutically aligned assigned strategy and annual planning and budgeting.</li></ul><p> <strong>Patient Voice and Insights</strong></p><ul><li>Lead initiatives that elevate patient voice, such as advisory boards, listening sessions, and patient storytelling, ensuring insights inform clinical development and commercialization plans </li><li> Champion a patient-centric mindset and provide the patient perspectives to inform clinical trial design, evidence generation, disease education, patient services, and access strategies</li></ul><p><strong>Financial and Business Acumen</strong></p><ul><li>Track engagement metrics, manage budgets, and report outcomes to leadership </li></ul><p><strong>Grants and Governance </strong></p><ul><li>Strategically fund programs that advance patient engagement and disease education aligned to therapeutic priorities Act as a grant reviewer as part of a compliant grant review process; manage budgets and financial stewardship effectively and in a timely manner Ensure all interactions adhere to legal, regulatory, and compliance standards; maintain high transparency and trust with stakeholders </li></ul><p><strong>This Role Requires:</strong></p><ul><li>Bachelor’s degree required; advanced degree a plus (e.g., MPH, MS, MA in Communications/Health Policy).</li><li>8+ years of industry experience, patient advocacy, community engagement, or related roles within biopharma/biotech or patient organizations</li><li>Experience building high-trust partnerships with diverse stakeholders, stakeholder management; proven ability to translate insights into action </li><li>Strong project management skills with experience executing multi-stakeholder programs and events on time and within budget.</li><li>Excellent communication skills (written, verbal, and presentation) with executive presence.</li><li>Working knowledge of clinical development, real-world evidence, market access, and the compliance environment for patient interactions (e.g., sponsorships, fair market value, privacy, AE reporting).</li><li>Comfortable operating in a matrixed, fast-paced environment with shifting priorities.<strong> </strong></li></ul><p><strong>Preferred</strong></p><ul><li>Experience in rare diseases, oncology, hematology, and/or cardio-metabolic<strong> </strong></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Validation Specialist, Fill Finish]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46783]]></requisitionid>
    <referencenumber><![CDATA[R46783]]></referencenumber>
    <apijobid><![CDATA[r46783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46783/principal-qa-validation-specialist-fill-finish/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Quality Assurance (QA) Validation Specialist to join our QA Validation team. They will lead the utilities and EMPQ team for our internal fill finish facility, overseeing qualification of utilities, cleanrooms, and filling lines critical to commercial production; ensure regulatory compliance, strengthen the contamination control strategy, and drive key licensure activities.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead validation and serve as SME for utilities and environmental qualification; assess change controls, review CAPAs/NOEs, approve documents, and lead audits</li><li>Plan and execute cleanroom qualifications and requalification; oversee EMPQ for filling line clean air equipment</li><li>Drive QRM deliverables including HACCP assessments and continuous trending/reporting</li><li>Lead investigations of contamination events associated with environmental monitoring in cleanrooms and clean air equipment</li><li>Qualify critical utilities: Water for Injection (WFI) , pharmaceutical air, AHUs, clean steam generators, and nitrogen distribution systems</li><li>Manage and develop a specialist and a team of consultants to meet project milestones and deliver qualification/documentation deliverables</li><li>Establish processes that ensure compliance with regulatory requirements, including participation in Annex 1 gap assessments</li><li>Influence the creation and revision of local/global policies, standards, procedures, and business processes to align with industry best practices</li><li>Demonstrated experience in a cGMP-regulated environment, including validation, inspection and audit readiness</li><li>Possesses strong cross-functional collaboration and communication skills</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Engineering, Chemistry, or Life Sciences and 8+ years of relevant experience</li><li>Experience in utility and facility qualification/validation</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Information Security Analyst - Insider Risk]]></title>
    <date><![CDATA[Wed, 22 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49245]]></requisitionid>
    <referencenumber><![CDATA[R49245]]></referencenumber>
    <apijobid><![CDATA[r49245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49245/sr-information-security-analyst-insider-risk/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Job Description</p></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p><p>The Insider Risk Analyst supports Regeneron's insider risk capability within the Global Data Protection & AI Security pillar, working alongside the Insider Risk & IP Protection lead. The role focuses on insider data risk, intellectual property protection, and employee-risk procedures, applying detection, triage, and case-management skills with discretion and defensible casework. Reporting lines in the pillar stay flat to the Senior Director; the analyst partners closely with HR, Legal, and the Data Protection Monitoring function on insider signal. </p></div></div></div></div></div></div></div></div></div><p><strong>Where: </strong>Based at our Sleepy Hollow, NY location</p><p><strong>When: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Support the insider risk program: detection, triage, and case management for insider data risk. </p></li></ul><ul><li><p>Contribute to IP-protection monitoring across sensitive data and research assets. </p></li></ul><ul><li><p>Support employee-risk procedures, including performance-plan-related monitoring, in partnership with HR and Legal. </p></li></ul><ul><li><p>Partner with the Data Protection Monitoring and Engineering functions on insider signal quality and tuning. </p></li></ul><ul><li><p>Maintain case documentation and chain-of-custody discipline. </p></li></ul><ul><li><p>Support investigations and escalations with appropriate confidentiality and legal coordination. </p></li></ul><ul><li><p>Apply insider-risk detection use cases and thresholds, escalating material findings to the Insider Risk & IP Protection lead. </p></li></ul><ul><li><p>Contribute to insider-risk reporting and metrics for pillar leadership.</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>Bachelor's degree in Information Technology, Computer Science, Cybersecurity, Criminal Justice, or related field required. </p></li><li><p>4+ years in security, insider risk, or investigations. </p></li><li><p>Experience supporting insider-risk or DLP investigations with HR/Legal partnerships.</p></li></ul><ul><li><p>Case management and documentation discipline, including chain of custody. </p></li></ul><ul><li><p>Familiarity with insider-risk detection signal and behavioral indicators. </p></li></ul><ul><li><p>Working knowledge of data protection concepts and how monitoring signal supports insider cases.</p></li></ul><p>Preferred</p><ul><li><p>Insider-risk tooling experience (e.g., DLP, UEBA, insider-risk platforms). </p></li></ul><ul><li><p>Investigations or e-discovery background. </p></li></ul><ul><li><p>Regulated industry experience. </p></li></ul><ul><li><p>Relevant certifications (e.g., Security+, CFE, or equivalent). </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY -  ATLANTA SOUTH, GA]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48920]]></requisitionid>
    <referencenumber><![CDATA[R48920]]></referencenumber>
    <apijobid><![CDATA[r48920]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48920/medical-account-specialist-ii-hematology-atlanta-south-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Atlanta - South, GA</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Health Economics & Outcomes Research, Solid Tumors]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45357]]></requisitionid>
    <referencenumber><![CDATA[R45357]]></referencenumber>
    <apijobid><![CDATA[r45357]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45357/associate-director-health-economics-outcomes-research-solid-tumors/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. As an Associate Director you will develop HEOR strategies and plans, conduct HEOR and RWE studies and develop publications and deliverables. We work closely with Market Access, Medical Affairs, Clinical Development, Commercial, Regulatory and other groups to ensure evidence needs are identified and addressed to demonstrate the value with a focus on solid tumors<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Sleepy Hollow, NY</p><p><strong>Discover your role:</strong><br>• Develop and implement HEOR strategies and programs throughout the product’s lifecycle, to inform and support clinical development and regulatory needs during early pipeline phase and ensuring optimal market access.<br>• Collaborate with business partners to develop and support compelling product value propositions with aim to optimize patient access.<br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation.<br>• Leverage RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams generating insights to inform development programs and key business questions.<br>• Co-lead conduct of regulatory-grade real world evidence studies and provide education on emerging opportunities for employing RWE across the solid tumor portfolio.<br>• Collaborate on conduct and communication of epidemiology and pharmacoepidemiology analyses and studies.<br>• Provide relevant input into selection of patient population, comparators and endpoints within clinical trials to enable demonstration of robust incremental value over standard of care that can facilitate optimal patient access.<br>• Develop and implement Clinical Outcomes Assessment (COA) measurement strategies and plans in support of product labeling, patient access and product differentiation.<br>• Develop and validate COA endpoints for integration in clinical studies. Produce COA evidence dossiers for regulatory submissions.<br>• Evaluate relevant payer and health technology assessment (HTA) decisions, collect feedback in advisory meetings and apply key takeaways. <br>• Maintain an up-to-date awareness of regulatory and payer/HTA considerations that may impact planning for and implementation of HEOR programs.<br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.</p><p><strong>This role requires:</strong><br>• An Advanced degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field and 4+ years with PhD or 6+ years with MS in HEOR; at least 3 years of life science company or healthcare consulting experience is a plus. <br>• Strong technical expertise required in design and conduct of HEOR studies and models. <br>• Solid understanding of regulatory (e.g. FDA, EMA) and HTA considerations. <br>• Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data. <br>• Experience with Oncology is preferred<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician (Overnights)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49735]]></requisitionid>
    <referencenumber><![CDATA[R49735]]></referencenumber>
    <apijobid><![CDATA[r49735]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49735/calibration-technician-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking to add a Calibration Technician to our growing team. Calibration Technicians support our manufacturing operations by performing mechanical, electrical, calibration, electronic, and utility-related tasks. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: East Greenbush, NY</li><li>Working shift: Monday-Friday 10:00pm-6:30am</li><li>Training shift: Monday-Friday 8:00am-4:30pm for approximately 6 months</li></ul><br><h3>Discover your role:</h3><ul><li>Calibrate various types of instrumentation including temperature, pressure, level, flow, and analytical instruments</li><li>Perform loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Work with medium and low voltages</li><li>Perform basic plumbing and tube bending jobs</li><li>Assist the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Perform daily Work Orders (WO) and Preventative Maintenance (PM), and efficiently coordinating the workflow and documentation of PMs and WOs</li><li>Communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work, as needed</li><li>Participate in compliance investigations if and when necessary</li></ul><br><h3>This role requires:</h3><ul><li>AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum years of related experience: 2+ years or HSD/GED and 5+ years for Calibration Technician II, 5+ years or HSD/GED and 8+ years for Calibration Technician III, 8+ years or HSD/GED and 11+ years for Calibration Technician IV</li><li>Demonstrated basic problem-solving skills</li><li>Ability to learn and follow routine procedures independently as well as part of a team</li><li>The ability to lift, push, and pull at least 50 lbs</li><li>Participating in a rotating on-call schedule</li><li>Strong written and verbal communication skills</li><li>Ability to maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><br><h3><strong>Gowning and Environment:</strong></h3><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Product & Pipeline Communications - Oncology & Hematology]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47986]]></requisitionid>
    <referencenumber><![CDATA[R47986]]></referencenumber>
    <apijobid><![CDATA[r47986]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47986/senior-manager-product-pipeline-communications-oncology-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>BUILD OUR FUTURE TOGETHER:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Corporate Communication to join our Product and Pipeline Communications team within Corporate Affairs, supporting our U.S. and international oncology business in a hybrid role. In this role, you will lead communications for our blood cancer portfolio and pipeline and support solid tumour programmes while collaborating with Commercial, Clinical, Medical Affairs, Legal, Regulatory, and in-country Corporate Affairs teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>WHEN & WHERE: </strong>Sleepy Hollow, NY. Hybrid, minimum four days on-site per week.</p><p><br><strong>DISCOVER YOUR ROLE:</strong><br>- Lead U.S. and Global communications for our blood cancer portfolio and pipeline</p><p>- Partner with Commercial, Clinical, Legal, and Regulatory teams as a trusted strategist and media coach</p><p>- Manage media relations, congress support, regulatory milestones, and stakeholder engagement</p><p>- You translate complex science into compelling narratives for diverse external audiences</p><p>- Identify and assess communications risks, recommending response strategies</p><p>- Collaborate with in-country Corporate Affairs teams to extend global strategies locally</p><p>- Oversee agency partners, resources, and budget to deliver cohesive outcomes</p><p>- You build consensus and foster trusted relationships across functions and levels</p><p><br><strong>THIS ROLE REQUIRES:</strong><br>- Bachelor's degree with 8–10+ years of relevant experience, including 5+ years in product or pipeline communications (in-house or agency)</p><p>- Strong writing, editing, and content design skills with ability to translate complex clinical data for external audiences</p><p>- Knowledge of the regulatory, commercial, and legal landscape governing pre-approval and post-approval pharmaceutical communications</p><p>- Proven experience with social media and digital communications strategies</p><p>- Experience managing agency partners and vendor workstreams</p><p>- Background in biotechnology or pharmaceutical communications in oncology (preferred)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Sud (Ematologia)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49793]]></requisitionid>
    <referencenumber><![CDATA[R49793]]></referencenumber>
    <apijobid><![CDATA[r49793]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49793/key-account-manager-sud-ematologia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Costruiamo insieme il nostro futuro:</strong></p><p>In Regeneron utilizziamo la scienza e l’innovazione per sviluppare farmaci che cambiano la vita delle persone con malattie gravi. Cerchiamo un Senior Sales Specialist, Ematologia Commerciale, Italia da inserire nel nostro team vendite di ematologia. La posizione supporterà il business italiano con un modello di lavoro sul territorio. In questo ruolo, promuoverai la crescita del territorio e relazioni di valore con i professionisti sanitari. Collaborerai con i colleghi dell’area medica e con altre funzioni. Questa posizione offre l’opportunità di contribuire a un’organizzazione in rapida crescita, guidata dalla scienza e orientata ai pazienti.</p><p><strong>Quando e dove:</strong></p><p>Italia Sud<br>Posizione sul territorio, con trasferte frequenti.</p><p><strong>Scopri il tuo ruolo:</strong></p><ul><li><p>Costruire relazioni di qualità con i professionisti sanitari utilizzando conoscenze scientifiche aggiornate e messaggi di vendita approvati.</p></li><li><p>Attuare i piani commerciali e di marketing per raggiungere gli obiettivi di vendita e gli indicatori di performance.</p></li><li><p>Gestire gli account strategici attraverso pianificazione, targeting e segmentazione, in linea con le indicazioni regionali.</p></li><li><p>Sviluppare piani locali per gli account utilizzando dati di mercato e aggiornarli in base alle dinamiche del mercato.</p></li><li><p>Collaborare con i colleghi dell’area medica su programmi regionali a supporto delle esigenze dei professionisti sanitari.</p></li><li><p>Rappresentare Regeneron Ematologia in congressi e incontri regionali, nazionali e internazionali.</p></li><li><p>Utilizzerai canali diretti e digitali per ottimizzare il coinvolgimento e contribuire al miglioramento della pratica clinica.</p></li></ul><p><strong>Questo ruolo richiede:</strong></p><ul><li><p>Laurea o qualifica equivalente riconosciuta per i professionisti delle vendite.</p></li><li><p>Almeno cinque anni di esperienza nelle vendite farmaceutiche, inclusa un’esperienza essenziale in ematologia.</p></li><li><p>Conoscenza del Codice della Federazione Europea delle Industrie e Associazioni Farmaceutiche e delle normative locali applicabili.</p></li><li><p>Ottima conoscenza dell’italiano; la conoscenza dell’inglese costituisce un vantaggio.</p></li><li><p>Attitudine tecnica alla vendita basata sulla patologia e sui concetti scientifici.</p></li><li><p>Capacità di utilizzare dati, sistemi multipli e piattaforme di Customer Relationship Management.</p></li><li><p>Eccellenti capacità di coinvolgimento del cliente, presentazione, pianificazione e definizione delle priorità.</p></li><li><p>Capacità di lavorare autonomamente entro scadenze ristrette, dimostrando integrità e una comunicazione etica.</p></li><li><p>L’esperienza nel lancio di prodotti costituisce un vantaggio.</p></li></ul><p><strong>Salary Range (annually)</strong></p><p> € 59.325 - € 98.875</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Respiratory *Tokyo, Chiba Area]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49804]]></requisitionid>
    <referencenumber><![CDATA[R49804]]></referencenumber>
    <apijobid><![CDATA[r49804]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49804/medical-representative-mr-respiratory-startokyo-chiba-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Sales Representative Immunology Dermatology Japan to join our Immunology Commercial Team, supporting our Japan business in a field-based work mode. In this role, you will achieve dermatology sales objectives through strategic territory management while collaborating with alliance partners and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Japan</p><p>Work model: Field-based</p><br><p><strong>Discover your role:</strong></p><ul><li>Achieve respiratory sales objectives through effective territory and budget management.</li><li>Develop annual territory business plans using market insights and brand strategies.</li><li>Create territory action plans using key data sources.</li><li>Deliver customer value through disease and concept-focused selling.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Ensure compliance with Regeneron legal and regulatory requirements.</li><li>Collaborate with alliance partners to achieve shared business objectives.</li><li>You build trusted customer relationships and adapt to changing market needs.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree or equivalent.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Valid driver license and MR Certification.</li><li>Strong customer engagement skills with a focus on value delivery.</li><li>Ability to conduct disease and concept selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and territory management capabilities.</li><li>Ability to present effectively to diverse audiences.</li><li>Ability to work independently against strategic and tactical plans.</li><li>Computer proficiency with word processing, spreadsheets, databases, and email software.</li><li>Alliance partnership experience.</li><li>Therapy area knowledge in respiratory or ENT and biologics sales experience preferred.</li><li>Current clinical knowledge of relevant therapy areas and competitor products preferred.</li><li>Established Key Opinion Leader relationships within respiratory or ENT preferred.</li><li>English fluency is a plus.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations, Infrastructure Architecture]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45562]]></requisitionid>
    <referencenumber><![CDATA[R45562]]></referencenumber>
    <apijobid><![CDATA[r45562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45562/associate-director-of-it-operations-infrastructure-architecture/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Infrastructure Architecture Leader (Senior Manager or Associate Director) to join our IOPS IT team, ensuring the reliable operation and strategic development of IT and Operational Technology infrastructure across our GxP manufacturing environment. In this role, you will define and lead infrastructure architecture — spanning hyper-converged systems, advanced networking, and wireless technologies — while collaborating with corporate IT, automation teams, service providers, and cross-functional partners to maintain secure, scalable, and compliant operations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am -4:30pm</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Define, implement, and lead IT/OT infrastructure architecture with a focus on hyper-converged systems, advanced networking, and wireless technologies; design and document infrastructure architecture across networking, compute, and security domains</li><li>Ensure reliable operation of IT/OT infrastructure including servers, hardware, communications, and desktop support; provide operational oversight for data centre operations, network services, telecom, and asset management</li><li>Build scalable and secure wireless networks to support industrial and enterprise needs; maintain robust security measures including data integrity and disaster recovery planning</li><li>Apply security frameworks such as NIST CSF, IEC 62443, or ISO 27001 within a regulated environment; maintain compliance with automation system standards including DeltaV/Emerson and Rockwell/Allen-Bradley</li><li>Ensure compliance with GxP, FDA, and global regulatory requirements; ensure systems and procedures support effective monitoring, reporting, and audit readiness</li><li>Manage service providers to ensure high-quality delivery aligned to SLAs; act as escalation point for major incidents and provide regular management reporting on service performance and IT operations</li><li>Collaborate with corporate IT and OT partners to ensure seamless system integration and alignment across the enterprise</li><li>Lead, mentor, and develop a diverse technical team spanning Helpdesk, Desktop, Server, and Network functions; oversee recruitment, training, performance evaluations, and goal setting for the IT Operations team</li><li>Hands-on experience designing and documenting infrastructure architecture across networking, compute, and security domains required</li><li>Demonstrated experience with security frameworks such as NIST CSF, IEC 62443, or ISO 27001 and applying them within regulated environments</li><li>Demonstrated experience managing diverse technical teams including Helpdesk, Desktop, Server, and Network staff; experience managing vendors and managed service providers required</li><li>Experience developing and deploying SLAs, metrics, and operational best practices; proven track record implementing ITIL practices within an organization</li><li>Strong background in Microsoft OS including Server and GPO elements; strong understanding of data integrity and associated tools</li><li>Experience with Business Continuity and Disaster Recovery planning required</li><li>Knowledge of IT compliance guidelines including PIC/S, 21 CFR Part 11, Annex 11, and GAMP preferred</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>BS/BA in Information Technology or a related field</li><li>Senior Manager: 8+ years of progressively more responsible experience, including 8+ years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment</li><li>Associate Director: 10 years of progressively more responsible experience, including 10 years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Trademark and Copyright Attorney]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49506]]></requisitionid>
    <referencenumber><![CDATA[R49506]]></referencenumber>
    <apijobid><![CDATA[r49506]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49506/director-trademark-and-copyright-attorney/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We are seeking a Trademark Attorney to join our in-house legal team, supporting the global trademark portfolio for our pharmaceutical products and corporate brands. This role is ideal for an attorney with a strong foundation in trademark prosecution and brand protection who is looking to deepen their expertise in the highly regulated, high-stakes environment of pharmaceutical branding — where trademark strategy intersects closely with regulatory approval (Food and Drug Administration, European Medicines Agency, and other health authorities), risk management, and commercial strategy.</p><div><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><ul><li><p>Manage the global trademark portfolio (prosecution, maintenance, renewals, and enforcement) for prescription product brands, corporate names, and pipeline candidates</p></li><li><p>Supervise outside counsel in preparing and prosecuting global trademark applications relating to commercial and patient/educational activities</p></li><li><p>Conduct and oversee trademark clearance searches and provide advice to internal clients on third-party trademarks and freedom-to-operate risk</p></li><li><p>Support legal clearance for secondary nomenclature needs such as INNs, logo designs, foreign language transliterations, and 4-letter biologic suffixes for new product compounds, line extensions, in-licensed and co-marketed drugs, devices, digital apps, and patient support programs</p></li><li><p>Advise commercial, marketing, and branding teams on trademark selection, usage guidelines, and brand protection strategy across all channels (packaging, promotional materials, digital/social media)</p></li><li><p>Draft and negotiate trademark-related agreements, including licensing, coexistence, consent, and settlement agreements</p></li><li><p>Manage domestic and international trademark filings and prosecution through outside counsel networks; oversee budgets and vendor relationships</p></li><li><p>Manage enforcement actions against third parties seeking to misappropriate company names, products, websites, and internet domain names, including UDRP proceedings; monitor the marketplace and online channels for infringement, counterfeiting, and grey-market issues; handle opposition/cancellation proceedings before the USPTO/TTAB and foreign trademark offices</p></li><li><p>Support counterfeiting mitigation by registering trademarks with U.S. Customs and Border Protection (CBP) and equivalent global agencies, and partner with Corporate Security, Communications, Commercial, and Digital teams to address cybersquatting and online brand misuse</p></li><li><p>Coordinate with in-house litigation colleagues on trademark infringement, unfair competition, and related disputes in federal and state court, including case strategy, discovery support, and expert coordination</p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>J.D. from an accredited law school and active bar membership in good standing (state bar as applicable)</p></li><li><p>5 plus years of trademark law experience, with a mix of law firm and/or in-house experience preferred</p></li><li><p>Substantive experience with trademark prosecution, portfolio management, and enforcement</p></li><li><p>Experience in the pharmaceutical, life sciences, or healthcare industry strongly preferred; familiarity with FDA proprietary name review process a plus</p></li><li><p>Experience with international trademark filing strategy and coordination with foreign counsel</p></li><li><p>Strong drafting and negotiation skills, including licensing and coexistence agreements</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43877]]></requisitionid>
