<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<source>
  <publisher>Regeneron Pharmaceuticals Inc.</publisher>
  <publisherUrl>https://www.regeneron.com/</publisherUrl>
  <lastBuildDate>Fri, 03 Apr 2026 16:35:06 GMT</lastBuildDate>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41999]]></requisitionid>
    <referencenumber><![CDATA[R41999]]></referencenumber>
    <apijobid><![CDATA[r41999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>As an HVAC Technician, a typical day might include the following:</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></ul><p>This role might be for you if you:</p><ul><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>To be considered for the HVAC Technician you ideally should have an 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>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 (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Global Procurement HR & Professional Services]]></title>
    <date><![CDATA[Tue, 16 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44069]]></requisitionid>
    <referencenumber><![CDATA[R44069]]></referencenumber>
    <apijobid><![CDATA[r44069]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44069/executive-director-global-procurement-hr-professional-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[<p>The Executive Director, Global Procurement – HR & Professional Services, is responsible for shaping and executing a forward-thinking global Procurement strategy that aligns with the organization's overarching business objectives and delivers measurable strategic value. This critical leadership role spans HR, Legal, Consulting, Finance & Professional Services, focusing on optimizing procurement performance across these categories to drive competitive advantage and enterprise-wide efficiency.</p><p>Reporting to the Head of Indirect Procurement, the Executive Director will act as the primary representative of Global Procurement in decisions that shape the organization’s HR & Professional Services procurement landscape, influencing both short- and long-term success. The role requires a visionary leader who can anticipate market trends, foster innovation, and build strategic partnerships to deliver lasting value. In addition to driving strategy, the Executive Director will lead and inspire a team of procurement professionals, cultivating a high-performance culture that emphasizes collaboration, innovation, and inclusivity. By providing mentorship and thought leadership, the individual will empower the team to exceed expectations and contribute to the organization’s strategic growth and operational excellence.</p><p><strong>A typical day in this role might look like: </strong></p><ul><li>Collaborate with senior executive leadership within HR & Professional Services and across the organization to identify transformative opportunities and drive innovation, aligning initiatives with strategic objectives to deliver measurable value and competitive advantage</li><li>Lead the development and execution of global HR & Professional Services procurement category strategies, aligning with business and stakeholder priorities.</li><li>Translate category strategies into actionable sourcing projects that deliver measurable value.</li><li>Partner with Indirect Procurement leadership and other stakeholders to ensure strategies evolve with organizational needs and goals.</li><li>Provide expert insight on HR & Professional Services procurement categories, including HR, Legal, Consulting, Finance & Professional Service</li><li>Cultivate and sustain strategic, high-impact relationships with senior executive stakeholders and key suppliers to drive measurable results, influence critical decision-making on make-or-buy operating models, and align procurement initiatives with organizational objectives</li><li>Lead high-impact negotiations and supplier management initiatives. Foster and develop strategic partnerships with key suppliers to drive innovation, value creation, and long-term success.</li><li>Execute a best-in-class vendor management program for HR & Professional Services suppliers and ensure compliance with GxP and applicable regulations.</li><li>Drive process improvements to enhance stakeholder experience and ensure seamless HR & Professional Services service delivery.</li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Bachelor’s degree in a relevant field of study; advanced degree preferred.</li><li>15–20 years of progressive experience in procurement, including substantial experience in HR & Professional Services procurement categories.</li><li>Proven success in leading global categories, teams, processes, and suppliers in a multi-national organization.</li><li>Experience managing senior level professionals and leading cross-functional teams</li><li>Strong negotiation and contract management skills specific to HR & Professional Services vendors and suppliers.</li><li>Proficiency in sourcing and contracting tools, ERP systems, and eRFx platforms (e.g., Oracle, Zycus, Ariba).</li><li>Ability to leverage standard business applications for communication, presentation, and data analysis (Word, Excel, PowerPoint).</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Compliance - コンプライアンスマネージャー]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44121]]></requisitionid>
    <referencenumber><![CDATA[R44121]]></referencenumber>