    <referencenumber><![CDATA[R43877]]></referencenumber>
    <apijobid><![CDATA[r43877]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43877/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming team, supporting a therapeutic area across our clinical portfolio. In this role, you will provide programming leadership on project teams, overseeing deliverables from single studies through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and departmental colleagues to shape and implement programming standards.</p><h3>When & where:</h3><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: onsite</li></ul><h3>Discover your role:</h3><ul><li>Coordinate and oversee analysis programming within your therapeutic area, tracking progress and completion of deliverables</li><li>Manage and coordinate programming and quality control of analysis datasets and outputs in support of regulatory submissions</li><li>Mentor others on the use of standardization tools and therapeutic area standard analysis approaches</li><li>Serve as the programming representative on a multidisciplinary study team, ensuring timely, quality support through regulatory approval and launch</li><li>Develop data models, programming standards, and code, and train end users on project standards</li><li>Mentor junior staff, fostering a collaborative environment and modeling strong team behavior</li><li>Contribute to programming development and quality control using established tools and methodologies</li><li>Advise team members on procedures for data, records, and information retention</li></ul><h3><strong>This role might be for you if you:</strong></h3><ul><li>Enjoy leading programming work independently while staying closely connected to a broader project team</li><li>Think in terms of standards, consistency, and reusable processes across studies</li><li>Communicate clearly with cross-functional and multidisciplinary stakeholders</li><li>Take pride in mentoring and developing less experienced colleagues</li><li>Stay organized and detail-oriented when managing multiple deliverables and timelines</li><li>Approach quality control with rigor and a genuine sense of ownership</li><li>Adapt comfortably to shifting priorities, including ad hoc requests from senior leadership</li></ul><h3>This role requires:</h3><ul><li>Master's degree with 8-10 years of relevant experience</li><li>Proven experience leading programming deliverables within a clinical or therapeutic area</li><li>Strong mentoring and team collaboration skills</li><li>Experience developing and applying programming standards and data models</li></ul><h3><strong>Nice to haves:</strong></h3><ul><li>SAS Certification</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Clinical Data Management]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45840]]></requisitionid>
    <referencenumber><![CDATA[R45840]]></referencenumber>
    <apijobid><![CDATA[r45840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45840/senior-director-clinical-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3>Build our future together</h3><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Clinical Data Management, India to join our Clinical Data Management Leadership Team, supporting our clinical pipeline in an on-site role. You will shape the global operational vision and strategy for Data Management, build a high-performing regional organisation, and support the recruitment of top talent across other R&D functions. You will also act as the local R&D Lead for the Global Capability Centre, working across Clinical Data Operations, Central Services, External Data Acquisition, and external partners.</p><br><h3>When & where</h3><p>Hyderabad (on-site).</p><br><h3>Discover your role</h3><ul><li><p>Build and lead a regional Clinical Data Management organisation spanning reporting, review, coding, laboratory data processing, and database operations.</p></li><li><p>Serve as the R&D Lead for the Regeneron Global Capability Centre and the local point of contact for all R&D functions.</p></li><li><p>Provide local leadership and guidance while supporting culture and engagement across R&D teams.</p></li><li><p>Define functional metrics and quality indicators to drive compliance, quality, and timely portfolio delivery.</p></li><li><p>Oversee functional service providers and external data vendors, managing performance and risk.</p></li><li><p>Lead cross-functional initiatives that strengthen operations, improve efficiency, and support inspection readiness.</p></li><li><p>Advance automation and AI solutions that reduce manual effort and accelerate data access.</p></li><li><p>Shape organisation design, evaluate resource needs, and hire and develop talent across the team.</p></li></ul><h3>This role requires</h3><ul><li><p>15+ years of clinical data management experience in pharmaceutical or biotech, including 10+ years of functional leadership and 8+ years of people management.</p></li><li><p>Experience leading teams of 50–150 supporting global data management functions.</p></li><li><p>Strong knowledge of clinical data management regulations and standards, including 21 CFR Part 11, ICH-GCP, GxP, and GDPR.</p></li><li><p>Expertise in clinical data management systems such as EDC, eSource, eCOA, IRT, and medical coding platforms.</p></li><li><p>Willingness to travel up to 25%.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49635]]></requisitionid>
    <referencenumber><![CDATA[R49635]]></referencenumber>
    <apijobid><![CDATA[r49635]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49635/associate-medical-director-clinical-development-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Clinical Development Program (CDP) team, supporting our Ophthalmology therapeutics portfolio. In this role, you will serve as Medical Lead for clinical trials, designing clinical study concepts and leading the Global Clinical Study Team, while collaborating with discovery teams, the Therapeutic Head, and Strategic Program Teams to deliver high-quality, scientifically sound program milestones. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY or Cambridge, MA</p></li><li><p><strong>Travel: </strong>10% to relevant conferences</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Act as medical expert and leader in interactions with external stakeholders</p></li><li><p>Define clinical trial-related Clinical Development Program goals and objectives</p></li><li><p>Partner with discovery teams to shape the next generation of targets in the field</p></li><li><p>Ensure the scientific accuracy of clinical study concepts through rigorous review and consultation with internal and external experts</p></li><li><p>Present clinical study concepts to the Therapeutic Head, Strategic Program Teams, and internal governance meetings</p></li><li><p>Lead the Global Clinical Study Team to deliver high-quality program milestones on schedule</p></li><li><p>Oversee the medical content of clinical study reports and the analysis of clinical data, including safety monitoring, to ensure patient safety</p></li></ul><br><h3>This role requires:</h3><ul><li><p>MD or equivalent, with board eligibility or certification in Ophthalmology</p></li><li><p>0-2 years of academic clinical or translational research experience</p></li><li><p>Experience in Ophthalmic drug development strongly preferred</p></li></ul><p>#MDJobs, #MDJobsCD, #Ophthalmology, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$243,600.00 - $329,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Imaging]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49800]]></requisitionid>
    <referencenumber><![CDATA[R49800]]></referencenumber>
    <apijobid><![CDATA[r49800]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49800/senior-scientist-imaging/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Scientist, MRI to join our Imaging team. The successful candidate will work with the Imaging team's Lead MRI Scientist to execute preclinical MRI studies of rodent models, in collaboration with various therapeutic focus areas, technology teams, and imaging scientists at Regeneron. This will involve coordinating with scientists on experimental design, planning and scheduling animal imaging sessions, acquiring MR images using the 7T Bruker BioSpin system, and ensuring MRI data are relevant, actionable, and of high quality. These data and derived results will be packaged for communication to Regeneron's broader scientific community. You will also collaborate with imaging and therapeutic focus area scientists to optimize and develop MRI protocols for a variety of new MRI techniques and animal models.</p><p>Current and emerging projects include cardiac imaging of the mouse and rat heart to derive structural and functional endpoints; neuroanatomical volume measurements from high-resolution in vivo brain imaging to measure volumetric brain changes associated with aging and disease; high-resolution anatomical imaging of the inner ear; and magnetic resonance spectroscopy to measure local brain metabolite concentration in genetic models of metabolic disorders. Regeneron's broad biological focus guarantees that you will always have something new to learn and contribute to.</p><p><strong>When & where:</strong></p><p>Location: Tarrytown, NY - On-site</p><p><strong>Discover your role:</strong></p><ul><li><p>Working closely with the lead MRI scientist to understand project needs and priorities, troubleshoot experiments, and provide updates on project progress</p></li><li><p>Independently executing projects planned in consultation with the lead MRI scientist and in collaboration with scientists and specialists in Imaging and relevant therapeutic focus areas</p></li><li><p>Operating and optimizing the high field strength MRI for in vivo and ex vivo studies of preclinical rodent models, including critical evaluation of data acquisition</p></li><li><p>Performing relevant animal handling, such as administration of anesthesia, preparing animals for scanning, administration of contrast agents, animal monitoring, and preparation of tissue for ex vivo imaging</p></li><li><p>Maintaining online and physical records of data from ongoing and completed projects</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An MSc or PhD in Engineering, Biophysics, Biology, Chemistry, or a similar field</p></li><li><p>5+ years of experience operating in vivo rodent MRI, and 5+ years of in vivo mouse/rat handling, including anesthesia, injections, and tissue processing</p></li><li><p>Prior experience with 3D MRI visualization software such as 3D Slicer, ITK Snap, or ImageJ</p></li><li><p>Knowledge of basic MRI science and the ability to communicate it to a general audience</p></li><li><p>Knowledge of mouse and rat anatomy, with the ability to incorporate this into MRI study design</p></li><li><p>Prior experience with Bruker ParaVision software, MRI protocol development, cardiac/respiratory/functional gating or triggering techniques, and MRI/MRS processing software (VivoQuant, Amira, LCModel, FID-A, FSL, etc.) preferred</p></li><li><p>Exceptional critical thinking, attention to detail, scientific rigor, and strong analytical, problem-solving, and troubleshooting skills</p></li><li><p>The ability to shift focus between multiple projects while still meeting deadlines</p></li><li><p>A proven ability to work independently and collaboratively as part of a larger project</p></li><li><p>A positive attitude and willingness to learn new things</p></li><li><p>A passion for biology and helping others</p></li><li><p>A dedication to sharing, collaborating, and lifting others up</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Market Access Analytics]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49507]]></requisitionid>
    <referencenumber><![CDATA[R49507]]></referencenumber>
    <apijobid><![CDATA[r49507]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49507/director-market-access-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director </strong>to join our <strong>Market Access Analytics</strong> team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p>The Director, Market Access Analytics will partner with Market Access and the Business Unit, by developing and communicating actionable insights derived from secondary data analytics that effectively shape market access, brand strategy and tactics across different customer segments. This includes developing and implementing the analytics plan, informing business decisions, and designing and implementing analytical solutions to support business opportunities. As part of the role, the Director, Market Access Analytics will develop, build and socialize new analytics capabilities that provide actionable insights based on customer and market understanding. The Director, Market Access Analytics will work with cross-functional business partners to support data-driven decision making, pull through key insights, and build business understanding. In addition to strong analytics skills, the Director, Market Access Analytics should have excellent communication skills, a demonstrated track record of effective business partnership, business impact and influence. This role is hands-on and does not have any direct reports, but will manage contractors, consultants and vendors to complete projects. </p><p><em>Lead & Develop</em></p><ul><li><p>Develop and implement market access analytics plans, and managing the budget</p></li><li><p>Identify business needs and proposing potential market access analytics approaches for solutions. Using business understanding to translate unstructured, complex business problems into the appropriate data problem, models, and analytical solutions</p></li><li><p>Support ongoing and planned contracting strategy analytics (E.g., analog assessment, deal/no deal, post deal analytics, patient flow analytics, simulations, analog analytics, etc.), while maximizing pull-through effectiveness</p></li><li><p>Develop performance reporting strategy, augmenting and streamlining current reporting.</p></li></ul><p><em>Execute</em></p><ul><li><p>Conduct strategic analytics such as archetype (of national and regional payers accounts, IDNs, GPOs, 340B, etc.), payer pathway analytics, account segmentation and targeting, etc.</p></li><li><p>Design and conduct patient affordability analytics, access and reimbursement (E.g., landscape and benchmarking, HUB analytics, co-pay analytics and patient out of pocket sensitivity and modeling, etc.)</p></li><li><p>Diagnose performance and measure impact, based on an understanding of key strategic imperatives, business questions and definition of success</p></li><li><p>Monitor provider account access and conducting payer plan and provider analytics</p></li><li><p>Analyze GPO and account and payer level pull through analytics and opportunity analytics based on access</p></li></ul><p><em>Partnership and collaboration</em></p><ul><li><p>Develop and maintain a mutually beneficial partnership with stakeholders across Market Access Analytics, the Business Unit and Insights & Analytics; strike a balance between project rigor, timelines and ability to influence decisions.</p></li><li><p>Manage analytics suppliers and workbench to design, scope, execute and analyze data in the development of business implications</p></li><li><p>Collaborate on specialty pharmacy analytics</p></li><li><p>Inform data strategy and acquisition</p></li><li><p>Comply with regulatory, security, and privacy requirements as it relates to data assets </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>12+ years of pharmaceutical/biotech commercial experience (or 10+ years for MBA/MS), in roles of increasing accountability; prior experience with market-leading brands required and Insights & Analytics-specific experience is preferred</p></li><li><p>Minimum BS/BA in Business Administration, Statistics, Economics, Mathematics, Business Analytics, Marketing Research, etc.; Advanced degree preferred.</p></li><li><p>Experience working with pharma datasets, including prescription, sales data and claims/patient level data sets inclusive of pharma data sources such as IQVIA, Symphony, etc.</p></li><li><p>Firm understanding of Market Access landscape, customers, and channels; being able to connect the relationships between them and the business</p></li><li><p>U.S. Buy and Bill or Medical Benefit Market Access experience is preferred</p></li><li><p>Technical proficiency and knowledge of U.S. drug reimbursement and access, i.e., coverage, coding and payment is required</p></li><li><p>Knowledge of market access and expertise in market access datasets is preferred</p></li><li><p>Experience working with market access datasets is required (e.g., FIA, LAAD, MMIT, etc. )</p></li><li><p>Experience working with prescription, sales data and claims/patient level data sets inclusive of pharma data sources is required (e.gl, IQVIA, Symphony, etc.)</p></li><li><p>Experience coding in SQL, Python/PySpark, R and/or SAS (BASE, STAT, SQL, Macros) is preferred</p></li><li><p>Experience in data visualization and reporting working with commercial business intelligence tools is required (e.g., PowerBI, Tableau, or similar tools)</p></li><li><p>Advanced proficiency in Excel and PowerPoint is required</p></li><li><p>Proficiency in manipulating and extracting insights from large longitudinal data sources, such as claims and other patient level datasets is required</p></li><li><p>Expertise in managing and analyzing a range of large, secondary transactional databases is required</p></li><li><p>Experience in data mining, descriptive analytics, application of statistical methods, analyses and modeling, predictive modeling, opportunity assessment/quantification and simulation is required</p></li><li><p>Communication and influencing skills, with demonstrated ability to succinctly and effectively present compelling reviews of analyses that integrate insights and business implications/actions to be considered</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Northeast]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47570]]></requisitionid>
    <referencenumber><![CDATA[R47570]]></referencenumber>
    <apijobid><![CDATA[r47570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47570/regional-director-neurology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Northeast Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Northeast (New York, Pennsylvania, Massachusetts, Vermont)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Insights & Analytics - Ophthalmology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48440]]></requisitionid>
    <referencenumber><![CDATA[R48440]]></referencenumber>
    <apijobid><![CDATA[r48440]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48440/executive-director-commercial-insights-analytics-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director </strong>to lead our <strong>Commercial</strong><strong> Insights and Analytics Ophthalmology</strong> team. The Executive Director, Commercial Insights and Analytics (I&A), Ophthalmology, will report directly into the Vice President, Commercial Strategy and Insights & Analytics (CSI&A) within the CSI&A department. This role will lead the I&A team responsible for the Ophthalmology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions across some of Regeneron’s leading brands. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Ophthalmology team in providing business analytics, customer insights and competitive intelligence to deliver rich insights to solve key business problems</p><p>2) Set the strategic I&A direction that aligns with CBU priorities and helps drive launch excellence</p><p>3) Serve as a member of the Ophthalmology CBU Leadership Team, providing I&A expertise</p><p>4) Serve as a member of the CSI&A leadership team to drive cross-commercial innovation and best-in-class delivery</p><p><em>Develop</em></p><p>5) Translate complex analyses into compelling insights and recommendations that will be used to inform business decision-making for senior Regeneron teams, including the CBU, Chief Commercial Officer, Chief Executive Officer and Board of Directors</p><p>6) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent</p><p>7) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform brand differentiation, market growth and business impact; and <strong>b)</strong> consider business potential for pipeline products</p><p><em>Partnership and collaboration</em></p><p>8) Collaborate with the Ophthalmology CBU and other members of senior leadership to contribute to ongoing brand strategies and decisions, including long-term data, analytics and insights roadmap</p><p>9) Develop and maintain a mutually beneficial partnership with CBU stakeholders; ensure insight generation and feedback are embraced; strike a balance between project rigor, timelines and ability to influence decisions</p><p>10) Lead efforts to identify and crystalize insights that inform strategic plans for the Ophthalmology CBU </p><p>11) Work with other CSI&A leads to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analyses, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>12) Proactively communicate with the Ophthalmology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>13) Construct and deliver integrated business reviews, I&A summary overviews with the Ophthalmology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>This role requires:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with buy-and-bill brands in highly competitive markets is required</p></li><li><p>Minimum Bachelor’s degree in data science, public health, statistics, engineering, or a related field (MBA, MPH, MS preferred)</p></li><li><p>Functional expertise in business analytics, customer insights, analog forecast development, market access, and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, customer insights, market access analytics, and competitive intelligence</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution with hands on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li><li><p>Ophthalmology disease category experience is strongly desired</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Business Analyst - Velocigene]]></title>
    <date><![CDATA[Thu, 16 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48356]]></requisitionid>
    <referencenumber><![CDATA[R48356]]></referencenumber>
    <apijobid><![CDATA[r48356]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48356/principal-business-analyst-velocigene/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Principal Business Analyst – Velocigene</strong> </p><p>The Principal Business Analyst Velocigene, will work collaboratively with Research & Preclinical Development scientists, as well as other IT stakeholders, to understand and document scientific lab and data processes, and translate these into requirements for the development of data and technology solutions that support Regeneron’s scientific mission. </p><p>As a Principal Business Analyst, a typical day might include the following: </p><ul><li>Translate business strategies, goals, and objectives into clear requirements; document problem statements with quantifiable business value </li></ul><ul><li>Document “as is” and “to be” business processes; identify, verify, and document functional and non-functional requirements using standard methodologies and tools </li></ul><ul><li>Map information system connections and data flows between systems; identify data elements and provide data mapping and data dictionaries </li></ul><ul><li>Write SQL statements to investigate data; understand data lake principles and different database types </li></ul><ul><li>Maintain and prioritize the backlog of requests; ensure the development team has absolute clarity on requirements; manage business stakeholder expectations </li></ul><ul><li>Work with scientists and laboratory personnel to understand business processes and suggest improvements; partner with research scientists and technical teams to define system goals and requirements </li></ul><ul><li>Pursue data quality issues to root cause; collaborate with business and IT partners to address issues intelligently </li></ul><ul><li>Handle a variety of tasks, effectively solve problems with complex variables, and shift priorities as needed in a fast-paced research environment </li></ul><p>This role might be for you if: </p><ul><li>You are passionate about solving complex, interesting problems in a science-driven environment and have a strong interest in contributing to biological research </li></ul><ul><li>You are proficient at clearly communicating—both verbally and in writing—with members at all levels of the organization, including technical and scientific personnel </li></ul><ul><li>You have the ability to work independently and as part of a team, welcome ideas from partners and stakeholders, and proactively seek to innovate </li></ul><ul><li>You are adaptable and attentive to detail, willing to thrive in a fast-paced, ever-changing environment while measuring the effectiveness of new features analytically </li></ul><p>To be considered for this opportunity, you must have a minimum of a Master’s degree in a life science with experience in computer science or information technology, and 5–8+ years of experience in a research, pharmaceutical, biotechnology, or scientific laboratory environment. </p><p>Previous experience in the biotechnology and/or pharmaceutical industry is required. We need someone who is adept at using a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, data modeling frameworks) in order to perform business analysis, elicit and document requirements, map data flows, and drive data quality improvements in a research-focused environment. Previous experience with biological laboratory techniques, bioinformatics methods, relational database concepts, IT project and software development lifecycle methodologies, and managing or leading software development projects is preferred. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Supply Analyst, Kinaxis Maestro]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43446]]></requisitionid>
    <referencenumber><![CDATA[R43446]]></referencenumber>
    <apijobid><![CDATA[r43446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43446/principal-supply-analyst-kinaxis-maestro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Kinaxis Maestro Solution Author to join our IOPS Supply Chain team, supporting planning and execution across our life sciences operations. In this role, you will design, implement, and optimize solutions on the Kinaxis Maestro platform, enabling smarter campaign management, inventory optimization, and lifecycle planning, while collaborating with operations, logistics, manufacturing, finance, and planning teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide, with room to grow into broader solution architecture responsibility as our platform footprint expands.</p><br><h3>When & where:</h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Design and configure Kinaxis Maestro solutions for campaign management, lifecycle planning, and inventory optimization in a complex, regulated supply chain environment</li><li>Translate business requirements into technical specifications; build custom worksheets, dashboards, templates, algorithms, and scripts to enhance platform functionality</li><li>Integrate Maestro with ERP systems (Oracle preferred) and adjacent supply chain platforms; familiarity with GMP frameworks a plus</li><li>Monitor system performance, resolve data integrity issues, and identify opportunities for continuous improvement</li><li>Maintain documentation for workflows, configurations, and validation activities to support deployment and audit readiness</li><li>Partner cross-functionally with operations, logistics, planning, manufacturing, and finance stakeholders to align solutions with evolving supply chain needs</li><li>Train end-users on Maestro functionality and best practices; provide ongoing support and troubleshooting</li><li>Stay current on Kinaxis Maestro advancements and emerging supply chain trends, proposing solutions to enhance resilience and agility</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree in Supply Chain Management, Industrial Engineering, or a related field</li><li>Senior Supply Analyst: 5+ years experience in supply chain planning solutions, including 3+ years hands-on configuration experience with an advanced planning platform (e.g., Kinaxis RapidResponse/Maestro, o9, Blue Yonder, SAP IBP, OMP, Anaplan)</li><li>Principal Supply Analyst: 8+ years experience in supply chain planning solutions, including 3+ years hands-on configuration experience with an advanced planning platform (e.g., Kinaxis RapidResponse/Maestro, o9, Blue Yonder, SAP IBP, OMP, Anaplan)</li><li>Experience in life sciences, pharma, or another regulated/complex manufacturing environment (medical device, aerospace, specialty chemicals) preferred</li><li>Kinaxis Maestro Author certification, Level 1 or higher, preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Mechanical Engineer]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49590]]></requisitionid>