    <apijobid><![CDATA[r44121]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44121/manager-compliance-%E3%82%B3%E3%83%B3%E3%83%97%E3%83%A9%E3%82%A4%E3%82%A2%E3%83%B3%E3%82%B9%E3%83%9E%E3%83%8D%E3%83%BC%E3%82%B8%E3%83%A3%E3%83%BC/]]></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>Manager, Corporate Compliance – Japan </strong></p><p>We are seeking an experienced Manager, Corporate Compliance to join our dynamic team in Japan. Reporting to the Japan Compliance Lead, you will play a pivotal role in supporting Regeneron’s compliance operations, ensuring the highest standards of ethical conduct and regulatory adherence. This is an exciting opportunity to contribute to the development and implementation of compliance programs that support our mission of advancing science and delivering life-changing medicines. If you are passionate about compliance and working in a collaborative, innovative environment, we invite you to explore this opportunity. </p><p>---</p><p><strong>A Typical Day: </strong></p><p>As the Manager, Corporate Compliance, you will: </p><p>- Collaborate with the Japan Compliance Lead and Global Compliance teams on healthcare compliance (HCC) matters. </p><p>- Implement and operationalize Regeneron’s compliance program and policies in Japan in alignment with headquarters. </p><p>- Develop and refine compliance policies, work instructions, and guidance to ensure adherence to local and international regulations, including JPMA and FTC codes. </p><p>- Deliver engaging compliance training programs for employees and third parties to promote understanding of applicable laws and industry codes. </p><p>- Provide compliance oversight and guidance to ensure interactions with healthcare professionals (HCPs) and organizations (HCOs) are conducted ethically and in accordance with established policies. </p><p>- Conduct internal reviews, risk assessments, and monitoring activities to identify and mitigate compliance risks effectively. </p><p>- Partner with cross-functional teams to provide creative solutions to compliance challenges. </p><p>- Support additional compliance projects and strategies as needed to enhance operations in Japan and the broader APAC region. </p><p>---</p><p><strong>This Role May Be For You If: </strong></p><p>- You have a strong knowledge of the pharmaceutical industry and its self-regulatory framework in Japan, including the JPMA and FTC codes. </p><p>- You thrive in collaborative environments and excel at building cross-functional relationships to achieve compliance goals. </p><p>- You are a problem solver with a creative approach to addressing compliance challenges and implementing practical solutions. </p><p>- You are proactive in identifying risks and opportunities to enhance compliance programs. </p><p>- You have exceptional communication skills in both Japanese and English, with the ability to deliver clear, concise, and impactful messages. </p><p>- You are detail-oriented and committed to maintaining the highest ethical standards in all aspects of your work. </p><p>- You are adaptable and willing to travel to meet the needs of the role. </p><p>---</p><p><strong>To Be Considered: </strong></p><p>We are looking for candidates with a minimum of a BA/BS degree (advanced degrees such as MBA or JD are preferred but not required) and at least 5 years of experience in healthcare compliance-related activities within the pharmaceutical industry in Japan. A strong working knowledge of Japan’s healthcare compliance laws, including the JPMA and FTC codes, is essential. Proficiency in both English and Japanese (written and verbal) is required, along with the ability to draft professional documents and guidance materials. </p><p>If you are ready to take the next step in your compliance career and contribute to a culture of integrity and innovation, we encourage you to apply today. </p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - North Thames]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44778]]></requisitionid>
    <referencenumber><![CDATA[R44778]]></referencenumber>
    <apijobid><![CDATA[r44778]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44778/sales-specialist-north-thames/]]></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 North Thames 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>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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Syracuse, NY]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44944]]></requisitionid>
    <referencenumber><![CDATA[R44944]]></referencenumber>
    <apijobid><![CDATA[r44944]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44944/medical-specialist-i-dermatology-syracuse-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Syracuse]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Syracuse, NY</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p><strong>Geography: Syracuse, Watertown, Binghampton, Ithaca, Elmira</strong></p><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Boston South, Massachusetts]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45062]]></requisitionid>
    <referencenumber><![CDATA[R45062]]></referencenumber>
    <apijobid><![CDATA[r45062]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45062/medical-specialist-i-dermatology-boston-south-massachusetts/]]></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>Geography: Boston South, Massachusetts</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I- Dermatology- Fairfax, VA]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44983]]></requisitionid>