    <referencenumber><![CDATA[R49590]]></referencenumber>
    <apijobid><![CDATA[r49590]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49590/senior-mechanical-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior Mechanical Engineer </strong>to join our <strong>Site Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Acting as the primary Mechanical Engineering representative within multidisciplinary project teams from concept development through design, construction, commissioning, qualification, and handover</li><li>Coordinating with Process, I&C, Electrical, Maintenance, Operations and Quality groups</li><li>Establishing, maintaining and continuously improving site mechanical specifications, design guidelines, equipment datasheets, piping layouts, P&IDs, utility designs, calculations, equipment evaluations, and vendor submissions</li><li>Supporting contractor management, construction activities, commissioning plans, startup activities, qualification support, and system turnover documentation</li><li>Leading mechanical engineering activities supporting manufacturing, laboratories, clean utilities, process utilities, HVAC systems, building services, and site infrastructure projects</li><li>Providing technical oversight and reviewing of engineering consultants, contractors, and vendor designs</li><li>Participating in and leading design reviews, constructability reviews, risk assessments, HAZOPs, and engineering evaluations</li><li>Evaluating new technologies, equipment upgrades, system expansions, and obsolescence replacement projects</li><li>Supporting the development of project scopes, business cases, budgets, schedules, resource plans, and technical justifications</li><li>Collaborating with Operations, Maintenance, Manufacturing Sciences, Process Engineering, Quality Assurance, Validation, EHS, and Facilities groups</li><li>Mentoring junior engineers and providing technical coaching across the Site Engineering organization</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have excellent technical and analytical skills.</li><li>You are skilled at problem-solving and continuous improvement.</li><li>You possess strong communication and collaboration skills.</li><li>You are adaptable and can work in a fast-paced, regulated environment</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Bachelor’s degree in Mechanical Engineering or related discipline.</li><li>Minimum 8 years of engineering experience with increasing responsibility in mechanical systems, utilities, facilities, or project engineering.</li><li>Demonstrated experience leading mechanical engineering activities for projects within pharmaceutical, biotechnology or other highly regulated industries.</li><li>Strong knowledge of mechanical systems including HVAC, utilities distribution, piping systems, pumps, pressure vessels, clean utilities, and facility infrastructure.</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#LI-Onsite #JOBSIEPR #IRELIM #REGNIRLTO</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Clinical Pharmacologist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49943]]></requisitionid>
    <referencenumber><![CDATA[R49943]]></referencenumber>
    <apijobid><![CDATA[r49943]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49943/senior-clinical-pharmacologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As a<strong> Senior Clinical Pharmacologist </strong>this individual is expected to plan, design, implement and analyze in-vivo and in-vitro pharmacokinetic & pharmacodynamic studies working with Clinical Pharmacology, Quantitative Pharmacology, Pharmacometrics/Pharmacodynamics (PK/PD), Toxicology, Bioanalytical, Therapeutic Focus areas and Clinical Development / Regulatory Affairs teams.</p><p>This individual contributes to the scientific understanding of PK/PD for assigned projects, based on quantitative evaluation of the pharmacokinetic and pharmacodynamic profile for research programs, through the application of state-of-the-art knowledge in pharmacokinetics and pharmacodynamics.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA</p></li><li><p>Work model/flexibility: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Plans, designs, implements and analyzes routine Pharmacometrics (PMx) studies to advance scientific knowledge, in collaboration with other team members.</p></li><li><p>Performs analyses such as compartmental modeling, PopPK, translational modelling, disease modelling, Pop PK/PD, E-R analyses (or work closely with Research Specialist or Pharmacometrics Stats Programming team) to deliver Pharmacometrics results, interpretation and discussion.</p></li><li><p>Collaborates with Scientific Writing (and where appropriate with Pharmacometrics Stats Programming team) to ensure TFLs for Pharmacometrics reports are complete. Works in conjunction with Scientific Writing, Quality Control and QAA (as required) to issue study reports in support of IND/CTA submissions and other regulatory documents.</p></li><li><p>With close supervision from senior Pharmacometrics staff, supports preparation of material to be used in regulatory interactions.</p></li><li><p>Contributes to preparation of Pharmacometrics materials for regulatory background packages, e.g. for pre-IND, EOP2, and pre-BLA meetings.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A PhD in Biology, Pharmacology, Engineering or a Pharmacy (Pharm.D.), Medicine (MD) degree and at least 3+ years of relevant Clinical Pharmacology experience.</p></li><li><p>Are able to serve independently as study Clinical Pharmacology/Quantitative Pharmacology/PPKPD lead for moderately complex</p></li><li><p>Is highly skilled in use of relevant software, including MS-Excel, R, R-Studio, Prism, Phoenix WinNonlin, NLME, STAN and NonMem, working in department computing environment to perform advanced PMx analyses.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Solutions Partner (Scientific Data Product Owner)]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49399]]></requisitionid>
    <referencenumber><![CDATA[R49399]]></referencenumber>
    <apijobid><![CDATA[r49399]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49399/associate-director-solutions-partner-scientific-data-product-owner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are seeking an <strong>Associate Director Solutions Partner </strong>to be a Scientific Data Product Owner and to lead the holistic data strategy for modelling, connecting, and managing Research and preclinical development scientific data in our enterprise data lake. This data originates from our transactional lab informatics systems (e.g., ELN, LIMS, instrument and analytical platforms, registration systems), and our goal is to transform it from siloed transactional records into well-modelled, connected, and reusable data products.</p><p>Sitting at the intersection of science, data engineering, and product management, you will own the vision and roadmap for how scientific data from Research and preclinical development is structured and surfaced within the data lake. You will partner closely with Digital & Technology teams that need connected data products to analyze and report on scientific outcomes, and with data scientists who require curated, connected scientific datasets to power analytics, modelling, and AI initiatives. You will also work hand in hand with data engineering teams to build these connected data products in the lake.</p><p>This is a strategic, cross-functional role for someone who understands both the underlying science and the data architecture required to make that science discoverable and actionable at scale, and who is able to productively partner with multiple stakeholders at multiple levels throughout the organization.</p><p><strong>When: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p> <strong>Discover your role:</strong></p><ul><li>Define and drive the holistic data strategy for modelling and managing connected scientific data in the data lake, ensuring data flowing in from transactional lab informatics systems is harmonized, contextualized, and connected.</li><li>Partner with data engineering to define and shape the ingestion, transformation, and integration pipelines (ETL/ELT) that move data from transactional lab informatics systems into the data lake and turn it into connected, production-grade data products.</li><li>Own the product vision, roadmap, and backlog for scientific data products, prioritizing based on scientific value, downstream demand, and organizational impact.</li><li>Design and govern data models that capture the relationships across scientific entities (e.g., compounds, biologics, samples, assays, experiments, results, instruments, and study metadata) so that data is connected rather than isolated.</li><li>Translate the needs of scientific, Digital & Technology, and analytics stakeholders into clear data product requirements, acceptance criteria, and delivery plans, and drive outcomes that are aligned with all stakeholders, as well as with the corporate Digital and Transformation strategy.</li><li>Partner with Digital & Technology teams that consume connected data products from the data lake for analysis and reporting, ensuring data products meet their integration, quality, and access requirements.</li><li>Partner with data scientists seeking connected scientific datasets, ensuring datasets are analytics-ready, well-documented, and fit for modelling and AI/ML use cases.</li><li>Establish and uphold data quality, governance, lineage, metadata, and FAIR (Findable, Accessible, Interoperable, Reusable) principles across scientific data products.</li><li>Conceive, elicit, and champion the use of AI-driven approaches for searching and discovering structured scientific data, improving how users find and connect relevant datasets.</li><li>Act as the primary point of contact and advocate for scientific data products, gathering feedback and continuously improving usability, coverage, and value.</li></ul><p><strong>This role requires:</strong> </p><ul><li>BS/BA degree and/or MS degree in a related field required.</li><li>10+ years of progressive experience managing scientific laboratory data, ideally within the biopharmaceutical or life sciences industry.</li><li>Strong scientific background (e.g., chemistry, biology, molecular biology, biochemistry, immunology, pharmacology, or a related discipline), with the ability to understand the meaning and context of the data being modelled.</li><li>Hands-on experience with data modelling and an understanding of how to connect data across multiple source systems.</li><li>Ability to drive diverse stakeholders to alignment on desired outcomes, and to influence others at multiple levels without direct authority.</li><li>Working knowledge of data engineering concepts — data pipelines, ETL/ELT, and data transformation — sufficient to define requirements for and collaborate effectively with data engineers.</li><li>Strong SQL skills, plus proficiency in a primary Databricks language (e.g., SQL, Python/PySpark).</li><li>Familiarity with transactional lab informatics systems such as ELN, LIMS, and instrument or analytical data platforms.</li><li>Product ownership or product management experience, including roadmap definition, backlog prioritization, and stakeholder management.</li><li>Strong communication skills and the ability to bridge scientific, technical, and analytics audiences.</li><li>Advanced degree in a biology discipline required; PhD in molecular biology, biochemistry, genetics, or immunology preferred.</li></ul><p><strong>Strongly Desired</strong></p><ul><li>Hands-on experience with Databricks (or a comparable lakehouse platform) for managing and delivering data products.</li><li>Experience leveraging AI to search, discover, and interrogate structured data.</li><li>Experience with knowledge graphs, ontologies, controlled vocabularies, or semantic data models for connecting scientific entities.</li><li>Understanding of data lake / lakehouse architectures and modern data engineering practices.</li><li>Experience working with data scientists and analytics teams to deliver analytics-ready datasets.</li></ul><p><strong>Nice to Have</strong></p><ul><li>Familiarity with data governance frameworks and FAIR data principles in regulated and unregulated environments.</li><li>Experience with metadata management, data cataloging, and data lineage tooling.</li><li>Experience with AI/ML workflows and the data requirements that support them.</li><li>Awareness of regulatory and compliance considerations relevant to pharmaceutical R&D data.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Portfolio Management]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49940]]></requisitionid>
    <referencenumber><![CDATA[R49940]]></referencenumber>
    <apijobid><![CDATA[r49940]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49940/senior-manager-portfolio-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Senior Manager, Portfolio Management is responsible for executing key portfolio management processes and supporting the execution of portfolio planning and review activities across Global Research and Development. This role serves as a strategic partner to the Director of Portfolio Management, translating complex portfolio information into actionable insights, facilitating cross-functional alignment, and driving the execution of portfolio operating processes that support informed decision-making.</p><p>The successful candidate will independently lead assigned portfolio management workstreams, develop executive and c-suite ready analyses and high-quality communications, and partner with stakeholders across Clinical Development, Corporate Strategy, Finance, Operations, and other functions to improve portfolio visibility, planning, and execution. Portfolio review frameworks, planning activities, portfolio reporting, prioritization discussions, and portfolio operating processes are recurring responsibilities within the team's work.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li></ul><br><h3>Discover your role:</h3><h3><strong>Portfolio Reviews & Planning Execution</strong></h3><ul><li>Accountable for the planning and execution of assigned portfolio reviews and portfolio planning activities, including timelines, deliverables, stakeholder engagement, content integration, and meeting readiness.</li><li>Lead cross-functional preparation efforts to ensure portfolio discussions are supported by accurate, timely, and decision-relevant information.</li><li>Partner with stakeholders across the enterprise including Clinical Development Units, Development Program Management, Resource Management, Corporate Strategy, Finance, and several other functions to consolidate portfolio inputs, develop insights and ensure alignment on key messages and discussion topics.</li><li>Support the Director of Portfolio Management in enterprise-level portfolio reviews and other strategic portfolio initiatives.</li></ul><h3><strong>Portfolio Assessment & Decision Support</strong></h3><ul><li>Develop portfolio analyses that identify execution risks, portfolio constraints, milestone impacts, prioritization challenges, and opportunities requiring management attention.</li><li>Assess portfolio trends and emerging issues to support discussions regarding resource allocation, portfolio trade-offs, and execution planning.</li><li>Develop clear recommendations, high-quality discussion materials, and accurate supporting analyses for leadership review.</li><li>Support the Director of Portfolio Management in evaluating broader portfolio scenarios, prioritization discussions, and portfolio optimization opportunities.</li></ul><h3><strong>Portfolio Operating Processes</strong></h3><ul><li>Accountable for the delivery of assigned portfolio management processes and ensure consistent execution, defined deliverables, and ongoing process improvement.</li><li>Establish and maintain standardized templates, workflows, and operating procedures that improve efficiency, transparency, and consistency across portfolio activities.</li><li>Monitor process performance and recommend enhancements to improve the quality and effectiveness of portfolio management activities.</li><li>Support the Director of Portfolio Management in evolving portfolio management capabilities and operating models.</li></ul><h3><strong>Executive Communications & Portfolio Reporting</strong></h3><ul><li>Develop insightful, clear and compelling executive and c-suite presentations, portfolio summaries, briefing materials, and leadership communications that synthesize portfolio information into concise and actionable insights.</li><li>Accountable for recurring portfolio reporting activities, including status updates, portfolio summaries, milestone tracking, and leadership communications.</li><li>Track and communicate key portfolio developments, risks, actions, and outcomes arising from portfolio review discussions and planning activities.</li></ul><h3><strong>Cross-Functional Portfolio Partnership</strong></h3><ul><li>Serve as the primary portfolio management partner for assigned therapeutic areas, functions, portfolio segments, or review processes.</li><li>Support cross-functional working sessions to align stakeholders on portfolio assumptions, risks, dependencies, and recommendations.</li><li>Build productive relationships across stakeholder groups and facilitate resolution of issues affecting portfolio planning and execution.</li><li>Support the Director of Portfolio Management in engaging senior leaders and preparing for portfolio-related discussions and decision forums.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Minimum Master's degree in a scientific, business, or related field.</li><li>8+ years of experience in portfolio/program management, strategy consulting, business operations, strategic planning, pharmaceutical development, or related functions.</li><li>Demonstrated experience leading cross-functional initiatives.</li><li>Strong analytical, problem-solving, and critical-thinking skills.</li><li>Demonstrated ability to navigate ambiguity, manage multiple priorities, and bring structure, clarity, and momentum to complex, highly matrixed environments.</li></ul><h3><strong>Preferred</strong></h3><ul><li>Experience supporting pharmaceutical R&D or development portfolios.</li><li>Experience developing well-crafted executive-level presentations communications.</li><li>Familiarity with portfolio planning, prioritization, resource management, and portfolio review processes.</li><li>Experience working with senior leadership teams and enterprise-level initiatives.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Specialist, On the floor (Overnights)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49582]]></requisitionid>
    <referencenumber><![CDATA[R49582]]></referencenumber>
    <apijobid><![CDATA[r49582]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49582/quality-assurance-specialist-on-the-floor-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support QA initiatives for a broad range of topics relative to the start-up and operations of a drug product facility. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work model, available shifts:</p><ul><li><p>3rd shift, Friday-Tuesday, 10pm-8:30am</p></li><li><p>3rd shift, Monday-Friday, 10pm-8:30am</p></li></ul></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Work on and potentially lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team</p></li><li><p>Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures</p></li><li><p>Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.</p></li><li><p>Maintain project timelines to support the evolving business</p></li><li><p>Perform on-the-floor quality review of documents, such as: equipment logs, training records, testing results, batch records and supporting documents</p></li><li><p>Review and approval of documents (electronic and paper-based)</p></li><li><p>Provide mentorship during on-the-floor manufacturing</p></li><li><p>Support audits, inspections and investigations</p></li><li><p>Perform quarantine, segregation of material and line clearances</p></li><li><p>Contribute to the continuous improvement initiatives</p></li><li><p>Adjust schedule based on facility start up, filling, and manufacturing needs</p></li><li><p>Collaborate with cross-functional internal teams</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Requires B.S in life sciences or related field; may substitute proven experience for education requirement</p><ul><li><p>Assoc QA Specialist : 2+ years of experience</p></li><li><p>QA Specialist : 4 + years of experience</p></li></ul></li></ul><p>Level will be determined based on experience</p><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family Care Benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 10:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Facilities Maintenance Scheduler & Planner]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47525]]></requisitionid>
    <referencenumber><![CDATA[R47525]]></referencenumber>
    <apijobid><![CDATA[r47525]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47525/senior-facilities-maintenance-scheduler-planner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an experienced Maintenance Planner & Scheduler to join our Facilities Operations and Engineering team, supporting our multi-building research campus in an on-site work model. In this role, you will prioritize, coordinate, and optimize preventive, predictive, and corrective maintenance for MEP, HVAC, refrigeration, and other critical facility systems, safeguarding asset reliability and minimizing operational disruptions, while collaborating with technicians, engineers, contractors, and materials management teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model: On-site</li></ul><br><h3>Discover your role:</h3><ul><li>Review new service requests and convert them into detailed CMMS work orders with clear scope, labor hours, and safety requirements</li><li>Develop and publish weekly/daily schedules that align with technician availability and research-critical maintenance windows</li><li>Craft or update standardized job plans, task lists, and PM templates to ensure consistent execution across all buildings</li><li>Coordinate materials, spare parts, and contractor services to ensure everything is staged before work begins</li><li>Supervise work order progress, adjust schedules for emergent priorities, and close out completed jobs with accurate documentation</li><li>Communicate status, constraints, and upcoming activities to Facilities Operations, Engineering, and lab stakeholders</li></ul><h3>This role requires:</h3><ul><li>Associate Degree in Electrical, HVAC, or Mechanical Engineering (10+ years of relevant experience accepted in lieu of degree)</li><li>5+ years of maintenance planning, industrial maintenance, or utilities operations experience</li><li>Strong grasp of HVAC, refrigeration, boiler, chilled-water, and electrical distribution systems</li><li>Proven expertise with commercial/industrial MEP systems and CMMS software (TRIRIGA, Maximo, SAP PM) in addition to Microsoft Office tools</li><li>Balancing multiple priorities in regulated or mission-critical environments</li><li>Clear communication, anticipating issues, and keeping projects on track with minimal direction</li><li>Collaborating with technicians, engineers, and vendors to solve maintenance challenges</li><li>Organizing complex information into clear, actionable plans</li><li>CMRP or equivalent planning/scheduling certification preferred</li><li>Valid New York State driver's license</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Instrumentation & Controls Engineer]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49591]]></requisitionid>
    <referencenumber><![CDATA[R49591]]></referencenumber>
    <apijobid><![CDATA[r49591]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49591/senior-instrumentation-controls-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior Instrumentation & Controls (I&C) Engineer </strong>to join our <strong>Site Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Acting as the primary I&C representative within multidisciplinary project teams for projects from concept development through design, construction, commissioning, qualification and handover</li><li>Coordinating with Process, Mechanical, Electrical, Maintenance, Operations and Quality groups</li><li>Providing technical leadership for instrumentation and control systems across manufacturing, utility and facility infrastructure projects</li><li>Supporting troubleshooting and root cause investigations associated with instrumentation and control system performance issues</li><li>Specifying and evaluating field instrumentation including pressure, temperature, flow, level, load cells, pH, conductivity, TOC, UV and analytical instrumentation</li><li>Leading design reviews and approving instrumentation philosophies, P&IDs, instrument indexes, I/O lists, control narratives, loop drawings and vendor packages</li><li>Participating in HAZOPs, risk assessments, constructability reviews and design verification activities</li><li>Reviewing and approving instrumentation wiring diagrams, panel designs and control architecture</li><li>Establishing, maintaining and continuously improving site instrumentation and controls engineering standards and specifications</li><li>Providing technical direction to engineering consultants, system integrators and construction contractors</li><li>Leading technical assessments for equipment obsolescence, instrument upgrades and functional equivalency evaluations</li><li>Supporting FAT, SAT, commissioning, qualification and startup activities for new systems and modifications</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have excellent technical and analytical skills</li><li>Problem-solving and continuous improvement skills</li><li>You possess strong communication and collaboration skills</li><li>You are adaptable and can work in a fast-paced, regulated environment</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Bachelor’s degree in Instrumentation Engineering, Electrical Engineering, Automation Engineering or related discipline.</li><li>Minimum 8 years of engineering experience with increasing responsibility in instrumentation, controls and automation systems.</li><li>Demonstrated experience leading I&C engineering activities for projects within pharmaceutical, biotechnology or other highly regulated industries.</li><li>Strong knowledge of process instrumentation, industrial control systems and GMP regulated manufacturing environments.</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Assoc QC Micro Analyst]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45671]]></requisitionid>
    <referencenumber><![CDATA[R45671]]></referencenumber>
    <apijobid><![CDATA[r45671]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45671/temp-assoc-qc-micro-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking an Associate QC Micro Analyst to join our Quality Control Microbiology team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Shift Requirements: Shift pattern may be required based on business needs</p></li><li><p>Location: Raheen, Limerick, Ireland</p></li><li><p>This is a 12-month contract position</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Perform microbiological testing and environmental monitoring activities to support product quality and patient safety</p></li><li><p>Review laboratory data, support investigations, and maintain compliance with quality and regulatory standards</p></li><li><p>Collaborate with cross-functional teams to support manufacturing operations and continuous improvement initiatives</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Thrive in laboratory, manufacturing, and cleanroom environments</p></li><li><p>Demonstrate strong attention to detail and a commitment to quality</p></li><li><p>Work effectively both independently and within cross-functional teams</p></li><li><p>Maintain accuracy and compliance while managing competing priorities</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Requires BS/BA in Life Sciences or related field or equivalent combination of education and experience</p></li><li><p>For Associate QC Micro Analyst: 0-2 years of relevant experience</p></li><li><p>For QC Micro Analyst: 2+ years of relevant experience, preferably in the pharmaceutical or biotechnology industry</p></li></ul><p>Thrive today. Grow tomorrow.</p><p>#LI-Onsite #REGNIRLQC</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 08:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist – CRISPR Screening, target identification]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50092]]></requisitionid>
    <referencenumber><![CDATA[R50092]]></referencenumber>