    <referencenumber><![CDATA[R44983]]></referencenumber>
    <apijobid><![CDATA[r44983]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44983/medical-specialist-i-dermatology-fairfax-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Alexandria]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Fairfax, VA</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Atlanta Metro, GA]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45003]]></requisitionid>
    <referencenumber><![CDATA[R45003]]></referencenumber>
    <apijobid><![CDATA[r45003]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45003/medical-specialist-i-dermatology-atlanta-metro-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[<p><strong>Geography: Atlanta Metro, GA</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory. #derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product Specialist Dermatology (Veneto Est - Friuli VG)]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45287]]></requisitionid>
    <referencenumber><![CDATA[R45287]]></referencenumber>
    <apijobid><![CDATA[r45287]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45287/product-specialist-dermatology-veneto-est-friuli-vg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea meets the right team, meaningful change can happen. By working within our growing network to invent, develop, and bring to patients therapies that can transform the lives of people with serious diseases, we are creating new ways of thinking about science, manufacturing, commercialisation - and health.</p><p>Join our new Immunology Sales team in Italy. As a Sales Specialist, you will contribute to achieving Immunology sales targets, always keeping Regeneron’s commitment to patient care at the centre. We are looking for people with a hands-on approach, strong commercial judgement, the ability to manage priorities and resources, and a proven track record of results (meeting or exceeding targets). The ideal candidate thinks critically, organises time effectively, and manages stakeholder engagement in a focused way, bringing value and targeted solutions.</p><p><strong>Job duties</strong></p><ul><li><p>Deliver key brand messages in the territory, aligned with the agreed strategy.</p></li><li><p>Contribute to the development of the territory tactical plan by providing market and local territory insights, in line with the product brand plan.</p></li><li><p>Use available market data to define the action plan for your territory.</p></li><li><p>Manage required administrative activities (expense notes, marketing/field insight reports, call reporting).</p></li><li><p>Operate in compliance with Regeneron regulatory, legal, and compliance guidelines.</p></li><li><p>Participate in local, regional, and national meetings as required.</p></li><li><p>Work collaboratively with alliance partners, contributing to shared objectives.</p></li></ul><p><strong>Requirements</strong></p><ul><li><p>Excellent relationship-building and customer engagement skills, with a value-based focus.</p></li><li><p>Strong scientific and technical knowledge, with the ability to deliver disease and concept selling activities.</p></li><li><p>Strong written, verbal, and presentation communication skills.</p></li><li><p>Strong planning and organisational skills.</p></li><li><p>Ability to present ideas clearly to individuals or groups, adapting the message to the audience.</p></li><li><p>Ability to work independently and contribute to the development of territory tactical plans.</p></li><li><p>Good working knowledge of Microsoft Office (Word, Excel, PowerPoint) and email/CRM tools.</p></li><li><p>Degree (or equivalent qualification) and 5 years’ experience as a pharmaceutical representative (or equivalent role), with hospital-level activity.</p></li><li><p>Experience in the biologics market is a plus.</p></li><li><p>Experience in Dermatology and/or experience working with or engaging hospital paediatricians 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 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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 02:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Oncology]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45258]]></requisitionid>
    <referencenumber><![CDATA[R45258]]></referencenumber>
    <apijobid><![CDATA[r45258]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45258/associate-director-clinical-scientist-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>We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><div><div><div><div><div><div><div><div><p><strong>As an Associate Director a typical day may include the following:</strong></p><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead 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; Member of the Clinical Study Team and Global Clinical SubTeam</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 as well as maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Possesses 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</p></li><li><p>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>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</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><p><strong>This role may be for you if:</strong></p><ul><li><p>Ability to lead activities within a matrix environment; 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><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements.</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree, Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) is preferred. ≥ 10 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking proven leadership experience and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Strong cross-functional management, interpersonal and problem-solving skills. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p></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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director, Clinical Development CV/Renal/Metabolism]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44955]]></requisitionid>
    <referencenumber><![CDATA[R44955]]></referencenumber>
    <apijobid><![CDATA[r44955]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44955/executive-medical-director-clinical-development-cvrenalmetabolism/]]></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>The Executive Medical Director, Clinical Sciences, Obesity is responsible for effectively managing obesity opportunities in an end-to-end framework (clinic entry through lifecycle management). This will require engagement with both Discovery and Medical Affairs as key stakeholders, in addition to other functional stakeholders (e.g., Clinical Pharmacology, Biostatistics, Precision Medicine, Imaging, Genetics Center, Preclinical Safety, Regulatory, Commercial, etc). It requires a rich scientific focus with contribution to obesity strategy: target selection, clinical planning, target engagement, dose selection, proof-of-concept, and pivotal study design and conduct, label negotiation, and lifecycle management. For designated programs, the Clinical Program Lead (CPL) will be responsible for multiple indications driving broader cross functional perspective in the creation of clinical program development strategies. This role reports into the Internal Medicine CVRM VP Therapeutic Area Lead and is also leader of select Global Clinical Sub-Teams for the design, implementation, execution and submission/approval of clinical development programs to support decision milestones and regulatory requirements. </div><div><div><div><div><p>A typical day in the life of an Executive Medical Director may include the following:</p><ul><li>Leads the Global Clinical Subteam (GCST) and clinical development representative at the Strategic Program Team (SPT) for assigned assets, managing all clinical aspects and driving execution of assigned clinical program(s)</li><li>Leads the development and execution of the Clinical Development Plan (CDP) including Phase 1 – 3 trials designed for successful global registration of the compound.</li><li>Leads creation of clinical components of key documents (regulatory documents, registration dossiers, etc.) supporting registration, market access, and commercialization of the compound(s).</li><li>Acts as medical expert and leader in interactions with external and internal stakeholders</li><li>Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety.</li><li>Ensures quality of all clinical documents (e.g., Investigators’ Brochure, protocol, study report, clinical components of regulatory submissions, safety related documents) produced by GCST</li><li>Builds and leads effective teams. Manages and oversees activities of teams up to Senior Medical Director level; Establishes operational objectives and work plans, delegating assignments to subordinate staff.</li><li>Partner with operations team to ensure high quality execution of the clinical development portfolio</li><li>Partners and helps lead BD processes.</li></ul><p>This job may be for you if you have the following:</p><ul><li>MD or MD/PhD required with specialized residency and fellowship training; >8 years of involvement in clinical research or drug development in an industry environment spanning clinical activities in Phases 1 through 4. </li><li>≥6 years people management experience desirable, this may include management in a matrix environment. </li><li>Strong management, interpersonal, communication, negotiation and problem-solving skills. </li><li>Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally. </li><li>Medical/scientific expertise in Endocrinology, CV/Metabolism, and/or Obesity is strongly preferred</li><li>Understanding of global regulatory environment including key regulatory agencies and approval processes</li><li>Strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out)</li></ul><p>This role requires 4 days per week on-site in Tarrytown, NY</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p></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>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Automation Engineer (Process)]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45448]]></requisitionid>
    <referencenumber><![CDATA[R45448]]></referencenumber>