    <apijobid><![CDATA[r50092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50092/scientist-crispr-screening-target-identification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Scientist to join our Oncology & Immuno-Oncology group, supporting the identification and validation of novel tumor drug targets using in vitro and in vivo approaches. In this role, you will design and execute cell-based and animal studies that directly inform target discovery and validation, while collaborating closely with your supervisor and cross-functional peers to move promising science forward.<br><br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.<br><br><strong>When & where:</strong><br><br>* Location: Tarrytown, NY<br>* Work model/flexibility: Onsite<br><br><strong>Discover your role:</strong><br><br>* Perform in vitro cell culture and molecular biology experiments to support target discovery<br>* Conduct in vivo tumor studies in mice, including injections, and blood and tissue collection<br>* Analyze and document data with rigor, then communicate findings clearly to your supervisor and peers<br>* Compile and organize results into polished, presentation-ready formats<br>* Maintain precise, well-organized lab notebooks<br>* Keep the lab running smoothly through daily maintenance tasks, such as ordering reagents and supplies<br>* Thrive in a fast-paced, team-driven environment where priorities can shift day to day<br>* Bring curiosity and initiative to learning new techniques and expanding your skill set<br><br><strong>This role requires:</strong><br><br>* BS or MS with at least 3 years of relevant work experience<br>* Experience with mouse tumor models, including subcutaneous implantation, drug dosing, tumor measurement, and tumor harvest<br>* Experience with large-scale mammalian cell culture<br>* Experience with basic molecular biology and biochemistry techniques (e.g., cell/tissue lysate preparation for DNA/RNA/protein analysis, western blots, transfection, PCR, and cloning)<br>* Strong organizational and communication skills, with the ability to work well in a team<br>* Preferred: experience designing FACS panels and performing multi-color FACS analysis<br>* Preferred: experience with CRISPR screening.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager - Finance]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47683]]></requisitionid>
    <referencenumber><![CDATA[R47683]]></referencenumber>
    <apijobid><![CDATA[r47683]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47683/associate-manager-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Associate Manager Finance – International Financial Planning to join our Finance team, supporting our international finance operations. In this role, you will support financial analysis, forecasting, budgeting, and legal entity financial planning activities while collaborating with Finance colleagues, Country Finance Directors, Accounting, Tax, Treasury, country leadership, and other CFO functions. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Prepare and maintain legal entity Actuals, budget, and forecast profit and loss statements by product for markets outside the United States.</p></li><li><p>Conduct Actuals versus Forecast analysis and support critical business decisions through regular and ad hoc financial analysis.</p></li><li><p>Partner with Country Finance Directors, country leadership, and Finance colleagues to support financial planning and analysis processes across international legal entities.</p></li><li><p>Review Actuals data, advise on appropriate coding, and coordinate corrections with Accounting to support accurate financial reporting and analysis.</p></li><li><p>Prepare quarterly legal entity review decks, maintain international office dashboards and trackers, and support external audits with financial analysis and data.</p></li><li><p>Develop cash flow forecasts with Treasury, support tax-related analyses with Tax, and manage accruals, prepayments, and budget/forecast system data loads.</p></li><li><p>Support facilities-related financial activities, including cost tracking, vendor onboarding, purchase requisitions and purchase orders, and landlord payment accounting.</p></li><li><p>You approach complex challenges proactively, remain effective in ambiguity, and consider issues from multiple perspectives.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Relevant undergraduate degree and professional finance qualification such as ACA, CMA, ACCA, CIMA, CPA, or equivalent.</p></li><li><p>Minimum 5 years of progressive finance-related experience, including at least 2 years of post-qualification experience where applicable.</p></li><li><p>Experience in financial planning and analysis, budgeting, forecasting, profit and loss management, and variance analysis.</p></li><li><p>Ability to prepare and maintain legal entity financial reporting, dashboards, trackers, review materials, and management analysis.</p></li><li><p>Experience supporting accruals, prepayments, cash flow forecasting, headcount tracking, and financial data management.</p></li><li><p>Experience working with budget and forecast systems, financial coding reviews, and financial reporting accuracy processes.</p></li><li><p>Ability to support external audits and provide financial analysis for taxation-related processes, special projects, and ad hoc business requests.</p></li><li><p>Knowledge of facilities-related financial administration, including cost tracking, vendor onboarding, purchase requisitions, purchase orders, and rent-related accounting support.</p></li><li><p>Commitment to ensuring full compliance with Regeneron standard operating procedures and policies.</p></li><li><p>Fluent English communication skills; additional languages spoken in India are advantageous.</p></li><li><p>Ability to deal with ambiguity, demonstrate persistence and proactivity, and assess issues from different perspectives.</p></li><li><p>Experience in the biotechnology, pharmaceutical, or Shared Service Centre environment is a plus.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, CMC Regulatory Affairs]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50070]]></requisitionid>
    <referencenumber><![CDATA[R50070]]></referencenumber>
    <apijobid><![CDATA[r50070]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50070/associate-manager-cmc-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, CMC Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan organization in a hybrid work mode. In this role, you will support regulatory CMC strategy and submissions across therapeutic areas while collaborating with Global Regulatory CMC, CMC Regulatory Science, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Working model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Support planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplement submissions.</li><li>Prepare Japanese application forms and regulatory dossiers for high-quality submissions.</li><li>Support regulatory decision-making with cross-functional teams based on local requirements.</li><li>Act as a local liaison with PMDA for CMC submissions and information requests.</li><li>Assess CMC change controls against regulatory filings to maintain compliance.</li><li>Review manufacturing processes and specifications for investigational product release requests.</li><li>Monitor project timelines to support on-time regulatory submissions.</li><li>You thrive in a collaborative environment and communicate effectively across global teams.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in a scientific discipline; Master's degree preferred.</li><li>Strong biopharmaceutical and regulatory Chemistry, Manufacturing and Controls (CMC) background.</li><li>10+ years of regulatory CMC experience, including health authority interactions, major submissions, and approvals in Japan.</li><li>Experience supporting CTN, J-NDA, eCTD submissions, PCA, MCN, and PMDA responses.</li><li>Knowledge of Japanese regulatory requirements, guidance documents, and regulatory resources.</li><li>Experience participating in agency meetings and supporting regulatory communications.</li><li>Ability to obtain and maintain Foreign Manufacturing Accreditation or Foreign Manufacture Registration.</li><li>High fluency in Japanese and English.</li><li>Ability to interpret regulations, communicate effectively, and contribute strategically.</li><li>Strong work ethic with the ability to collaborate across teams and apply lessons learned.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 21 Aug 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Submission Project Management]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44752]]></requisitionid>
    <referencenumber><![CDATA[R44752]]></referencenumber>
    <apijobid><![CDATA[r44752]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44752/manager-regulatory-submission-project-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager Regulatory Submission Project Management Japan to join our Regulatory Operations team, supporting our Japan regulatory business area in a hybrid work model. In this role, you will drive timely, compliant regulatory submissions while collaborating with Regulatory Publishing, vendors, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><p><strong>Discover your role:</strong></p><p>• Ensure consistency and standardization across regulatory submissions.<br>• Support PMDA consultations, Clinical Trial Notifications, PCAs, MCNs, and NDAs.<br>• Track submission deliverables in Veeva Vault RIM through submission objects and metadata.<br>• Manage submission readiness with Regulatory Publishing and external vendors.<br>• Support eCTD preparation within defined business timelines.<br>• Review submission content plans for compliance with health authority and ICH guidelines.<br>• Guide teams on document uploads and submission-related issue resolution.<br>• You thrive in a fast-paced environment with changing priorities.</p><p><strong>This role requires:</strong></p><p>• Bachelor’s degree or equivalent experience.<br>• 6+ years of pharmaceutical industry or related experience.<br>• Fluency in Japanese and proficiency in English.<br>• Strong knowledge of PMDA, MHLW, ICH, and applicable regulatory requirements.<br>• Experience with submission processes and systems, including Veeva Vault RIM and docuBridge.<br>• Strong eCTD knowledge and experience.<br>• Experience with Microsoft Office applications and Adobe Acrobat.<br>• Ability to manage firm deadlines and adapt quickly to changing priorities.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50178]]></requisitionid>
    <referencenumber><![CDATA[R50178]]></referencenumber>
    <apijobid><![CDATA[r50178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50178/senior-manager-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Global Procurement International Markets UK France to join our Global Procurement team, supporting our international markets organization in a hybrid work model. In this role, you will drive indirect and commercial procurement activities across the UK and France while collaborating with country stakeholders, international market leads, and global category teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Uxbridge, United Kingdom</p><p>Work model: Hybrid</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead procurement activities across the UK and France markets.</p></li><li><p>Implement global category strategies within local markets.</p></li><li><p>Provide country input to strengthen global category strategies.</p></li><li><p>Execute sourcing, negotiation, contracting, and supplier management activities.</p></li><li><p>Partner with stakeholders on budgets, spend planning, and future business needs.</p></li><li><p>Review local contracts and analyze spend trends and patterns.</p></li><li><p>Drive procurement process consistency and best practices across international markets.</p></li><li><p>You build strong relationships and influence stakeholders to deliver results.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Experience in Indirect Procurement and/or Commercial Procurement.</p></li><li><p>Bachelor’s degree in a relevant field and progressive procurement experience.</p></li><li><p>Experience in procurement within the pharmaceutical or biopharmaceutical industry preferred.</p></li><li><p>Experience leading or supporting global category teams, suppliers, and procurement processes.</p></li><li><p>Expertise in sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Knowledge of local market requirements and supply markets.</p></li><li><p>Experience using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Ability to deliver cost savings, cash flow improvements, and category value.</p></li><li><p>Strong data analysis and data-driven decision-making skills.</p></li><li><p>Experience coaching procurement professionals and leading teams preferred.</p></li><li><p>Working knowledge of sourcing, contracting, ERP, and eRFx systems, including Oracle, Zycus, GEP, Ariba, or similar tools.</p></li><li><p>Proficiency with Word, Excel, and PowerPoint.</p></li><li><p>Strong stakeholder management skills and ability to operate effectively in ambiguous environments.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - South West England]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45109]]></requisitionid>
    <referencenumber><![CDATA[R45109]]></referencenumber>
    <apijobid><![CDATA[r45109]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45109/sales-specialist-south-west-england/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Sales Specialists at Regeneron are at the forefront of engaging key professionals and customers. We are looking for someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. We are driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p>This role is focused on the maintenance and growth of key accounts within the South West England territory.</p><p><strong>As a Sales Specialist, a typical day may include the following:</strong></p><ul><li>Developing, implementing and supervising territory account plans based on market insights. Ensure continuous and timely updates to the plan in response to changing market dynamics.</li><li>Outstanding account management and operational excellence applying key data sources to strategically develop a territory account plan. And to supervise and progress activity and sales metrics.</li><li>Working closely with alliance partners to develop innovative solutions whilst adhering to SOP’s, regulatory, legal compliance guidelines and ABPI Code</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Ability to work across multiple indications in a specialist therapeutic area.</li><li>Leading with the Science and put the patient front and centre of all we do. Ensure patient access through partnering with key customer stakeholders</li></ul><h3>This role may be for you if:</h3><ul><li>You are confident in demonstrating strong and consistent sales performance that goes above and beyond related to product goals</li><li>Innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>Have a competitive spirit and harness your “grit” to power your approach to sales, collaborating effectively with internal and external partners</li><li>Share a passion for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>Are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree and, at least, 5 years' pharmaceutical sales experience. Previous respiratory or specialist medicine experience desired but not essential. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Product Management - Delivery & Operations Product Lead - Medical Affairs Domain]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47701]]></requisitionid>
    <referencenumber><![CDATA[R47701]]></referencenumber>
    <apijobid><![CDATA[r47701]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47701/senior-manager-product-management-delivery-operations-product-lead-medical-affairs-domain/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Global Development IT (GDIT) is seeking an experienced and motivated Senior Manager with deep technical and functional expertise in Veeva CRM, Veeva Medical Vault, Medical Affairs systems and AI. This role is responsible for end-to-end implementation, support and continuous improvement of technology products and data within the Medical Affairs domain. This role will also work closely with their business counterparts, Business Process Owners, Subject Matter Experts, Training, Process and Procedures and Corporate Enterprise IT. </p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead detailed business and technical requirements' analysis for Veeva Medical CRM, Veeva Medical Vault and Medical Affairs systems, translating Medical processes into scalable, complaint system designs.</p></li><li><p>Configure and optimize Veeva CRM components, including but not limited to: Medical Inquiry, Call Reporting, Key Medical Insights, Events, Approved email, Consent Management, Page layout, Profiles, Permission sets and Sharing Rule.</p></li><li><p>Design and configure Veeva Vault Medical Vault objects, relationships, lifecycles, workflows, user roles, document types, and metadata to support scientific content management and medical review processes.</p></li><li><p>Define and support AI-driven Medical Affairs workflows including automated medical inquiry categorization, sentiment and topic analysis of MSL interactions, and proactive identification of emerging medical insights.</p></li><li><p>Collaborate with Global Development and IT team members to extract insights from CRM and other data sources using AI and digital tools.</p></li><li><p>Define and maintain Veeva data models and data quality standards to enable AI/ML readiness, ensuring alignment across CRM and Vault platforms, including reference data, picklists, field dependencies, and master data governance.</p></li><li><p>Partner with integration teams to design and validate integrations using Veeva APIs, Vault APIs, middleware platforms, and standard connectors with systems such as MDM, ERP, data lakes, and analytics tools.</p></li><li><p>Collaborate with global stakeholders in Medical Affairs, GDIT functions, Corporate IT and other relevant functions to support multi-country deployments, localization, and regulatory requirements across FDA, EMA, and other regional compliance frameworks.</p></li></ul><p><strong> This Job might Be for you if you have:</strong></p><ul><li><p>Knowledge of Medical Affairs business processes, systems and key trends in the Industry.</p></li><li><p>Experience on Jira, Agile product management, backlog management, Scrum and Kanban boards.</p></li><li><p>Technical Experience and ability to Partner with data science and integration teams to build, validate, and operationalize AI solutions using APIs, middleware, and AI/ML platforms (e.g., NLP, large language models, predictive analytics).</p></li><li><p>Proven track record of managing competing priorities across a multitude of stakeholders, and to lead teams to deliver value-oriented, prioritized solutions. </p></li><li><p>Excellent interpersonal skills, and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience </p></li><li><p>Experience managing technology capability identification, selection, implementation, and operations </p></li><li><p>Excellent problem-solving skills to address day-to-day challenges associated with business solutions </p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>A BS/BA Degree with 8+ years of relevant experience, or a MS Degree with 6+ years relevant experience</p></li></ul><ul><li><p>Experience partnering with technology teams and driving value in the Medical Affairs space with specific technologies like Veeva Medical CRM, Veeva Medical Vault, Salesforce</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - JACKSON, MS]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48056]]></requisitionid>
    <referencenumber><![CDATA[R48056]]></referencenumber>
    <apijobid><![CDATA[r48056]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48056/medical-account-specialist-ii-neurology-jackson-ms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Jackson]]></city>
    <state><![CDATA[Mississippi]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Jackson (Metro), MS</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - HOUSTON (NORTH), TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48060]]></requisitionid>
    <referencenumber><![CDATA[R48060]]></referencenumber>
    <apijobid><![CDATA[r48060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48060/medical-account-specialist-ii-neurology-houston-north-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Houston North (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - AUSTIN, TX]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48062]]></requisitionid>
    <referencenumber><![CDATA[R48062]]></referencenumber>
    <apijobid><![CDATA[r48062]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48062/medical-account-specialist-ii-neurology-austin-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Austin]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Austin (Metro), TX</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div></div><div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - CHICAGO North IL]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48050]]></requisitionid>
    <referencenumber><![CDATA[R48050]]></referencenumber>
    <apijobid><![CDATA[r48050]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48050/medical-account-specialist-ii-neurology-chicago-north-il/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Chicago North (Metro), Illinois </p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY -LOS ANGELES, CA]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48079]]></requisitionid>
    <referencenumber><![CDATA[R48079]]></referencenumber>
    <apijobid><![CDATA[r48079]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48079/medical-account-specialist-ii-neurology-los-angeles-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Los Angeles (Metro), CA</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48464]]></requisitionid>
    <referencenumber><![CDATA[R48464]]></referencenumber>
    <apijobid><![CDATA[r48464]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48464/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Uxbridge, UK</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Advocacy]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48324]]></requisitionid>
    <referencenumber><![CDATA[R48324]]></referencenumber>
    <apijobid><![CDATA[r48324]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48324/associate-director-global-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[[Unknown]]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Global Patient Advocacy, Hematology-Oncology to cover International and US markets. In this role, you will lead the development and execution of patient advocacy strategies, building meaningful relationships with advocacy groups and professional societies to support patient needs and business objectives, while collaborating with cross-functional leaders (Medical Affairs, Market Access, Marketing, and Policy teams). This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><p>UK, Germany, Italy or Spain (Hybrid model)</p><p>Travel: 40%+</p><h3>Discover your role:</h3><ul><li><p>Lead advocacy and engagement strategy for Hematology-Oncology in Europe</p></li><li><p>Partner with senior cross-functional leaders to build advocacy strategies</p></li><li><p>Build and manage relationships with patient advocacy groups and professional societies</p></li><li><p>Oversee patient engagement initiatives, meetings, and communications</p></li><li><p>Develop frameworks to embed the patient perspective across organizational processes</p></li><li><p>Track and report outcomes of advocacy initiatives to senior leadership</p></li><li><p>You foster collaboration and consensus among diverse stakeholders</p></li><li><p>You drive a patient-centric culture and influence strategic decisions</p></li></ul><h3>This role requires:</h3><ul><li><p>Undergraduate degree required</p></li><li><p>10+ years of industry or relevant professional experience</p></li><li><p>5+ years of patient advocacy, stakeholder engagement, and issues management</p></li><li><p>European, international, or global advocacy experience and understanding of relevant regulations (e.g., EMA, HTA)</p></li><li><p>Proven leadership in developing and executing advocacy strategies</p></li><li><p>Country-level advocacy work experience preferred</p></li><li><p>Multilingual capabilities strongly preferred</p></li></ul><div><div><div></div></div></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - MANHATTAN, NY]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48010]]></requisitionid>
    <referencenumber><![CDATA[R48010]]></referencenumber>
    <apijobid><![CDATA[r48010]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48010/medical-account-specialist-ii-neurology-manhattan-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Manhattan]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance.</p><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Manhattan (NY Metro), NY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals</li><li>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade</li><li>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team.</li><li>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations)</li><li>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives.</li><li>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products</li><li>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share</li><li>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts.</li><li>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus</li><li>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred.</li><li>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Results oriented with a proven track record of success with product launches</li><li>Strong account management experience with analytical, problem-solving and planning skills</li><li>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks</li><li>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace</li></ul><p><strong>Salary range (annually) </strong><br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Canada]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46239]]></requisitionid>
    <referencenumber><![CDATA[R46239]]></referencenumber>
    <apijobid><![CDATA[r46239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46239/associate-director-finance-administration-canada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are hiring an Associate Director, Finance & Administration to partner closely with country leadership and commercial teams, supporting high‑impact business decisions through financial insight, forecasting, and analysis. This role sits at the centre of the country organisation, working across Finance, Accounting, Tax, Treasury, and global CFO functions to shape commercial performance, governance, and long‑term planning.</p><p>If you enjoy combining critical thinking with hands‑on delivery—and value visible ownership at country level—this is a role where your expertise will genuinely influence outcomes.</p><h3>What You’ll Be Doing:</h3><ul><li><p>Partnering with country leadership on budgeting, forecasting, and financial planning</p></li><li><p>Preparing and presenting forecasts, including actuals versus forecast analysis</p></li><li><p>Managing resource planning, including FTE utilisation across cost centres</p></li><li><p>Supporting commercial teams with P&L ownership and profitability insights</p></li><li><p>Translating epidemiology and commercial data into financial forecasts</p></li><li><p>Coordinating with Accounting on revenue accuracy, accruals, and reporting</p></li><li><p>Acting as a local finance liaison across Tax, Treasury, and CFO functions</p></li><li><p>Ensuring compliance with internal policies and external regulations</p></li></ul><h3>This Role May Be For You If:</h3><ul><li><p>You enjoy working closely with senior collaborators to support sound decisions</p></li><li><p>You like roles that balance strategic perspective with practical execution</p></li><li><p>You are comfortable partnering across commercial, medical, and G&A teams</p></li><li><p>You value clear country ownership and accountability</p></li><li><p>You enjoy collaborating with global and local finance colleagues</p></li><li><p>You are motivated by improving processes and strengthening governance</p></li></ul><h3>To Be Considered:</h3><p>You will have a relevant undergraduate degree, along with a postgraduate qualification (such as an MBA) and/or a recognised professional finance qualification. You will bring at least five years of post‑qualification finance experience, primarily within the biotech or pharmaceutical industry, including experience supporting commercial P&Ls. Fluency in English and the local country language is required. International experience and additional language skills are an advantage.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director–Data Lake Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47775]]></requisitionid>
    <referencenumber><![CDATA[R47775]]></referencenumber>