    <apijobid><![CDATA[r45448]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45448/principal-automation-engineer-process/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Principal Automation Engineer to support manufacturing operations at the Raheen site. This Role will require extensive experience in design, implementation and optimization of automated industrial and manufacturing processes.</p><p><strong>As a Principal Process Engineer, a typical day might include the following:</strong></p><ul><li>Programming, diagnosing, and troubleshooting Emerson DeltaV (ISA‑88 batch), Allen‑Bradley/Rockwell PLCs, and HMI applications for bioreactors, chromatography skids, clean utilities (WFI/clean steam)</li><li>Owning full automation project lifecycle: URS, design, FAT/SAT, IQ/OQ/PQ, CSV, and turnover—ensuring robust schedules and coordination with Manufacturing, QA, Validation, and Facilities</li><li>Implementing software changes under formal cGMP change control with impact assessments; update SOPs and training materials</li><li>Authoring engineering documents, risk assessments (e.g., FMEA), and test plans per GAMP 5; enforce 21 CFR Part 11 and ALCOA+ data integrity (audit trails, electronic signatures, role‑based access)</li><li>Providing site support, troubleshooting operations, participating in deviations/CAPA and investigations, and delivering 24/7 on‑call coverage</li><li>Maintaining and diagnosing instrumentation and automation hardware; managing legacy item and coordinating lifecycle upgrades</li><li>Configuring and supporting controls networks and protocols (EtherNet/IP, Modbus, Profibus); integrating with historians, MES (ISA‑95) where applicable.</li><li>Driving continuous improvement via recipe optimization, alarm rationalization, OEE/performance monitoring, and reduction of batch cycle time</li><li>Managing automation contractors and supporting commissioning, tech transfer, and documentation traceability</li><li>Approving hardware, software, and control strategies emphasizing compliance, reliability, and patient safety</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have a demonstrated capability for leading complex projects technically from initial design / development through to the validation of the facility in support of defined objectives</li><li>Have direct experience and in depth knowledge of Allen Bradley Rockwell/Emerson Delta V automation platform</li><li>Have demonstrated leadership with the ability to work on own initiative without direct supervision from management and provide mentoring to other members of the automation group when required</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better</li></ul><p>To be considered for this position you should have a Bachelor's degree in Science, Chemical, Mechanical, or Electrical Engineering and 8+ years experience working with validated Automation systems in a pharmaceutical manufacturing environment. </p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 03:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Consumer Marketing - Respiratory]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45324]]></requisitionid>
    <referencenumber><![CDATA[R45324]]></referencenumber>
    <apijobid><![CDATA[r45324]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45324/associate-director-consumer-marketing-respiratory/]]></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>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, atopic dermatitis, asthma, COPD, chronic rhinosinusitis with nasal polyps (CRSwNP), eosinophilic esophagitis (EoE), oncology, hypercholesterolemia, and rare inflammatory conditions. Regeneron also has product candidates in development in other areas of high unmet medical need.</p><p>The Associate Director of Pulmonology Consumer Marketing is responsible for the development and implementation of U.S. consumer marketing strategies for all current and future respiratory indications and for collaborating with cross-functional partners to ensure strategic alignment and execution. This role reports to the Senior Director, Pulmonology Consumer Marketing Lead.</p><p><strong>In this role, a typical day may include the following:</strong></p><ul><li>Develop the Consumer Pulmonology marketing strategy and ensure alignment with the overall brand strategy across all current and future Pulmonology indications.</li><li>Collaborate effectively in a matrixed working environment and within a strategic alliance.</li><li>Oversee media planning and buying across digital and offline channels, including TV/online video, programmatic and endemic display, social, and search.</li><li>Effectively convey and advocate for the Consumer Pulmonology marketing strategy among key internal team members and throughout the alliance.</li><li>Build and maintain a CRM platform across online and offline channels, and oversee the creation of email and other communications.</li><li>Manage multiple agencies to build creative across the digital ecosystem (e.g., website, banners, social ads, emails).</li><li>Foster strong partnerships with Sales, Medical Affairs, Corporate Communications, Market Research, Patient Support Services, Legal, and other cross-functional partners to ensure aligned objectives at Regeneron and across the alliance.</li><li>Ensure that marketing processes and programs align with corporate guidance and regulatory, legal, and ethical guidelines.</li><li>Monitor spend against budget and manage projects to agreed-upon timelines, budgets, and scope.</li></ul><h3><strong>This role may be for you if you:</strong></h3><ul><li>Are well-versed in DTC media and return-on-investment analysis across all DTC channels.</li><li>Apply expertise in digital media execution and CRM, including working with creative agencies and navigating regulatory/legal review processes (e.g., MLR, JRC).</li><li>Bring strong project management and organizational skills with the ability to manage multiple priorities in a fast-paced environment.</li><li>Demonstrate strategic, scientific, and analytical competence and are focused on delivering results.</li><li>Have strong communication and presentation skills, capable of articulating complex strategies to partners at all levels, including senior leaders, regardless of their technical background.</li></ul><h3><strong>To be considered for this role, you have:</strong></h3><p>A bachelor’s degree (required); an MBA is a plus. You bring 10+ years of progressive industry or relevant professional experience in strategic roles with a focus on consumer omnichannel strategy and franchise management. Experience navigating and managing complex alliance partnerships is preferred. Respiratory/immunology experience is preferred. Lastly, you are willing to work in a hybrid environment with a minimum of four days on-site in Sleepy Hollow, NY.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 06:56:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager,  Medical Affairs Finance]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45668]]></requisitionid>
    <referencenumber><![CDATA[R45668]]></referencenumber>
    <apijobid><![CDATA[r45668]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45668/manager-medical-affairs-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>We are seeking a Manager to join our finance team in support of Regeneron’s Medical Affairs organization. This role will be essential in partnering with the Finance Lead to manage both current and long-term financial goals, maintaining budget discipline across multiple commercialized products as well as an expanding pipeline of clinical assets. </p><div><p>Key responsibilities include preparing annual budgets and quarterly forecasts, acting as a controller by analyzing variances between actual results and budgets, creating monthly reporting packages, and supporting the Finance Lead with various ad-hoc reports and analyses for all commercial and clinical-stage products. The manager will also collaborate with different functions and therapeutic leads within Medical Affairs to provide insights, gather data, and enhance existing financial processes. </p></div><div><p>If you are passionate about finance and innovative medicine, and want to contribute to a company known for delivering important medicines to patients, this is an opportunity worth considering. </p></div><div><p><strong>A Typical Day in the Role Might Look Like:</strong> </p></div><div><ul><li><p>Collaborate with teams to stay updated on decisions and their financial effects, requiring an understanding of Medical Affairs’ roles in development and commercialization. </p></li></ul></div><div><ul><li><p>Lead quarterly forecasting and yearly planning sessions. Prepare and present analyses and reports, including for Phase IV clinical trials when needed. </p></li></ul></div><div><ul><li><p>Conduct research and analysis to provide insights that inform business decisions. </p></li></ul></div><div><ul><li><p>Update financial models monthly to support timely decision-making, which includes accruals, reclassifications, and other updates. </p></li></ul></div><div><ul><li><p>Assist the Finance Lead as needed with ad-hoc financial analyses. </p></li></ul></div><div><ul><li><p>Identify and implement ongoing process improvements within the Medical Affairs Finance Team. </p></li></ul></div><div><p><strong>This Role Might Be for You If You Are: </strong> </p></div><div><ul><li><p>Proactive and analytical with creative problem-solving skills and a focus on process improvement. </p></li></ul></div><div><ul><li><p>Able to make sound judgments and conclusions even with limited information. </p></li></ul></div><div><ul><li><p>Demonstrate quantitative, analytical, and problem-solving abilities. </p></li></ul></div><div><ul><li><p>Comfortable working in a collaborative, fast-paced, and sometimes ambiguous setting. </p></li></ul></div><div><ul><li><p>Intellectually curious and organized, able to set priorities and follow through independently. </p></li></ul></div><div><ul><li><p>Excellent communication skills. </p></li></ul></div><div><ul><li><p>A positive team player eager to learn. </p></li></ul></div><div><p>This role requires a BS or MS and 6-10 yrs experience. CPA/MBA strongly required. Strong expertise with Microsoft Excel, including Pivot Tables, charts, and formulas. Solid understanding of finance, accounting principles, and P&L statements. Familiarity with clinical trial processes and post-marketing studies. Experience with planning tools like Hyperion Planning is a plus. Knowledge of reporting and dashboard tools (Hyperion, Qlik, Cognos) is advantageous. Proficiency in Microsoft PowerPoint. </p></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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Diagnostics]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45732]]></requisitionid>
    <referencenumber><![CDATA[R45732]]></referencenumber>