    <apijobid><![CDATA[r47775]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47775/associate-director-data-lake-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>About Regeneron</strong> </p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p><div><p>As an Associate Director, Data Lake Operations, you will lead the design, implementation, and management of clinical data lake solutions supporting global clinical trial and healthcare research initiatives. You will ensure efficient data ingestion, integration, and governance while enabling advanced analytics, regulatory compliance, and informed decision-making.</p><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Defining and executing the strategy and roadmap for the Clinical Data Lake aligned with business and regulatory objectives</p></li><li><p>Leading the design, development, and implementation of scalable data lake architectures across clinical data ecosystems</p></li><li><p>Building and managing data pipelines integrating diverse sources (EDC systems, lab data, biomarker data, EHR, and other healthcare datasets)</p></li><li><p>Ensuring data security, privacy, and compliance with regulatory standards such as GDPR, HIPAA, FDA, and ICH-GCP</p></li><li><p>Establishing standardized clinical data models aligned with CDISC standards (SDTM, ADaM) to enable analytics and reporting</p></li><li><p>Driving data quality, transformation, validation, and lineage tracking to ensure integrity and traceability of clinical data</p></li><li><p>Collaborating with IT, data teams, and global stakeholders to align data infrastructure with business objectives</p></li><li><p>Leading matrixed teams across data engineering, ingestion, standardization, and visualization functions</p></li><li><p>Driving innovation through adoption of new technologies and data capabilities to enhance clinical insights and decision-making</p></li></ul><h3><strong>This job may be for you if you have:</strong></h3><ul><li><p>Strong expertise in data lake architecture, data engineering, and clinical data ecosystems</p></li><li><p>Deep understanding of clinical trial processes, CDISC standards (SDTM, ADaM), and regulatory requirements</p></li><li><p>Experience working with big data platforms such as AWS, Spark, or Google Cloud</p></li><li><p>Strong proficiency in database technologies (SQL, NoSQL) and ETL tools</p></li><li><p>Proven ability to lead cross-functional teams and manage complex stakeholder environments</p></li><li><p>Strong strategic thinking, problem-solving, and communication skills</p></li><li><p>Experience integrating data from multiple sources and building scalable data solutions</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>Bachelor’s or Master’s degree in Computer Science, Data Science, Bioinformatics, or a related field</p></li><li><p>10+ years of experience in data management, data engineering, or clinical operations</p></li><li><p>At least 5+ years of leadership experience managing teams or large-scale data initiatives</p></li><li><p>Proven experience working on large-scale data lake implementations in healthcare or clinical research domains</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director - Hematology (Mid Atlantic)]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48919]]></requisitionid>
    <referencenumber><![CDATA[R48919]]></referencenumber>
    <apijobid><![CDATA[r48919]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48919/regional-director-hematology-mid-atlantic/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong>The Regional Director (RD), Hematology will report to the National Business Director, Hematology and be responsible for hiring, leading, developing and retaining the Hematology Medical Specialist team in the Great Plains region to support our Multiple Myeloma Bispecific Antibody.</p><p>The RD is responsible for ensuring strong and consistent sales performance that meet or exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Hematology market. The RD will work closely with their cross functional partners to ensure full cooperation and transparency within the region. The RD will work closely with Training and Development to ensure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field Role</p></li><li><p><strong>Location: </strong><strong>Mid Atlantic Region- SC, NC, VA, WV, MD, DE, NJ, Eastern PA</strong></p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Build and develop a high integrity, high quality sales team and provide overall leadership to the team.</p></li><li><p>Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p></li><li><p>Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p></li><li><p>Ensure each employee is trained on, and effectively implements, customer education.</p></li><li><p>Communicate most current knowledge of the industry and competitor products to regional teams.</p></li><li><p>Ensure participation in industry related trade shows, meetings, conferences, etc.</p></li><li><p>Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p></li><li><p>Allocate and manage the region's budget and utilization of promotional resources.</p></li><li><p>Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p></li><li><p>Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Oncology, preferably Hematology.</p></li><li><p>Experience in Biologics and buy and bill products or strong relevant experience in the Oncology field required. Experience in hematology oncology a strong plus.</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p></li><li><p>Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p></li><li><p>Strong ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel extensively with local and regional influence.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Marketing - Oncology]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49102]]></requisitionid>
    <referencenumber><![CDATA[R49102]]></referencenumber>
    <apijobid><![CDATA[r49102]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49102/manager-marketing-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Country Marketing, Oncology to join our Commercial Oncology team, supporting our Japan business in a hybrid work mode. In this role, you will lead local oncology brand marketing strategy and execution across commercialised indications and future launches, while collaborating with cross-functional and cross-regional collaborators including Medical Affairs and the Sales Team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Japan. Hybrid work model. Travel required 30–40%, including some weekends for conferences and meetings.</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead local oncology brand strategy and provide input to global brand plans.</li><li>Drive the brand planning process, analysing competition and identifying promotional opportunities.</li><li>Partner with Medical Affairs to create and agree an aligned brand strategy.</li><li>Deliver external collaborator engagement plans, including national congresses and HCP meetings.</li><li>Manage the local promotional budget and spend against approved limits.</li><li>You develop customer-focused, differentiated messages for key target audiences.</li><li>You collaborate with the Sales Team on Field Plans of Action and communications.</li><li>You uphold the highest ethical and compliance standards in every action.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree, with preference for a science background.</li><li>5+ years of biotech or pharmaceutical brand marketing experience.</li><li>Working knowledge of local healthcare compliance codes and promotional regulations.</li><li>Expertise managing advertising agencies and suppliers, and developing annual budgets.</li><li>Excellent planning, prioritization, communication and presentation skills.</li><li>Written and spoken English language skills.</li><li>Oncology marketing experience preferred; product launch experience a plus.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Market Access]]></title>
    <date><![CDATA[Sun, 12 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48268]]></requisitionid>
    <referencenumber><![CDATA[R48268]]></referencenumber>
    <apijobid><![CDATA[r48268]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48268/associate-manager-market-access/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Market Access Associate Manager, Rare Disease Portfolio, Japan, to join our Market Access team, supporting our Japan affiliate in a hybrid work model. In this role, you will drive launch, pricing, and reimbursement strategies for the rare disease portfolio while collaborating with commercial, marketing, HEOR (health economics and outcomes research), medical affairs, clinical, and global market access strategy teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Tokyo, Japan</li><li>Hybrid working model</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Drive pricing and reimbursement submissions to the National Health Insurance (NHI) price listing.</li><li>Prepare reimbursement dossiers and execute price negotiations aligned with product strategy.</li><li>Monitor reimbursement and policy shifts, pricing, and HTA (health technology assessment) rule changes.</li><li>Provide Japan-specific insights to shape value and evidence strategies.</li><li>Develop and maintain reimbursement tracking tools and annual tactical plans.</li><li>Build and maintain external relationships with key stakeholders, including MHLW (Ministry of Health, Labour and Welfare), HTA bodies, and key opinion leaders (KOLs).</li><li>You collaborate effectively across teams to ensure alignment with Japan-specific priorities.</li><li>You adapt to evolving challenges and provide strategic insights to inform decisions.</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree required.</li><li>Native-level Japanese language proficiency.</li><li>Strong verbal and written communication skills.</li><li>In-country market access experience, including knowledge of Japan’s reimbursement environment, payer systems, and cost comparator pricing methodology.</li><li>Project and process management skills with the ability to prioritize tasks effectively.</li><li>Preferred: Experience in rare diseases, cell or gene therapy launches, and HTA negotiation in Japan.</li><li>NHI price negotiation experience with authorities in Japan.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Commercial Operations (f/m/d)]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45302]]></requisitionid>
    <referencenumber><![CDATA[R45302]]></referencenumber>
    <apijobid><![CDATA[r45302]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45302/director-commercial-operations-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We’re looking for a Director Commercial Operations to join our team in Munich, supporting our commercial business across Germany<strong>.</strong> This is an impactful role focused on translating strategic commercial plans into flawless local execution. You’ll partner closely with sales, marketing, and training teams to drive operational perfection, while helping ensure alignment with regulatory standards and evolving business priorities.You'll be joining a dynamic global team, with the opportunity to craft how we deliver commercial support to field-based teams in a fast-paced and highly collaborative environment.</p><p><strong>Where:</strong></p><p>Munich, Germany</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Providing strategic and operational leadership to Commercial Operations teams.</p></li><li><p>Translating global commercial strategies into locally relevant, tactical plans.</p></li><li><p>Supervising performance analytics and reporting to advise business decisions.</p></li><li><p>Handling key Sales Operations activities such as field sizing, onboarding, communications, and incentive tracking.</p></li><li><p>Partnering with Commercial Training to coordinate development for field-based staff.</p></li><li><p>Supporting the localization of promotional materials with Marketing and IT.</p></li><li><p>Collaborating with Compliance and Internal Audit teams to maintain adherence to internal policies and external regulations.</p></li><li><p>Building strong relationships with field managers to proactively identify and resolve operational issues.</p></li><li><p>Coordinating contracts and logistics for Speaker Programs and Advisory Boards.</p></li><li><p>Ensuring oncology meetings, sponsorships, and events align with business needs.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>You enjoy redefining big-picture strategy into practical local execution.</p></li><li><p>You’re comfortable collaborating across departments and geographies.</p></li><li><p>You bring structure and accountability to multi-stakeholder projects.</p></li><li><p>You thrive in complex environments where priorities shift and evolve.</p></li><li><p>You’ll need to bring significant leadership experience in Commercial Operations within the German (bio-)pharmaceutical industry.</p></li><li><p>A strong grasp of market dynamics, local laws, and reporting requirements is important.</p></li><li><p>Confidence navigating analytics, experience with tools like PowerPoint, Excel, Veeva, and Word</p></li><li><p>Fluency in German and English</p></li><li><p>Prior experience supporting field sales in a pharma setting is desirable</p></li><li><p>A Bachelor’s degree and at least 10 years of industry experience, including 5 years in global commercial operations.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>125.250,00 € - 208.750,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - NEUROLOGY - ATLANTA South, GA]]></title>
    <date><![CDATA[Wed, 22 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48027]]></requisitionid>
    <referencenumber><![CDATA[R48027]]></referencenumber>
    <apijobid><![CDATA[r48027]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48027/medical-account-specialist-ii-neurology-atlanta-south-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Atlanta]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong> </p></div><div><p>The Rare Neurology Medical Account Specialist (MS) engages Neurology specialists and key stakeholders across diverse care settings (e.g., academic centers, large group practices, IDNs, and community accounts) within an assigned geography. The MS delivers clinically focused messaging to drive revenue and achieve product goals, demonstrating strong ownership, initiative, and compliant, integrity-driven performance. </p></div><div></div><div><p>This role involves developing and executing account strategies to grow market share, building relationships with clinicians, nurses, and patient advocacy groups, and collaborating with cross-functional partners (e.g., Reimbursement and Access, Regional Science Managers) to address customer needs and market dynamics. The MS also supports sales success through participation in congresses, regional meetings, and other industry events. </p></div><div></div><div><p><strong>When & where: </strong> </p></div><div><ul><li><p>Field Based </p></li></ul></div><div><ul><li><p>Location: Atlanta South (Metro), GA</p></li></ul></div><div></div><div><p><strong>Discover your role: </strong> </p></div><div><ul><li><p>Engage Rare Neurology Experts and other key Rare Neurology customers within an assigned geography and deliver clinically focused selling messages to launch product and grow brand share and revenue and to consistently deliver product goals </p></li></ul></div><div><ul><li><p>Partner with multiple collaboration stakeholders; Reimbursement and Access Specialists and other stakeholders to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives in assigned territory </p></li></ul></div><div><ul><li><p>Develops strong working relationships with customers, collaboration colleagues and Internal contacts - Clinics, physicians, nurses, additional important health care providers, key patient advocacy support groups, collaboration teammates, Reimbursement and Access Specialist team, Clinical Nurse Educators, Marketing, National Accounts, Training and Trade </p></li></ul></div><div><ul><li><p>Conducts rare neurology-specific market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems by the rare neurology account team. </p></li></ul></div><div><ul><li><p>Deep knowledge of applicable customers and markets (prescribers/HCPs/institutions/ organizations) </p></li></ul></div><div><ul><li><p>Strategic account selling and management skills. Develop comprehensive territory/account/customer plans to drive achievement of desired objectives. </p></li></ul></div><div><ul><li><p>Consistently demonstrates emphasis on the “total account call” insuring that all personnel in the account are educated on commercially available Regeneron products </p></li></ul></div></div><div><div><ul><li><p>Develop strategy and execute tactics within key accounts in the Rare Neurology therapeutic area to establish, generate and expand market share </p></li></ul></div><div><ul><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Rare Neurology account team, e.g. supports contracting pull-through with accounts. </p></li></ul></div><div><ul><li><p>Gains deep knowledge of each assigned account through internal research and proactive gathering and integration of information from various stakeholders within the account, e.g. business model, relevant business metrics, unique challenges, and strategic goals. </p></li></ul></div><div></div><div><p><strong>This role requires: </strong> </p></div><div><ul><li><p>Bachelor’s degree mandatory, Master’s degree or additional advanced education/certifications a plus </p></li></ul></div><div><ul><li><p>Minimum 5 years successful experience in Neurology sales and specialty/biologic/REMS products strongly preferred. Launch experience, preferred. </p></li></ul></div><div><ul><li><p>Minimum of (2) years of experience working with key thought leaders or high influence customers in large group practices, academic hospitals, or managed care organizations with a concentration in Neurology </p></li></ul></div><div><ul><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines </p></li></ul></div><div><ul><li><p>Results oriented with a proven track record of success with product launches </p></li></ul></div><div><ul><li><p>Strong account management experience with analytical, problem-solving and planning skills </p></li></ul></div><div><ul><li><p>Current account management experience in calling on large Neurology group practices and/or integrated delivery networks </p></li></ul></div><div><ul><li><p>Strong understanding of the Neurology therapeutic area and the current Neurology marketplace </p></li></ul></div><div></div><div><p><strong>Salary range (annually) </strong> <br>$158,950 - $220,000 (Please note: this is the accurate range for this position; other ranges shown may reflect system defaults.) </p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$0.00 - $0.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Heidelberg - Mainz - Trier - Saarbrücken]]></title>
    <date><![CDATA[Sun, 26 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48524]]></requisitionid>
    <referencenumber><![CDATA[R48524]]></referencenumber>
    <apijobid><![CDATA[r48524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48524/sales-specialist-immunology-fmd-heidelberg-mainz-trier-saarbruecken/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Respiratory division at key meetings. You will identify the key people in Pneumology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><p><strong>Where:</strong></p><p>Field based in the territory: <strong>Heidelberg - Mainz - Trier - Saarbrücken</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</p></li><li><p>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</p></li><li><p>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</p></li><li><p>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</p></li><li><p>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</p></li><li><p>Regular reporting to the sales management</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Deep understanding of the local healthcare economy, with the ability to identify key players in Pneumology</p></li><li><p>“Patient first” value system</p></li><li><p>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</p></li><li><p>5+ years of sales experience within the biotech/pharmaceutical sector</p></li><li><p>Respiratory experience is preferred</p></li><li><p>Proficiency in German as well as conversational English</p></li><li><p>Readiness for very frequent travel and a driver's license cl. 3/B.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist, Product Biochemistry]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49521]]></requisitionid>
    <referencenumber><![CDATA[R49521]]></referencenumber>
    <apijobid><![CDATA[r49521]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49521/scientist-product-biochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Scientist</strong> to join our Product Biochemistry team, on-site in Tarrytown, NY. In this role, you will support late-stage development (Phase II through commercialization) of biologics, developing and deploying analytical methods and purification strategies, enriching and characterizing product variants, and helping onboard new technologies that deepen product understanding and improve processes across the pipeline.</p><p>This position offers the opportunity to bring scientific creativity, efficiency, and flexibility to a fast-paced, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site in Tarrytown, NY</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support laboratory operations</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Develop analytical methods and purification protocols to support extended characterization of therapeutic proteins and gene therapy vectors</li><li>Conduct biochemical/biophysical characterization to support development, regulatory submissions, and commercialization</li><li>Apply DOE, advanced statistics, and risk assessments to evaluate and optimize methods and processes</li><li>Design and execute experiments to enrich, purify, and characterize size/charge variants, complexes, and high-concentration formulations</li><li>Independently operate U/HPLCs and AKTA FPLCs, and perform capillary-based electrophoresis</li><li>Integrate learnings from internal data and external literature to make science-based study design recommendations</li><li>Author high-quality technical documents (protocols, reports, memos), contribute to regulatory sections and publications, and ensure timely documentation of experiments in accordance with established SOPs and guidelines</li><li>Document experiments, results, and findings in the electronic laboratory notebook, and present work at group and department meetings</li><li>Maintain instruments, troubleshoot instrumental/experimental problems, order/maintain supplies, and improve lab/data workflows within your area of expertise</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>This is a hands-on, on-site laboratory role requiring independent operation of specialized analytical instrumentation and the ability to manage multiple priorities in a fast-moving R&D environment.</li><li>Flexibility to thrive in a fast-paced, team environment while also working independently across multiple projects, and to mentor others while contributing to a safe, efficient, and inclusive lab environment, is required.</li></ul><h3><strong>Let's find out if we're a fit:</strong></h3><h3>Must-haves:</h3><ul><li>BS/MS in Biochemistry, Biophysics, Engineering, or a related field, with 8-10+ years of relevant industry experience</li><li>Strong lab skills in protein separation, purification, and tangential flow filtration (TFF), and skills in protein/product identification using mass spectrometry</li><li>Excellent oral and written communication skills and evidence of teamwork</li><li>Strong initiative to complete tasks, learn new technologies, and demonstrate a commitment to continuous learning</li><li>Ability to communicate clearly, transparently, and in a timely manner with key stakeholders</li></ul><h3>Preferred / nice-to-haves:</h3><ul><li>Technical proficiency in automated FPLC and/or HPLC (SEC, IEX, affinity), electrophoresis (capillary or microchip, SDS-PAGE, western blots), spectroscopy, and light scattering</li><li>Fundamental understanding of protein structure/function, mass spectrometry, and immunology/immunogenicity</li><li>Experience working in the biopharmaceutical industry</li></ul><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Statistical Genetics - Regeneron Genetics Center]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48469]]></requisitionid>
    <referencenumber><![CDATA[R48469]]></referencenumber>
    <apijobid><![CDATA[r48469]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48469/associate-manager-statistical-genetics-regeneron-genetics-center/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Regeneron Genetics Center uses genetics and health data on millions of people to advance our understanding of human disease and guide Regeneron’s therapeutic programs. We are looking for a Statistical Geneticist to build tools, workflows, and applications to analyze and interpret the genetics of nearly 3 million individuals linked with rich phenotype data from around the world. You will build and maintain a suite of tools to manage, execute, and assess genome-wide analyses leading to new discoveries and insights into disease mechanisms. Within the broad domain of cardiovascular, metabolic, and skeletal diseases, you will work collaboratively with other specialists in genomic data analysis, translational genetics, functional biology, and medicine, to enable Regeneron to create better medicines for patients in need. </p><p><strong> </strong></p><div><p><strong>When & where: </strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><ul><li><p>Perform genome-scale analyses with genotype, imputed, and sequence data from millions of individuals across hundreds of relevant phenotypes and biomarkers. </p></li><li><p>Work across teams to build, maintain, and improve analytical workflows that implement analytical best practices.</p></li><li><p>Build and manage systems to execute genomic analysis on a large scale and at high throughput. This including tools for analysis tracking and post-analysis quality control.</p></li><li><p>Employ your expertise in genetic analysis to identify and troubleshoot analyses at scale.</p></li><li><p>Test and integrate computational tools for deployment across our collection of diverse quantitative, health outcomes, and molecular data types.</p></li><li><p>Critically review and provide input on analysis plans, results, and summaries to ensure accuracy and reliability. Identify problems and propose solutions or analytical refinements.</p></li><li><p>Have experience in the analysis of large genetic association studies and meta-analysis, including through the analysis of UK Biobank or other biobank-scale data.</p></li><li><p>Have experience in the management of genetic and phenotype data in human genetic studies, including familiarity manipulating sequence data (e.g., VCF files), strategies for genotype imputation, and for quality control of genetic association inputs and outputs.</p></li></ul><p><strong> </strong></p><p>This role requires: </p><ul><li><p>PhD in Human Genetics, Biostatistics, or a related field</p></li><li><p>0-2 years of experience, postdoctoral training or relevant industry experience is preferred</p></li><li><p>Experience and competence with approaches currently employed in the group, including genome- and exome-wide association analysis, rare variant analysis, Mendelian randomization, LD Score regression, polygenic risk score modelling, meta-analysis, and the use of functional data to prioritize variants and genes of interest. </p></li><li><p>Expertise with cloud computing environments, advanced tools for genomic analyses (PLINK, REGENIE, etc.)</p></li><li><p>Statistical analysis and computation (R, Python, C/C++) are necessary</p></li><li><p>Experience working in cardiovascular, metabolic, and/or musculoskeletal diseases is preferred. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Statistical Programming]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46205]]></requisitionid>
    <referencenumber><![CDATA[R46205]]></referencenumber>
    <apijobid><![CDATA[r46205]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46205/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager, Statistical Programming</strong> to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In this role, you will drive high-quality programming deliverables from single studies through regulatory approval, product launch, and beyond, while collaborating with partnering functions, external service providers, and study teams. This position offers the opportunity to shape department strategy and mentor talent within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><strong>Location:</strong> Warren, NJ or Cambridge, MA</li><li><strong>Work model/flexibility:</strong> hybrid-onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead programming support across multiple studies, ensuring timely, high-quality deliverables</li><li>Coordinate programming documentation and specifications, following established standards</li><li>Champion company values through excellence, collaboration, and accountability</li><li>Communicate proactively with study and project teams to clarify requirements and guide programmers</li><li>Lead submission-ready programming deliverables for global regulatory authority filings</li><li>Drive department goals and serve as a subject matter expert on key topics</li><li>Guide the development of direct reports through goal-setting, coaching, and mentoring</li><li>Contribute to hiring by screening and interviewing programming candidates</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You bring advanced SAS skills honed in a clinical data environment, ideally across multiple therapeutic areas</li><li>You understand pharmaceutical clinical development, statistical concepts, and regulatory submission requirements</li><li>You collaborate naturally across global, interdisciplinary teams</li><li>You juggle multiple projects and priorities without losing sight of quality</li><li>You solve problems with initiative, creativity, and a self-starter mindset</li><li>You enjoy influencing, mentoring, and coaching others toward strong results</li><li>You lead with accountability and hold yourself to a high bar</li><li>You're energized by both hands-on programming work and people leadership</li></ul><p><strong>This role requires:</strong></p><ul><li>Advanced SAS programming expertise in a clinical data environment</li><li>Strong understanding of clinical trial principles and regulatory submission requirements</li><li>Proven ability to lead global, cross-functional teams</li><li>Experience managing multiple concurrent projects and priorities</li><li>Demonstrated mentoring or coaching experience with junior programmers</li><li><strong>Education & experience:</strong> MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline, with 10+ years (12+ for BS) of programming experience — preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including some project and people management experience</li><li><strong>Preferred/nice to haves:</strong> Knowledge of additional programming languages such as R or Python</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Statistical Programming]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49715]]></requisitionid>
    <referencenumber><![CDATA[R49715]]></referencenumber>
    <apijobid><![CDATA[r49715]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49715/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming, Central Services to join our Statistical Programming team, supporting our Central Services function in a hybrid work model. In this role, you will lead statistical programming activities across integrated data and reporting, regulatory submissions, exploratory analyses, and clinical trial disclosure while collaborating with Statistical Programming, Biostatistics, Clinical Transparency and Trial Disclosure, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Location: Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead programming support for integrated datasets, pooled analyses, and reporting deliverables across assigned projects.</p></li><li><p>Create and maintain programming documentation, including integrated dataset specifications such as pooled ADaM datasets, following established standards and processes.</p></li><li><p>Support the creation and review of electronic data packages for regulatory submissions to ensure compliance with regulatory, industry, and internal standards.</p></li><li><p>Coordinate with Clinical Transparency and Trial Disclosure, Biostatistics, Statistical Programming, and cross-functional teams to deliver disclosure-ready datasets and outputs.</p></li><li><p>Provide technical expertise in developing tools, standard processes, and programming solutions that improve efficiency and compliance.</p></li><li><p>Troubleshoot and resolve complex programming and submission-related issues while supporting inspection readiness activities and regulatory inquiries.</p></li><li><p>Collaborate effectively across teams to achieve submission and reporting objectives in a highly regulated environment.</p></li><li><p>Guide and support team members in developing their technical skills and knowledge of submission programming.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related field.</p></li><li><p>7+ years of programming experience, preferably processing clinical trial data within the biotechnology, pharmaceutical, or health-related industry.</p></li><li><p>Proven experience in regulatory submissions and compliance with global standards, including FDA, European Medicines Agency (EMA), Pharmaceuticals and Medical Devices Agency (PMDA), and Clinical Data Interchange Standards Consortium (CDISC) requirements.</p></li><li><p>Proficient SAS programming skills in a clinical data environment with expertise in at least one, preferably multiple, therapeutic areas.</p></li><li><p>Strong understanding of CDISC standards, including Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM), and Define-XML.</p></li><li><p>Proficiency with Pinnacle 21 (P21), including experience reviewing and troubleshooting P21 reports and issues.</p></li><li><p>Good knowledge of electronic Common Technical Document (eCTD) regulatory submission formats.</p></li><li><p>Experience with project and people management, including leading teams and managing deliverables.</p></li><li><p>Strong problem-solving skills with the ability to handle complex technical and programming challenges.</p></li><li><p>Proficiency with SAS Base, Stat, Macro, and Graph.</p></li><li><p>Excellent communication and interpersonal skills, with the ability to collaborate across functional areas.</p></li><li><p>Strong attention to detail and the ability to manage multiple priorities in a fast-paced environment.</p></li><li><p>SAS certification is a plus.</p></li><li><p>Knowledge of open-source programming languages such as R and/or Python is a plus.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Auditory Disorders]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49650]]></requisitionid>
    <referencenumber><![CDATA[R49650]]></referencenumber>
    <apijobid><![CDATA[r49650]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49650/senior-scientist-auditory-disorders/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Scientist to lead the Physiology function within our Auditory research team. In this role, you will lead the design and execution of experiments to interrogate mechanisms of pathology, identify novel therapeutic targets, and contribute to therapeutic design, validation, and pre-clinical testing, while collaborating with a cross-functional team to develop new medicines for hearing loss and vestibular disorders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and characterize novel animal models to understand mechanisms of hearing loss and vestibular dysfunction and test novel therapeutics</li><li>Design and perform in vivo functional assays (e.g., ABR, DPOAE, VsEPs, noise exposure experiments) and other novel technologies to study hearing loss mechanisms</li><li>Conduct histological analyses of the inner ear to examine cell morphology and subcellular protein localization</li><li>Design rigorous experiments to address core scientific questions and carefully analyze and evaluate data</li><li>Present data internally and externally, contributing to discussions in a collaborative, cross-functional team environment</li><li>Contribute to writing protocols, reports, and articles for publication</li><li>Manage several concurrent studies with strong attention to detail and organization</li><li>Motivate and develop research associates and other trainees while exploring uncharted scientific territory</li></ul><p><strong>This role requires:</strong></p><ul><li>Ph.D. in a relevant field or Au.D.</li><li>Strong background in electrophysiology and ear biology</li><li>Experience with functional measures of ear physiology in mice and/or other animal models</li><li>Strong communication and presentation skills, with the ability to work well independently and in a team</li><li>Preferred: familiarity with stereotaxic delivery to the inner ear</li><li>Preferred: experience with primary culture of auditory, vestibular, or neural cells</li><li>Preferred: excellent publication record and managerial experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Obesity, Muscle & Metabolism]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47888]]></requisitionid>
    <referencenumber><![CDATA[R47888]]></referencenumber>
    <apijobid><![CDATA[r47888]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47888/senior-scientist-obesity-muscle-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Scientist to join our Obesity, Metabolism and Muscle Diseases Group, supporting the identification and validation of novel drug targets for metabolic disorders. In this role, you will design and conduct in vitro and in vivo studies to advance target validation and mechanistic understanding, while collaborating and communicating efficiently across the Obesity, Metabolism and Muscle Diseases Group and other teams and functions.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Identify and implement novel areas, technologies, and approaches for validating targets and target modalities in metabolic disease drug discovery</p></li><li><p>Design and conduct in vitro assays to support target validation</p></li><li><p>Design and perform in vivo studies in animal models to support target validation and mechanistic understanding</p></li><li><p>Analyze data and draw scientifically sound conclusions</p></li><li><p>Provide timely updates on scientific progress, communicating efficiently across teams and functions</p></li><li><p>Thrive in a fast-paced, multi-project environment, staying detail-oriented and well-organized</p></li><li><p>Work well both independently and as part of a team</p></li><li><p>Bring curiosity and a desire to expand your areas of expertise as new questions arise</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D. with a minimum of 3 years of post-doctoral research experience</p></li><li><p>Broad expertise in biochemistry, molecular biology, in vitro assay development, and in vivo techniques</p></li><li><p>Ability to independently design and perform complex in vivo studies, interpret data, and summarize results</p></li><li><p>Expertise in at least one metabolism research area (e.g., diabetes, endocrinology, obesity, lipid and energy metabolism)</p></li><li><p>Excellent communication and presentation skills, with a documented strong scientific record</p></li><li><p>Preferred: strong understanding of human and mouse genetics</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49456]]></requisitionid>
    <referencenumber><![CDATA[R49456]]></referencenumber>
    <apijobid><![CDATA[r49456]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49456/executive-medical-director-clinical-program-lead-immunology-rheumatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Medical Director to join our Hematology team, providing overall clinical scientific leadership for our non I/O BCMA program. You'll be responsible for our clinical development strategy and execution of clinical trials in this area, partnering closely with the Global Program Head to design the optimal development strategy for this portfolio. You'll serve as a clinical role model for the team, bringing outstanding clinical scientific knowledge to hematology clinical research and leading a team of MDs and clinical scientists. You'll report directly to the VP, Therapeutic Area Lead, Hematology.</p><p>This position offers the opportunity to provide clinical scientific leadership on a fast-growing, science-driven cell therapy program making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Travel: 10% to relevant conferences/congresses</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards</p></li><li><p>Uses excellent scientific standing among peers and the ability to address issues with scientific rigor and creative solutions; uses that creativity and knowledge to build and defend data-driven plans and decisions, both with internal scientific management and the Company's partners/collaborators</p></li><li><p>Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape; designs and develops smaller, yet robust and innovative FIH as well as Phase 2/3 programs</p></li><li><p>Drives strong consensus-building skills and the ability to lead multi-disciplinary teams towards sound decision-making; leads dynamic and matrixed clinical teams in a fast-paced and hands-on environment</p></li><li><p>Leads and develops a team of MDs and clinical scientists to meet business needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An advanced degree in medicine (MD or equivalent) required; Specialized fellowship training in Immunology or Rheumatology preferred.</p></li><li><p>A minimum of 6-8 years of industry experience in related therapeutic area clinical development is preferred</p></li><li><p>Demonstrated consistent track record in a range of leadership roles, including working with senior clinical development staff and establishing credibility with external collaborators such as opinion leaders and regulators</p></li><li><p>Substantial experience in drug development, including experience with both IND and BLA/NDA submission</p></li><li><p>Experience leading study start-up, directing and guiding study team execution, data cleaning, medical review, database locks, and handling health authority responses</p></li><li><p>A strong commitment to impacting patients through drug development and the ability to work well within a team setting</p></li><li><p>People management experience is a plus</p></li></ul><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - LAS VEGAS, NV]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48931]]></requisitionid>
    <referencenumber><![CDATA[R48931]]></referencenumber>
    <apijobid><![CDATA[r48931]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48931/medical-account-specialist-ii-hematology-las-vegas-nv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Nevada]]></city>
    <state><![CDATA[Nevada]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Las Vegas/Flagstaff</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - KENTUCKY]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48945]]></requisitionid>
    <referencenumber><![CDATA[R48945]]></referencenumber>
    <apijobid><![CDATA[r48945]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48945/medical-account-specialist-ii-hematology-kentucky/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Louisville-Jefferson County5]]></city>
    <state><![CDATA[Kentucky]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: Louisville or Lexington, KY</li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Cloud Development Security and Operations Engineer]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47382]]></requisitionid>
    <referencenumber><![CDATA[R47382]]></referencenumber>
    <apijobid><![CDATA[r47382]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47382/principal-cloud-development-security-and-operations-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>The Regeneron Genetics Center Information Technology team is looking for a passionate Principal Cloud Development, Security, and Operations Engineer with strong technical ability, communication, and collaboration skills. You will be responsible for the design and implementation of cloud infrastructure, automation, security controls, and compliance processes on Amazon Web Services, supporting data, High-Performance Computing, Artificial Intelligence, and microservice platforms used by research scientists and bioinformaticians. You will work hands-on to build and implement cloud Development, Security, and Operations solutions, embed security into system design, and provide technical support and guidance to end users and internal teams. You will also provide technical mentorship for Lead and Senior Development, Security, and Operations engineers and coordinate with Information Security, Privacy, and internal Information Technology teams to ensure security, scalability, and reliability of the Regeneron Genetics Center cloud platform.</p><p><strong>When & where:</strong></p><p><strong>Location:</strong> Tarrytown, NY</p><p><strong>Work model/flexibility:</strong> 4 days onsite</p><p><strong>Discover your role:</strong></p><ul><li><p>Design and implement infrastructure-as-code, automation scripts, and Continuous Integration/Continuous Delivery pipelines supporting data, High-Performance Computing, Artificial Intelligence, and microservice platforms on Amazon Web Services.</p></li><li><p>Embed security controls into system design and implementation, including Identity and Access Management policies, network segmentation, secrets management, and compliance validation pipelines.</p></li><li><p>Design and implement tools to automate operational processes across Regeneron Genetics Center's cloud and systems engineering platforms.</p></li><li><p>Support all audit-related activities, including providing evidence and remediation of findings for the Regeneron Genetics Center cloud platform.</p></li><li><p>Develop and implement continuous delivery systems and Continuous Integration/Continuous Delivery methodologies for Regeneron Genetics Center's systems engineering platforms using both Amazon Web Services services and GitHub Actions, Actions Runner Controller self-hosted runners on Elastic Kubernetes Service, and Static Application Security Testing/Dynamic Application Security Testing integration.</p></li><li><p>Recommend and deploy monitoring, metrics, and logging systems on Regeneron Genetics Center cloud engineering platforms.</p></li><li><p>Identify and implement opportunities to build systems that are highly available, scalable, and self-healing.</p></li><li><p>Develop Standard Operating Procedures and configure cloud services to support compliance validation.</p></li><li><p>Provide technical support, training, and documentation to end users and research teams using Regeneron Genetics Center's data, High-Performance Computing, Artificial Intelligence, and microservice platforms.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's Degree in Computer Science or a related field.</p></li><li><p>8+ years of in-depth Amazon Web Services experience and relevant security certifications.</p></li><li><p>Hands-on experience designing and implementing cloud infrastructure automation, Continuous Integration/Continuous Delivery pipelines, infrastructure-as-code, and security controls.</p></li><li><p>Solid understanding of cloud security posture, including Identity and Access Management, network segmentation, secrets management, compliance validation, and security-by-design principles.</p></li><li><p>Experience supporting data, High-Performance Computing, Artificial Intelligence, or microservice platforms in a technical or user-facing capacity.</p></li><li><p>Knowledge of core Amazon Web Services including Elastic Compute Cloud, Elastic Block Store, Simple Storage Service, Elastic Load Balancing, Relational Database Service, Elastic Kubernetes Service, and Identity and Access Management.</p></li><li><p>Tangible experience with Linux administration and automation of security controls and compliance validation.</p></li><li><p>Experience with monitoring tools such as Splunk, Grafana, and Prometheus.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Real-World Data and Analytics (HEOR)]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49657]]></requisitionid>
    <referencenumber><![CDATA[R49657]]></referencenumber>
    <apijobid><![CDATA[r49657]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49657/senior-manager-real-world-data-and-analytics-heor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Real-World Data and Analytics (RWDnA) will support the generation of real-world evidence (RWE) in oncology by delivering data-driven insights through the analysis of real-world data (RWD). The individual will contribute to query/protocol/statistical analysis (SAP) development and execute analyses of RWD to support the generation of RWE to address research questions. The successful candidate will conduct hands-on programming on internal RWD assets, support publication activities, and participate in vendor management.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Sleepy Hollow, NY</p><p><strong>Discover your role:</strong><br>• Contribute to the development of RWE queries, protocols, and statistical analysis plans (SAPs) within oncology<br>• Translate analytic findings into clear insights and communicate them directly to project teams<br>• Support end-to-end RWE query and study delivery, including hands-on programming and quality control of analytic code<br>• Evaluate and identify appropriate real-world data sources to address specific research questions<br>• Contribute to scientific communications, including abstracts, posters, manuscripts, and internal presentations<br>• Support senior team members in coordinating activities with external analytics vendors and research partners</p><p><strong>This role requires:</strong><br>• Doctoral degree in a quantitative field focused on the application of data science to healthcare data with 2+ years of hands-on programming experience; or a Master's degree in a related field with 4+ years of hands-on programming experience<br>• Hands-on experience with real-world data sources such as large-scale administrative claims data (e.g., Optum, Medicare, Komodo claims) and electronic health records (EHRs)<br>• Experience in oncology research and with oncology-specific real-world data (e.g., Flatiron, ConcertAI)<br>• Advanced programming capabilities using SAS and R<br>• Proficiency in statistical methodologies including survival analysis, propensity score methods, and generalized linear models.<br>• Experience with machine learning approaches applied to real-world data<br>• Excellent written and verbal communication skills<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Automation]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47040]]></requisitionid>
    <referencenumber><![CDATA[R47040]]></referencenumber>
    <apijobid><![CDATA[r47040]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47040/manager-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are looking for a Manager Automation to supervise a team responsible for cGMP automation quality systems, software change control, and automation related corrective actions. The Manager Automation develops procedures and methods for executing automation projects and support activities, while coaching and developing Automation professionals. This group ensures manufacturing systems are operating as expected and provides time-sensitive fixes to keep manufacturing running. This is a dynamic role that focuses on providing impeccable customer service, while developing direct reports to ensure their continued success and growth. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Troy, NY</li><li>Work model: Monday-Friday 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Manage the performance, training, development, and results of the team</li><li>Provide technical and automation support to manufacturing</li><li>Oversee activities related to the configuration and support of manufacturing process equipment and the maintenance of cGMP software administration program</li><li>Manage periodic evaluation reports for automated systems used in commercial manufacturing</li><li>Oversee the investigation of manufacturing deviations and anomalies related to automation and software</li><li>Manage projects related to corrective action or equipment performance improvement.</li><li>Implement modification/change control procedures and protocols.</li><li>Support Validation with initial design review, software testing and protocol review</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA in Engineering, software programming, or a related field, along with 6+ years of experience with automated equipment in the pharmaceutical or biopharmaceutical industry for Associate Manager, 7+ years for Manager, and 8+ years for Senior Manager.</li><li>1 to 3+ years of supervisory experience required, depending on level (Associate Manager, Manager, or Senior Manager).</li><li>1+ year of direct experience in the design, installation, maintenance, or troubleshooting of automated control systems.</li><li>Understanding of bioprocessing and testing software, cGMP software quality principles, and data integrity regulations.</li><li>Demonstrated ability to mentor and empower a team of automation professionals under demanding timelines.</li><li>Ability to organize and present technical overviews to engineering staff, multi-functional departments, and management.</li><li>Strong communication skills across all levels and a blend of business and technical savvy.</li><li>Commitment to compliance with regulatory, corporate, and site-specific policies and procedures.</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$103,300.00 - $231,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45330]]></requisitionid>
    <referencenumber><![CDATA[R45330]]></referencenumber>
    <apijobid><![CDATA[r45330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45330/senior-manager-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Pharmacovigilance Safety Operations Japan to join our Global Patient Safety team, supporting our Japan business in a hybrid work mode. In this role, you will oversee Japan pharmacovigilance reporting and compliance activities while collaborating with cross-functional teams, external partners, and service providers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Japan</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Serve as the primary contact for Japan ICSR, research report, and FSMT activities.</li><li>Review vendor-prepared safety evaluations and PMDA submissions for accuracy.</li><li>Oversee pharmacovigilance service providers and monitor contract compliance.</li><li>Drive process improvements that strengthen quality and compliance.</li><li>Author and update working instructions and deliver related training.</li><li>Contribute to J-RMP development and execution activities.</li><li>Partner with external departments and license partners on safety deliverables.</li><li>You build collaborative relationships to support effective safety outcomes.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>More than 7 years of pharmacovigilance and post-marketing surveillance operations experience.</li><li>Strong knowledge of PMDA, MHLW, and International Council for Harmonisation guidelines and regulations.</li><li>Experience supporting Japan aggregate reporting and local pharmacovigilance activities.</li><li>Experience managing external service providers and vendor relationships.</li><li>Experience supporting J-NDA safety content and responding to PMDA inquiries.</li><li>Experience with regulatory inspections, including PMDA re-examination, MAH license renewal, or GCP reliability inspection.</li><li>Experience leading complex projects, including team improvement, safety database implementation, or safety data migration initiatives.</li><li>Experience collaborating with Medical Affairs, Regulatory Affairs, Sales and Marketing, and Clinical Development teams.</li><li>Prior global pharmacovigilance experience.</li><li>Strong project management and cross-functional collaboration skills.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Director, Hematology, Japan]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49676]]></requisitionid>
    <referencenumber><![CDATA[R49676]]></referencenumber>
    <apijobid><![CDATA[r49676]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49676/sales-director-hematology-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sales Director, Hematology Japan</strong> to join our <strong>Commercial Oncology team</strong>, leading our <strong>Japan Hematology business</strong>. In this role, you will <strong>lead the hematology field sales organization, drive commercial execution, and deliver strong sales performance aligned with company goals</strong> while collaborating with <strong>cross-functional stakeholders, commercial operations, and marketing teams</strong>. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead and develop a high-performing hematology sales team.</li><li>Drive sales performance that meets or exceeds brand objectives.</li><li>Coach, develop, and retain talent through feedback and development planning.</li><li>Create national, regional, and local account plans with measurable tactics.</li><li>Oversee CRM use, sales analytics, and business key performance indicators.</li><li>Build relationships with key healthcare professionals across oncology.</li><li>Partner with cross-functional teams to address market trends and opportunities.</li><li>You champion ethical conduct, accountability, and a winning team culture.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required; advanced degree or certification preferred.</li><li>Minimum 5 years of sales leadership or management in oncology or hematology.</li><li>Proven success hiring, coaching, developing, promoting, and retaining top talent.</li><li>Strong record of sales performance with high integrity and accountability.</li><li>Experience developing account plans and implementing commercial strategies.</li><li>Proficiency with sales data, analytics, and customer relationship management systems.</li><li>Strong collaboration, leadership, interpersonal, communication, presentation, planning, and prioritization skills.</li><li>Ability to build deep customer relationships and organizational credibility.</li><li>Ability and willingness to travel 30-40%, including some weekends.</li><li>Fluent Japanese language skills.</li><li>Hematology or biologics experience preferred.</li><li>Intermediate English language skills preferred.</li><li>Highest personal values and ethical standards.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, AI Portfolio, Value Realization, Strategy & Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49698]]></requisitionid>
    <referencenumber><![CDATA[R49698]]></referencenumber>
    <apijobid><![CDATA[r49698]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49698/executive-director-ai-portfolio-value-realization-strategy-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're looking for an Executive Director, Portfolio, Value Realization, Strategy & Ops to join our fast-moving Enterprise Data & AI organization. You'll act as the internal strategist and investment steward for our enterprise AI and data agenda, owning the roadmap, investment prioritization, and ROI tracking that ensures every AI dollar delivers measurable value. You'll serve as the key connector between the AI portfolio and executive stakeholders, telling a clear story of where we're investing, what it's returning, and what comes next. This role reports to the SVP, Chief AI Officer, and offers the chance to shape how a science-driven company invests in its AI future.</p><p><strong>When & where:</strong></p><ul><li><strong>Location:</strong> This role is open to any of our Tri-State locations: Sleepy Hollow, NY, Tarrytown, NY, Armonk, NY, Warren, NJ or Cambridge, MA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Own the enterprise AI and data roadmap, turning business and scientific priorities into a sequenced, well-justified portfolio</li><li>Lead planning and review processes for the Enterprise Data & AI organization, including annual planning and quarterly reviews</li><li>Manage AI and data initiatives as a disciplined investment portfolio, with clear sponsors and outcomes for each</li><li>Build and run a value realization framework that ties every AI initiative to a measurable business result</li><li>Set enterprise strategy for generative AI tools, including buy, license, or build decisions and total cost modeling</li><li>Lead the enterprise AI product management function, including roadmaps and adoption accountability</li><li>Manage vendor relationships across the AI tools landscape, including negotiations and performance tracking</li><li>Serve as the main point of contact for executive stakeholders on AI strategy, performance, and investment decisions</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have a track record of connecting technology investment to measurable business results</li><li>Enjoy building frameworks and processes from the ground up</li><li>Bring strong strategic and financial thinking, including modeling trade-offs and building ROI frameworks</li><li>Stay current on the AI landscape, including generative AI, agentic systems, and enterprise AI platforms</li><li>Know how to build product management practices for AI capabilities</li><li>Can influence and build trust across a matrixed organization without relying on formal authority</li><li>Bring genuine curiosity about how AI is transforming drug discovery and clinical development</li><li>Enjoy developing and growing strategy and product talent</li></ul><p><strong>This role requires:</strong></p><ul><li>A Bachelor's degree in a related field (advanced degree required for certain scientific or clinical positions)</li><li>17+ years of experience in enterprise strategy, portfolio management, or AI/data leadership</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Specialist Indirect Procurement]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48243]]></requisitionid>
    <referencenumber><![CDATA[R48243]]></referencenumber>
    <apijobid><![CDATA[r48243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48243/sr-specialist-indirect-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist Category Management Indirect Procurement to join our Global Procurement team, supporting our Indirect Procurement categories in a hybrid work model. In this role, you will support category strategy development, sourcing activities, supplier relationship management, category analytics, and procurement process improvement while collaborating with Category Leads, Procurement colleagues, partners, and suppliers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Support the Manager, Category Management and Category Lead in implementing category strategies across Professional Services, including Law, Finance, Consulting, and HR Services categories.</p></li><li><p>Prepare category intelligence, market research, supplier benchmarking, and analytical insights to support category strategy development and partner engagement.</p></li><li><p>Assist sourcing activities by preparing Requests for Information (RFI), Requests for Quotation (RFQ), and Requests for Proposal (RFP), conducting bid analyses, and evaluating supplier responses.</p></li><li><p>Summarize sourcing and supplier relationship management outcomes through comparative analysis of supplier responses, pricing, and evaluations to support decision-making.</p></li><li><p>Maintain category plans, opportunity analyses, supplier relationship management materials, and procurement documentation within the central repository.</p></li><li><p>Contribute to process improvement initiatives, compliance reviews, audit support activities, and enhancements to procurement policies, templates, and training materials.</p></li><li><p>Support tail spend management, category refresh reviews, supplier validation checks, and category development initiatives using internal and external data sources.</p></li><li><p>Demonstrate responsiveness and accountability by managing category requests, providing timely updates, and raising issues when needed to support service delivery standards.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field of study and experience in procurement; experience within Pharma or BioPharma preferred.</p></li><li><p>Working knowledge of category management principles, including sourcing, procurement, planning, supplier interactions, and negotiations.</p></li><li><p>Working knowledge of Enterprise Resource Planning (ERP) systems such as Oracle.</p></li><li><p>Experience with Source-to-Pay (S2P) platforms such as Oracle, Zycus, GEP, Ariba, or similar platforms preferred.</p></li><li><p>Experience with ServiceNow and iCertis or similar contract lifecycle management platforms preferred.</p></li><li><p>Proficiency in Word, Excel, and PowerPoint for communication, presentations, and data analysis.</p></li><li><p>Experience with spend analytics software preferred.</p></li><li><p>Excellent written and verbal English communication skills.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44896]]></requisitionid>
    <referencenumber><![CDATA[R44896]]></referencenumber>
    <apijobid><![CDATA[r44896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44896/principal-statistical-programmer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: onsite</li><li></li></ul><p><strong>Discover your role:</strong></p><ul><li>Support or lead programming and quality control of analysis datasets, tables, listings, and graphs</li><li>Coordinate activities and communicate shifting timelines and milestones to the study team</li><li>Create and maintain programming specifications for analysis datasets across studies</li><li>Support creation and validation of submission requirements, including annotated CRFs and define documents</li><li>Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch</li><li>Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed</li><li>Participate in department working groups, contributing to tool development and process improvement</li><li>Design and test program logic independently, maintaining documentation in a regulated environment</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Enjoy working independently while staying closely connected to a broader study team</li><li>Communicate clearly and proactively, especially around shifting timelines</li><li>Take pride in accuracy and consistency when documenting and maintaining code</li><li>Think analytically and enjoy solving programming and data challenges</li><li>Stay curious about process improvement and enjoy contributing ideas to working groups</li><li>Adapt comfortably to ad hoc requests and evolving priorities from senior leadership</li><li>Bring attention to detail and a quality mindset to regulated work</li></ul><p><strong>This role requires:</strong></p><ul><li>Master's degree with 3+ years of relevant experience</li><li>Proven programming experience supporting clinical study data and analysis deliverables</li><li>Strong documentation and quality control skills within a regulated environment</li><li>Experience collaborating within a multidisciplinary study team</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Process Specialist, Fill Finish Manufacturing]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47994]]></requisitionid>
    <referencenumber><![CDATA[R47994]]></referencenumber>
    <apijobid><![CDATA[r47994]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47994/staff-process-specialist-fill-finish-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Process Specialist — Manufacturing (Principal, Staff, or Senior Staff) to join our IOPS team, providing on-the-floor technical direction and leadership across our biopharmaceutical manufacturing process. In this role, you will resolve process challenges, coach manufacturing personnel, lead investigations, and drive continuous improvement — while collaborating with Process Science, Engineering, Quality, Regulatory, and Facilities teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Provide on-the-floor technical input to resolve process problems, coach manufacturing personnel on critical process steps, and support implementation of process and work system improvements in the production suites</li><li>Lead investigations into process variances, support CAPA implementation, and guide validation activities involving manufacturing equipment and processes</li><li>Support technology transfer of the manufacturing process, liaising with process science and technology transfer teams on transfer and startup activities</li><li>Track, trend, and present relevant technical and business process metrics; prepare reports by collecting and analyzing information for review with the Process Science Group</li><li>Write, review, and approve SOPs, specifications, regulatory filings, and other controlled documents; perform cGMP audits and represent Manufacturing during regulatory and client audits</li><li>Act as system owner for defined manufacturing equipment, coordinating all non-routine activities and ensuring policies and procedures comply with regulatory requirements</li><li>Lead and implement continuous improvement initiatives; support safety improvements requiring technical and engineering input</li><li>Interface cross-functionally with Facilities, Process Development, Engineering, Process Analytical Sciences, Regulatory, Quality Assurance, and Quality Control</li><li>Knowledge of cGMP manufacturing and familiarity with formulation, aseptic filling, visual inspection, assembly, labeling, and/or packaging of liquid and lyophilized injectable products</li><li>Technology transfer and equipment and process validation experience in aseptic parenteral fill/finish operations preferred</li><li>Experience with lyophilization a plus; experience operating and qualifying highly automated equipment a plus</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>BS in Life Sciences or a related field</li><li>Principal Process Specialist: 8+ years of relevant cGMP manufacturing, engineering, or scientific experience</li><li>Staff Process Specialist: 10+ years of relevant cGMP manufacturing, engineering, or scientific experience</li><li>Senior Staff Process Specialist: 12+ years of relevant cGMP manufacturing, engineering, or scientific experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Public Policy - Science and Food and Drug Administration Policy]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47412]]></requisitionid>
    <referencenumber><![CDATA[R47412]]></referencenumber>
    <apijobid><![CDATA[r47412]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47412/director-public-policy-science-and-food-and-drug-administration-policy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Washington]]></city>
    <state><![CDATA[District of Columbia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Director of Policy & Government Affairs – Science and Food and Drug Administration (FDA) Policy will lead Regeneron’s science and FDA policy portfolio, developing, shaping and influencing government and multinational organization policy related to the scientific research and development of biopharmaceutical medicine and cell and gene therapy across the product lifecycle. Relevant issues include but are not limited to product approval standards and pathways, scientific ethics and integrity, clinical trial activity, evidence development, manufacturing and CMC criteria, and biosimilars. Although US-focused, the position may also support the ex-US Public Policy & Government Affairs lead on key science and biotechnology medicine policy around the world as needed.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Washington, D.C.</p></li><li><p>Hybrid: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage with internal subject matter experts and leaders to understand Regeneron’s business and corporate interests, recognize policy risks and opportunities, and determine short and long-term policy objectives in order to navigate and balance competing interests and objectives</p></li><li><p>Communicate Regeneron's policy positions and initiatives to internal and external audiences through various channels;</p></li><li><p>In collaboration with relevant internal team members, organize and participate in events, conferences, and forums to promote Regeneron's policy agenda;</p></li><li><p>As needed, represent the Regeneron PP&GA team at key stakeholder meetings and engage with key external partners at meetings to identify opportunities for collaboration to advance common policy priorities.</p></li><li><p>Engage with industry associations, advocacy groups, and other external stakeholders in collaboration with the alliance development lead to build coalitions and advance shared policy objectives</p></li><li><p>Develop and advance strategic public policy positions and initiatives that align with and advance Regeneron's business objectives;</p></li><li><p>Monitor and analyze legislative and regulatory developments at the federal, state, local, and international levels to determine the potential impact on and importance to Regeneron;</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree is required; advanced degree/s in Public Policy, Political Science, Law, or related field and science background strongly preferred.</p></li><li><p>Minimum of 12 years of relevant experience in science and regulatory policy, preferably with substantial experience at the US FDA</p></li><li><p>Proven record of successfully crafting and influencing public policy and navigating complex and highly technical issues</p></li><li><p>Strong understanding of the biopharmaceutical industry, including regulatory and legislative processes</p></li><li><p>Develop and execute strategic advocacy plans, including proactively crafting and vetting legislative and regulatory proposals to advance company priorities and mitigate risks;</p></li><li><p>Provide expert advice and guidance on policy and regulatory matters to internal stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager - Hematology (f/m/d) - Germany South-East]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49848]]></requisitionid>
    <referencenumber><![CDATA[R49848]]></referencenumber>
    <apijobid><![CDATA[r49848]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49848/key-account-manager-hematology-fmd-germany-south-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hematology to join our International Hematology team, supporting Germany in a field-based work mode. In this role, you will drive account performance and regional contracting activities for our hematology portfolio while collaborating with Medical colleagues, pharmacists, hospital stakeholders, and commercial teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Field-based in Germany South-East</p><p><strong>Discover your role:</strong></p><ul><li><p>Establish high-quality healthcare professional relationships across the territory</p></li><li><p>Develop referral networks spanning hospital, outpatient, and office-based settings</p></li><li><p>Deliver portfolio value messages through face-to-face, remote, and digital engagement</p></li><li><p>Partner with Medical on regional programs and healthcare professional activities</p></li><li><p>Manage account planning, segmentation, targeting, and local account plans</p></li><li><p>Support regional contracting activities and adapt contract models to local needs</p></li><li><p>Analyze market trends and competitor activity to inform negotiations</p></li><li><p>Thrive in an agile environment and adjust priorities to account needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or recognized equivalent for sales professionals</p></li><li><p>5-7 years of progressive pharmaceutical or biotechnology sales experience</p></li><li><p>Knowledge of the German healthcare system and regional market structures</p></li><li><p>Experience using data, customer relationship management systems, and multiple business systems</p></li><li><p>Qualification in applicable pharmaceutical industry codes, including EFPIA Code or VFA Pharmakodex</p></li><li><p>Fluency in German and good working knowledge of English</p></li><li><p>Ability to manage a large territory independently with frequent travel</p></li><li><p>Strong customer engagement, negotiation, and communication skills</p></li><li><p>High integrity and ethical standards in all interactions</p></li><li><p>Hematology sales experience and an established network strongly preferred</p></li><li><p>Experience supporting hospital, purchasing group, or payer contract negotiations preferred</p></li><li><p>Product launch experience preferred</p></li></ul><p>Salary range (annually)</p><p>73,125 -121,875 €</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Market Access Analytics - Neurology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46822]]></requisitionid>
    <referencenumber><![CDATA[R46822]]></referencenumber>
    <apijobid><![CDATA[r46822]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46822/associate-director-market-access-analytics-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director</strong> to join our <strong>Market Access Analytics, Neurology</strong> team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><p>This is a hands-on analytics role responsible for transforming complex data assets and advanced analytical tools into evidence-based market access decisions across Payer & Provider/GPO, Contracting, and Pricing. The Associate Director will lead the design, curation, and evaluation of market access data - translating it into strategic analytical solutions that sharpen payer and channel strategy, optimize provider and GPO contracting, and drive portfolio performance.</p><p><em>Lead </em></p><p>1) Shape payer and channel strategy by synthesizing market, payer, and account-level data to inform strategic positioning, coverage decisions, and channel optimization across the portfolio.</p><p>2) Drive payer segmentation and policy analytics across Commercial, Medicare Part B/D, Medicare Advantage, Managed Medicaid, FFS Medicaid, VA/DoD, and Exchange segments - integrating intelligence on Payer willingness and ability to manage drug utilization to surface actionable insight.</p><p><em>Partnership and Collaboration </em></p><p> 3) Build strong, productive relationships with cross-functional stakeholders across Market Access Strategy, Payer Account teams, GPO Account Directors, and Brand colleagues - balancing analytical rigor, timelines, and influence to drive aligned outcomes.</p><p>4) Serve as a strategic thought partner by sharpening business questions, structuring analyses, and translating complex findings into clear, compelling recommendations for senior leadership.</p><p><em>Develop </em></p><p>5) Proactively identify emerging analytics opportunities that address critical market access challenges and unlock growth across the portfolio.</p><p>6) Advance measurement frameworks to evaluate pre- and post-performance across Payer and GPO initiatives, enabling continuous strategic improvement.</p><p>7) Deliver provider and GPO analytics - including account- and segment-level opportunity assessments and pull-through analysis tied to recent payer coverage or brand-level developments.</p><p><em>Execute </em></p><p>8) Serve as the day-to-day analytics partner to Market Access Strategy, HEOR, Pricing, Trade, GPO, and Field Reimbursement teams - scoping questions, executing analyses, and delivering actionable insights on time.</p><p>9) Lead performance reporting tied to strategic imperatives and priority business questions, ensuring clarity, consistency, and alignment across stakeholders.</p><p>10) Triangulate across diverse datasets to surface and deliver actionable insights that uncover opportunities and portfolio-level strategies.</p><p>11) Manage analytics vendor workstreams from scoping through delivery - defining deliverables, maintaining rigor, and driving timely execution.</p><p>12) Apply Regeneron's proprietary Market Access semantic layer across key third-party data sources - including payer medical policy, patient-level claims, and reimbursement data - to ensure analytical consistency and depth.</p><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10 years of pharmaceutical/biotech commercial experience (or 7+ years for MBA/MS), in roles of increasing accountability; prior experience with market-leading brands is desired.</p></li><li><p>BS/BA in STEM related field, e.g., Statistics, Econometrics, Mathematics, Business Analytics; Advanced degree preferred. </p></li><li><p>Proficiency across key market access data sources — MMIT, IQVIA LAAD/DDD/Xponent, Remittance, Model N, Integrichain 852/867, and Patient HUB — with working knowledge of Payer spine bridge files and account hierarchy.</p></li><li><p>Experience coding in Python, R and/or SQL. </p></li><li><p>Experience in data visualization and commercial business intelligence tools required (e.g., Dataiku, Databricks, PowerBI, Tableau, QlikView, Oracle BI, Microstrategy, Cognos, Spotfire or similar tools). </p></li><li><p>Expertise in data visualization and data storytelling of key findings. </p></li><li><p>Advanced proficiency in Excel, and PowerPoint required. </p></li><li><p>Experience in data mining, descriptive analytics, application of statistical methods, analyses and modeling, predictive modeling, opportunity assessment and quantification. </p></li><li><p>Proven track record of managing multiple external vendors and project teams concurrently against stringent deadlines in a fast-paced, timeline-driven atmosphere. </p></li><li><p>Communication and influencing skills with demonstrated ability to succinctly and effectively present compelling reviews of analyses that integrate analytics and patient journey implications/actions to be taken. </p></li><li><p>Strong analytical skills and strategic thinking ability. </p></li><li><p>Concise and impactful written and verbal communication skills with demonstrated experience in influencing and driving decision making. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48142]]></requisitionid>
    <referencenumber><![CDATA[R48142]]></referencenumber>
    <apijobid><![CDATA[r48142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48142/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA</p></li><li><p>4 days per week onsite</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 13 Aug 2026 00:59:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Systems & Collaboration Platforms Business Operations]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49917]]></requisitionid>
    <referencenumber><![CDATA[R49917]]></referencenumber>
    <apijobid><![CDATA[r49917]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49917/senior-manager-systems-collaboration-platforms-business-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Senior Manager, Systems & Collaboration Platforms Business Operations serves as the business-side operational owner for Enterprise Planning and Collaboration Platforms, including Planisware, Planview Advisor, Microsoft 365 collaboration platforms, and related enterprise systems. This role is responsible for supporting effective platform operations, governance, business administration, user support, and operational readiness across the enterprise.</p><p>Reporting to the Director, Enterprise Planning & Collaborations Platforms, this position partners closely with Regeneron Digital & Technology, Enterprise Stewardship & Standards, Data Stewardship & Quality, DADS, Business Process Owners, and Functional Area subject matter experts across the enterprise to ensure platforms operate efficiently, support business objectives, and remain aligned with governance standards and operational requirements. The role owns platform operations and business administration while working within established data governance frameworks and stewardship processes.</p><br><h3>When & where:</h3><ul><li>Location: Tarrytown, NY or Warren, NJ</li></ul><br><h3>Discover your role:</h3><ul><li>Execute operational priorities established by the Enterprise Planning & Collaborations Platforms Lead, ensuring day to day administration, platform performance & reliability, operational effectiveness, and user readiness across Enterprise Planning and Collaboration Platforms.</li><li>Serve as the business-side owner for platform operations, partnering with Regeneron-Digital & Technology to support system administration/product owner activities, user access management, incident resolution, system upgrades, releases, and operational support.</li><li>Manage business administration processes, including access approvals, user onboarding, operational support, issue intake, and request tracking.</li><li>Coordinate User Acceptance Testing (UAT) activities for system enhancements and releases, ensuring business readiness, stakeholder engagement, and effective issue resolution.</li><li>Establish and maintain operational standards, service processes, governance documentation, knowledge articles, and business-rule documentation to support compliance, audit readiness, and consistent platform use.</li><li>Prepare decision records, impact assessments, recommendations, and escalation packages to support governance forums and operational decision-making.</li><li>Partner with stakeholders across the enterprise, including Enterprise Stewardship & Standards, Data Stewardship & Quality, DADS, Regeneron-Digital & Technology, Business Process Owners, and Functional Area leaders, to ensure platform operations, governance processes, reporting readiness, and business requirements remain aligned with enterprise standards and strategic objectives.</li><li>Support governance and change-control processes by evaluating operational impacts, maintaining documentation, and facilitating implementation of approved changes.</li><li>Monitor and report key operational metrics, including user satisfaction, issue resolution performance, change success rates, platform adoption, and compliance with approved standards.</li><li>Identify and implement opportunities to improve user experience, platform effectiveness, operational efficiency, and governance maturity across the enterprise platform ecosystem.</li><li>Support functional SMEs, Change Agents, and business stakeholders by providing operational guidance, responding to platform-related inquiries, and ensuring user needs are represented in platform decisions.</li><li>Maintain operational records, documentation, and knowledge repositories to support compliance, transparency, and business continuity.</li></ul><br><h3>This role requires:</h3><ul><li>Minimum of a Bachelors degree and 8+ years in operational or enterprise planning, including experience facilitating cross-functional alignment on processes and initiatives. Biopharma / drug development experience preferred.</li><li>Experience supporting enterprise planning, portfolio management, project management, resource management, or collaboration platforms in a biopharma, R&D, or regulated business environment.</li><li>Experience with Planisware, Planview Advisor, Microsoft 365, SharePoint, Power Platform, Power BI, or similar business operations and workflow platforms.</li><li>Experience developing or maintaining business-rule documentation, knowledge articles, UAT materials, operational SOPs, decision records, or governance documentation.</li><li>Experience supporting platform governance, change control boards, release management, access governance, template governance, or operational support models.</li><li>Familiarity with data stewardship, data governance, analytics/reporting, and enterprise glossary concepts is preferred, particularly to support partnership with Enterprise Stewardship & Standards.</li><li>Experience tracking adoption, user engagement, operational metrics, support trends, and service performance indicators.</li></ul><br><h3>Preferred Qualifications:</h3><ul><li>PMI Project Management Professional (PMP) is preferred but not required.</li><li>Demonstrated success leading cross-functional initiatives and influencing stakeholders across a complex matrix organization</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 18 Aug 2026 18:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Sciences]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50144]]></requisitionid>
    <referencenumber><![CDATA[R50144]]></referencenumber>
    <apijobid><![CDATA[r50144]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50144/senior-manager-clinical-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Sciences to join our Global Capability Center (GCC) in Hyderabad. In this role, you will lead and manage a centralized pool of Clinical Data Reviewers (CDRs) and Medical Narrative Reviewers (MNRs), ensuring high-quality clinical review support across the development portfolio. You will oversee onboarding, training, performance management, resource allocation, capacity planning, and operational excellence while partnering closely with Clinical Scientists, Medical Directors, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Hyderabad (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li>Lead the day-to-day functional management of a centralized pool of Clinical Data Reviewers and Medical Narrative Reviewers, serving as the primary point of contact for resource coordination across studies and programs.</li><li>Translate portfolio-level study assignments into resource prioritization plans and monitor delivery against achievements and key operational objectives.</li><li>Personally perform clinical data review, query management, and medical narrative review activities when required to support coverage gaps, onboarding periods, workload surges, or quality remediation initiatives.</li><li>Establish, monitor, and report key performance indicators (KPIs), ensuring compliance with SOPs, Restricted Data Handling requirements, and quality standards.</li><li>Lead onboarding and training activities, including SOP assignment, systems access support, and reviewer readiness assessments in partnership with Clinical Scientists and Study Medical Directors.</li><li>Drive capacity forecasting and workforce planning activities by collaborating with Clinical Scientist Leads and Clinical Program Leads to align resources with study timelines and business needs.</li><li>Ensure continuity of governance and operational excellence during team transitions, turnover, protocol changes, and study closeouts.</li><li>Support knowledge management, institutional learning, and consistency of reviewer practices across the portfolio.</li><li>Represent the Clinical Sciences function within the GCC and contribute to strategic initiatives focused on quality, efficiency, and process improvement.</li></ul><p><strong>This role requires:</strong></p><ul><li>Advanced degree in a scientific or medical field; MD, PhD, PharmD, or equivalent strongly preferred.</li><li>Minimum 7 years of experience in clinical research, drug development, pharmaceutical operations, or related healthcare industry environments.</li><li>Hands-on experience performing clinical data review and/or medical review of patient narratives.</li><li>Practitioner-level knowledge of EDC systems, clinical data review tools, query management processes, and narrative review activities.</li><li>Demonstrated experience managing, coaching, and developing clinical and medical professionals within a matrixed and cross-functional environment.</li><li>Strong operational leadership, quality governance, and stakeholder management capabilities.</li><li>Excellent communication, collaboration, and interpersonal skills with the ability to influence and lead distributed teams.</li><li>Strong analytical, critical thinking, and problem-solving abilities.</li><li>Scientific and medical competence to understand, evaluate, and communicate complex clinical development concepts.</li><li>Willingness to perform hands-on review activities as needed to ensure quality, continuity, and timely delivery.</li><li>High level of integrity, professionalism, and discretion when handling sensitive information.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 19 Aug 2026 06:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Key Accounts Marketing]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50073]]></requisitionid>
    <referencenumber><![CDATA[R50073]]></referencenumber>
    <apijobid><![CDATA[r50073]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50073/director-key-accounts-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>This role of Director, Oncology Key Accounts Marketing will be responsible for supporting our vision for best-in-class capabilities and innovative solutions to support engaging Oncology and Hematology Key Strategic Provider Accounts.</p><p>This candidate facilitates development of, any updates to our Provider Key Account Strategy for our Commercial Business Unit. In this role, will develop Key Account Marketing sponsorships strategy aligned to annual brand plan plus content and executes rollout to the Oncology Key Account Leader (OKAL) team focused on building loyalty with customers and ensures our Oncology brand(s) resonate with stakeholders and C-Suite and D-Suite leaders in key oncology accounts in the US. This individual will report to the Global Core Brand Lead.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY Office - 4 days a week</li><li>Travel up to 30% of the time</li></ul><h3>Discover your role:</h3><ul><li>Develop promotional strategy and tactical plan as well as develop all tactics for OKAL use with Key acct/VA targets aligned to the brand plan including approval through RC</li><li>Partner with brand marketing teams to develop deep understanding of indication and overall brand strategy and US tactical focus, as well as share data and insights Key Accts Performance to inform marketing plans across the brand.</li><li>Work closely with OKAL Leader and OKALs as a dotted line member of the OKAL Leadership Team, attending regular OKAL team calls and meetings, and attend professional association meetings to connect regularly with OKAL target customers/partners</li><li>Provide leadership support to the development of the overall Brand Plan and strategy focusing on key accounts.</li><li>Ensure innovative solutions and procedures are demonstrated for reaching OKAL Acct based partners, C-Suite and acct operational leadership, developing collaborative projects as agreed upon with OKAL Sr Director and Head of Marketing</li><li>Understand and leverage trends in the marketplace and competitive benchmarking to inform strategies for key acct engagement.</li><li>Actively collaborate and provide additional support to OKAL Sr Director and OKAL team operations work e.g. targeting, performance reporting, and business planning/presentations</li><li>Manage the Key Accounts Marketing budget, ensure cost effective delivery of all programs while tracking and monitoring effectiveness including KPI’s, ROI and actionable findings.</li></ul><h3>This role requires:</h3><ul><li>At least 12 years of progressive experience in the pharmaceutical or biotech industry, with significant leadership experience in marketing, sales, and sales management in oncology preferred. At least 5 years in a marketing role.</li><li>A bachelor’s degree Required, MBA preferred.</li><li>Demonstrated competency in marketing innovation including managing ad agencies/vendors, and marketing strategy and tactical effectiveness measures</li><li>Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate.</li><li>Proven track record of market analysis and identifying growth opportunities.</li><li>Ability to synthesize inputs from external and internal collaborators such as HCPs, field teams, and market access colleagues.</li><li>Effective written and oral communication; experience delivering complex messages to diverse internal and external collaborators with a track record of influential presentations.</li><li>Ability to communicate and act promptly; demonstrated initiative and creativity; and the agility to work effectively in complex, rapidly changing environments.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Cell Therapy]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49309]]></requisitionid>
    <referencenumber><![CDATA[R49309]]></referencenumber>
    <apijobid><![CDATA[r49309]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49309/senior-medical-director-clinical-development-cell-therapy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Hematology team supporting Cell Therapy Clinical Development. In this role, you will provide clinical leadership and responsibility for all clinical deliverables within an assigned section of a clinical program in Hematology/Oncology, operating with minimal supervision from the Program Lead MD. Clinical deliverables may include individual protocols consistent with the Clinical Development Plan (CDP), clinical components of regulatory documents and registration dossiers, brand-related medical information, and clinical communications and publications. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference for patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Travel: 10%, to relevant congresses and conferences</p></li></ul><h3><strong>Discover your role:</strong></h3><ul><li><p>Manage all operational aspects and drive execution of clinical programs, in partnership with global line functions, the assigned Clinical Scientist, and Clinical Operations associates, to ensure timely execution of assigned clinical deliverables within approved budget.</p></li><li><p>Lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, Health Economics & Outcomes Research [HE&OR]), as well as internal decision boards.</p></li><li><p>Ensure the overall safety of the compound in collaboration with the Safety Lead for the assigned program</p></li><li><p>Lead development of clinical sections of program-level regulatory documents, such as Investigators' Brochures, briefing books, safety updates, and IND/NDA (Investigational New Drug/New Drug Application) submission documents, and lead responses to Health Authority questions</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>A M.D. or equivalent medical degree (e.g., D.O., MBBS), preferably with clinical training in a relevant disease area such as Hematology or Oncology.</p></li><li><p>Significant demonstrated experience of 4+ years in clinical research within an industry environment, spanning clinical activities across Phases 1 through 4. Cell Therapy experience preferred.</p></li><li><p>Strong understanding of the global regulatory environment, including key regulatory agencies and approval processes.</p></li><li><p>Strong understanding of the operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out).</p></li><li><p>People management experience preferred but not required.</p></li></ul><p>#MDJobs #MDJobsCD #GDTherapeuticJobs #Hematology #CellTherapy</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 14 Aug 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate CMC Product Quality Compliance Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49210]]></requisitionid>
    <referencenumber><![CDATA[R49210]]></referencenumber>
    <apijobid><![CDATA[r49210]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49210/associate-cmc-product-quality-compliance-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing</p><p>medicines for people with serious diseases. Regeneron is currently seeking an <strong>Associate CMC Product Quality Compliance Specialist</strong> to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Overseeing the global change management implementation plan.</p></li><li><p>Supporting the evaluation of impact of proposed process changes, deviations and CAPAs on the end-to-end supply chain.</p></li><li><p>Overseeing the coordination and generation of the annual PQRs and yearly biologic product reports (YBPR).</p></li><li><p>Assessing quality-related information to detect trends and work with subject matter experts to determine the need for actions required in response to those trends.</p></li><li><p>Ensuring the drug supply distribution compliance with all aspects of global regulatory filings to ensure stable supply positioning.</p></li><li><p>Interacting with global regulatory authorities in support of the CMC activities during Agency inspections.</p></li><li><p>Executing relationship management with other areas of Regulatory, Quality, Manufacturing, and Supply organizations to support product distribution.</p></li><li><p>Developing procedures and systems for enhanced tracking of change controls and global regulatory submissions/approvals.</p></li><li><p>Supporting launch readiness and distribution compliance through ensuring appropriate GMP source documentation is in place to support regulatory activities and launch material is aligned with the applicable regulatory dossiers.</p></li><li><p>Providing writing and strategy support in communications to regulatory agencies including product deviation reports (BPDR, QDR, PDR, etc.), clinical notice of events and agency inspection responses in collaboration with CMC RA, QA, and SMEs as applicable.</p></li><li><p>Facilitating the commercial and registration requests (CARRs) process in collaboration with CMC PM, CMC RA, IMT and SMEs as applicable.</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have excellent interpersonal skills.</p></li><li><p>You demonstrate a strong quality mindset.</p></li><li><p>You have strong analytical and organizational skills.</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p><strong>Assoc Specialist:</strong> Requires BS/BA in Chemistry, Biology, or related field, with relevant experience or equivalent combination of education and experience, preferably pharmaceutical or medical device, including some supervisory and/or leadership experience.</p></li><li><p><strong>Specialist: </strong>Requires BS/BA in Chemistry, Biology, or related field, with 2+ years of relevant experience in pharmaceutical or medical device, including some supervisory and/or leadership experience or equivalent combination of education and experience.</p></li><li><p><strong>Sr Specialist</strong>: Requires BS/BA in Chemistry, Biology, or related field, with 5+ years of relevant experience in pharmaceutical or medical device, including some supervisory and/or leadership experience or equivalent combination of education and experience.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €59,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Quality Assurance Reviewer]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48353]]></requisitionid>
    <referencenumber><![CDATA[R48353]]></referencenumber>
    <apijobid><![CDATA[r48353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r48353/principal-quality-assurance-reviewer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Quality Assurance (QA) Specialist/Reviewer to support our Fill Finish facility. In this role, you will perform all compliance related tasks necessary to review and approve investigations and provide quality oversight to the implementation of robust corrective actions for supporting manufacturing operations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Independently reviews and approves:</p><ul><li><p>Investigations into non-conformances and proposed actions to prevent reoccurrences in support of manufacturing operations</p></li><li><p>Laboratory investigations into out of specification (OOS) and out of trend ( OOT) results</p></li><li><p>Supplier corrective action requests and proposed vendor actions</p></li></ul></li><li><p>Coaches investigation team to enable preparation of investigation reports that include recommendations on investigation findings for medium/high severity non-conformances</p></li><li><p>Analyzes and evaluates information captured through investigations, summarizes information and trends in investigation reports</p></li><li><p>Presents quality considerations and recommendations at group meetings with multiple levels of management</p></li><li><p>Reviews primary data sources to assure the accuracy of investigative conclusions in accordance with cGMP standards in support of investigations</p></li><li><p>Provides quality reviews and oversight on a wide range of investigations of differing subject matter</p></li><li><p>Monitors production processes and quality systems data to acquire vital data in support of investigations and track efficiency of changes</p></li><li><p>Participates in and/or leads cross-functional study teams to get results</p></li><li><p>Captures, trends and analyzes process related data to drive consistency and timeliness</p></li><li><p>Trains employees on investigative processes and techniques</p></li><li><p>Coordinates and/or leads cross-functional meetings with multiple departments</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in Life Sciences, Engineering or related field; or equivalent combination of education and experience</p><ul><li><p>Principal QA Specialist: 8+ years of relevant experience</p></li><li><p>Staff QA Specialist: 10+ years of relevant experience</p></li><li><p>Level will be determined based on experience</p></li></ul></li><li><p>Experience with sterile drug product manufacturing, fill finish and/or quality control testing</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 17 Aug 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Associate]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49892]]></requisitionid>
    <referencenumber><![CDATA[R49892]]></referencenumber>
    <apijobid><![CDATA[r49892]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r49892/automation-associate/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. The Bioanalytical Sciences (BAS) Automation group at Regeneron is seeking a Laboratory Automation Associate. This position will contribute to the development, implementation, and maintenance of laboratory automation solutions within BAS. In this role, you will work with automation technologies used to streamline bioanalytical laboratory workflows, support automated assay development, and help ensure reliable and efficient laboratory operations.</p><p><strong>When & where:</strong></p><p>Location: Tarrytown, NY (On-site)</p><p><strong>Discover your role:</strong></p><ul><li><p>Working with integrated laboratory automation systems, including liquid handlers and automated laboratory instrumentation in a regulated environment</p></li><li><p>Collaborating with automation engineers and laboratory scientists to develop, implement, and troubleshoot automated workflows for laboratory processes</p></li><li><p>Developing and updating programs for automation systems, including debugging scripts, performing test runs, and supporting process optimization activities</p></li><li><p>Performing manual and automated experiments to support assay development, troubleshooting, and automated process investigations</p></li><li><p>Providing technical support and guidance to end users on the operation and maintenance of automation systems and laboratory instrumentation</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p> A Bachelor's degree in a scientific or engineering field</p></li><li><p>0–3 years of relevant industry experience in a laboratory environment</p></li><li><p>Basic programming knowledge or experience</p></li><li><p>Basic knowledge or experience with laboratory instrumentation</p></li><li><p>Enjoyment of troubleshooting technical challenges and identifying practical solutions</p></li><li><p>Strong problem-solving skills and a detail-oriented mindset</p></li><li><p>The ability to effectively communicate and collaborate with cross-functional teams</p></li><li><p>An interest in laboratory automation and learning new technologies</p></li><li><p>Experience operating liquid handling instruments (e.g., Tecan, Hamilton, Lynx, or similar platforms) and knowledge of integrated systems is preferred </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 20 Aug 2026 13:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[PharmD Program Associate - Safety Sciences]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50230]]></requisitionid>
    <referencenumber><![CDATA[R50230]]></referencenumber>
    <apijobid><![CDATA[r50230]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50230/pharmd-program-associate-safety-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> </p><p>The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles. </p><p>This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. </p><p><strong>When & where:</strong> </p><ul><li><p><strong>Location:</strong> Tarrytown, NY </p></li><li><p><strong>Travel percentage:</strong> Up to 15% </p></li></ul><p><strong>Program Tracks:</strong> <br>The program is comprised of a 24-month rotational experience within one of the following tracks: </p><ul><li><p>Clinical Operations & Program Management </p></li><li><p>Clinical Sciences </p></li><li><p>Regulatory Strategy </p></li><li><p>Regulatory Labeling & Advertising/Promotion </p></li><li><p><strong>Safety Sciences</strong> </p></li></ul><p>Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program. </p><p><strong>Safety Sciences </strong>– Associate will gain a working knowledge of various pharmacovigilance (PV) disciplines that enable the continuous assessment of the benefit-risk of Regeneron products throughout the product life cycle, from early clinical development through market authorization and including post marketing surveillance, with a focus on signal detection and management. The Associate will build foundational knowledge and experience in case processing operations and will gain an understanding of various PV business support functions enabling a global pharmacovigilance organization, while also having the opportunity to interface cross-functionally on tasks/projects.</p><p><strong>Discover your role:</strong> </p><ul><li><p>Drafting documents integral to clinical sites and regulatory submissions </p></li><li><p>Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others </p></li><li><p>Managing third-party vendors and maintaining timelines of key results </p></li><li><p>Developing regulatory strategies for clinical development programs </p></li><li><p>Analyzing safety data to characterize the safety profile of products throughout their development lifecycle </p></li><li><p>Working with program mentors to improve skills to reach professional goals better </p></li><li><p>Opportunities to travel to clinical sites and/or meetings with health authorities </p></li></ul><p><strong>This role requires:</strong> </p><ul><li><p>Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates within a life science related area of study may also be considered. </p></li><li><p>You must have completed your PharmD and/or PhD degree by Summer 2027 </p></li><li><p>Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus </p></li><li><p>Exposure or familiarity with evaluating clinical trials, scientific literature and data </p></li><li><p>You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences You are eligible to work in the U.S. on a permanent basis </p></li></ul><p><strong>Application Details:</strong> </p><p><strong>When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference. </strong></p><p><strong>Applications Accepted: August 24th, 2026 - September 11th, 2026</strong> <br>For more information on the tracks, program, and interview process, please refer to the brochure. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 24 Aug 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager GCP Quality]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50181]]></requisitionid>
    <referencenumber><![CDATA[R50181]]></referencenumber>
    <apijobid><![CDATA[r50181]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50181/senior-manager-gcp-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Quality Management - Global Development to join our Global Development Quality team, supporting our global clinical development organisation in a hybrid work model. In this role, you will lead risk-based quality management across clinical trials while collaborating with study teams, clinical functions, contract research organisations, and quality colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Multiple locations are being considered for this role (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead risk-based quality management across assigned clinical trials</p></li><li><p>Drive protocol-stage Quality Risk Assessment and Control Tracker activities under ICH E6 R3</p></li><li><p>Manage quality issues, audit responses, corrective actions, preventive actions, and trend analysis</p></li><li><p>Partner with study leads, monitoring teams, and contract research organisations on site risks</p></li><li><p>Escalate significant quality events and trends to Executive Quality Leadership</p></li><li><p>Support inspection readiness, responses, and follow-up actions across relevant functions</p></li><li><p>Manage onboarding, development goals, coaching, performance discussions, and team administration</p></li><li><p>You champion quality, integrity, continuous learning, and trusted partnerships</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and eight years’ relevant healthcare or pharmaceutical industry experience</p></li><li><p>Quality, compliance, clinical development, Good Clinical Practice, or Good Pharmacovigilance Practice experience</p></li><li><p>Advanced risk-based quality management, risk assessment, and compliance knowledge</p></li><li><p>Experience managing complex issues, regulatory inspections, and inspection readiness</p></li><li><p>Subject matter expert, process owner, training, presentation, and staff management experience</p></li><li><p>Process improvement, project management, prioritisation, and time management skills</p></li><li><p>Advanced Microsoft Outlook, Word, Excel, and PowerPoint skills</p></li><li><p>Strong communication, collaboration</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[External Manufacturing Specialist, Advanced Therapies]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50173]]></requisitionid>
    <referencenumber><![CDATA[R50173]]></referencenumber>
    <apijobid><![CDATA[r50173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r50173/external-manufacturing-specialist-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill an External Manufacturing Specialist position within the Advanced Therapies team that specializes in synthetic or fermentation-based processes. This role coordinates aspects of contract manufacturing organizations and partners including day-to-day operations, ensuring timely completion of associated operations/documentation, and assisting in the monitoring of cGMP compliance.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York</p></li><li><p>Work schedule: Monday-Friday, 8am-4:30pm</p></li><li><p>Travel: 25%</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Serving as the operational contact for contract manufacturing and/or partner sites concerning day-to-day activities</p></li><li><p>Coordination of external manufacturing activities at contract and/or business partner sites, including but not limited to scheduling of all batches, supply of materials, providing direction on shipment of material, tracking and monitoring of cycle times, providing and enlisting support from others who will provide any required associated reports and technical expertise</p></li><li><p>Functioning as a liaison between Regeneron Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners</p></li><li><p>Supporting investigations and associated shipping operations</p></li><li><p>Supporting and advising critical initiatives and contracts that drive long-term relationship stability and success</p></li><li><p>Ensuring product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers and business partners.</p></li><li><p>Support tech transfer and/or development work of programs at a CMO to ensure scalability toward GMP manufacturing</p></li><li><p>Performing reviews of pre-production master batch records and executed batch records</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in scientific field and the following amount of related experience in cGMP manufacturing operations (clinical and/or commercial), or equivalent combination of education and experience, for each level:</p><ul><li><p>Associate Specialist – 0-2 years</p></li><li><p>Specialist – 2+ years</p></li><li><p>Level will be determined based on experience</p></li></ul></li><li><p>You have experience in any of the following areas: synthetic-based processes, small molecule synthesis, antibody drug conjugates, fermentation</p></li><li><p>You have knowledge of bulk manufacturing techniques (recommended) – fermentation, chemical synthesis, downstream purification, conjugation and/or formulation</p></li><li><p>You have basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines, and EU regulations</p></li><li><p>You have strong interpersonal, written, and oral communication skills</p></li><li><p>You can gain understanding from the instructions provided and work towards goals with minimal supervision</p></li><li><p>Shows resiliency and flexibility in the face of a dynamic environment</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 25 Aug 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
</source>