    <apijobid><![CDATA[r45732]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45732/associate-director-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>This role provides an exciting opportunity to lead projects across diverse therapeutic areas. As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy, development, and lifecycle management of companion diagnostic solutions that enable our therapeutics. This role drives cross-functional alignment across biomarker science, clinical development, regulatory, commercial, and external IVD partners to deliver fit-for-purpose assays that meet global regulatory requirements and support clinical decision-making. You will lead the CDx portfolio from early biomarker feasibility through clinical validation, registration, launch, and post-market sustainment, ensuring timely availability of high-quality diagnostics aligned with drug development milestones.</p><p><strong>A typical day might include</strong>:</p><ul><li><p>Set the global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines for the therapeutic.</p></li><li><p>Lead selection and oversight of IVD partners; negotiate scopes, timelines, budgets, and quality expectations; manage co-development and governance.</p></li><li><p>Define assay intent and target product profiles (TPP) for CDx platforms (e.g., NGS, PCR, IHC, Immunoassays), ensuring analytical and clinical performance meets intended use.</p></li><li><p>Partner with biomarker and clinical teams to integrate CDx into trial designs (screening, enrichment, stratification), including sample strategy and operational readiness.</p></li><li><p>Drive analytical validation plans (e.g., accuracy, precision, sensitivity/specificity, LoD, reproducibility) and clinical validation strategies linking assay results to drug safety and efficacy.</p></li><li><p>In collaboration with IVD Regulatory, support global regulatory strategy and submissions for CDx (e.g., FDA PMA/supplement, 510(k) where applicable, EU IVDR, PMDA), including pre-submission interactions and labeling alignment.</p></li><li><p>Ensure compliance with applicable standards and regulations (e.g., ISO 13485, ISO 14971, CLSI guidelines, IVDR, GCP alignment for diagnostic use in trials).</p></li><li><p>Coordinate cross-functional working groups, remove program obstacles, and provide transparent status reporting to governance bodies.</p></li><li><p>Oversee design transfer, manufacturing readiness, and supply planning with IVD partners to ensure clinical and commercial availability.</p></li><li><p>Drive risk management and mitigation plans across technical, regulatory, operational, and commercial domains.</p></li><li><p>Partner with commercial and medical affairs to shape CDx launch readiness (access, coverage, distribution, training, KOL engagement).</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>Proven track record delivering CDx aligned to drug approvals, including successful analytical/clinical validation and regulatory submissions.</p></li><li><p>Deep understanding of diagnostic platforms (NGS, PCR, IHC, Immunoassays) and associated validation standards and quality systems.</p></li><li><p>Experience managing external IVD partners and complex, cross-functional programs.</p></li><li><p>Strong knowledge of global regulations (FDA CDRH, EU IVDR, PMDA) and pathways for CDx approval and labeling.</p></li><li><p>Excellent communication, leadership, and stakeholder management skills.</p></li><li><p>Strategic thinking with the ability to translate scientific and clinical needs into executable diagnostic solutions.</p></li><li><p>Program leadership, planning, and risk management across multiple, fast-paced workstreams.</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><ul><li><p>Advanced degree in a relevant field (e.g., MS/PhD in molecular biology, pathology, biomedical engineering, or related) or equivalent experience.</p></li><li><p>8+ years of experience in diagnostics development, with 4+ years leading CDx or IVD programs in pharmaceutical or diagnostics settings</p></li></ul><p><strong>Travel:</strong></p><p>Travel up to 5–10% for partner meetings, clinical site visits, and regulatory interactions.</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, IT Product Management - Financials]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45506]]></requisitionid>
    <referencenumber><![CDATA[R45506]]></referencenumber>
    <apijobid><![CDATA[r45506]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45506/associate-director-it-product-management-financials/]]></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, IT Product Management –Financials you will lead the IT execution, delivery and operational ownership of Regeneron’s Record to Report (RTR) capabilities within a modern global ecosystem. This role is accountable for translating product strategy and roadmap direction into high-quality, scalable, and compliant solutions that support Global Finance, including Record‑to‑Report, Tax, Treasury, and integrated financial workstreams.</p><p>Success in this role requires not only deep Oracle EBS and Fusion RTR expertise, but also deep Financials, Tax and Treasury industry knowledge.</p><div></div><p>A typical day in this role might look like:</p><ul><li>Act as a strategic and trusted partner to Finance stakeholders and help with Business Roadmap and Strategy, and delivering on Business outcomes and value framework</li><li>Serve as the IT Product owner for not only Oracle ERP Financials but also associated boundary systems and processes like, VAT, Sales Tax, Reval Treasury Management systems, AGIS, Concur, Intercompany, Lease Accounting, Project Accounting, Accounting Hub, and Collaboration Billing.</li><li>Drive execution across multiple concurrent workstreams while balancing strategic transformation and day‑to‑day operational needs, focused on supporting Global growth</li><li>Lead a portfolio of ERP Financials initiatives in partnership with the PMO, including demand intake, prioritization, planning, execution, vendor management, and financial oversight.</li><li>Partnering strategically with business for Vendor Selections, RFPs, Total Cost of ownership and Cost benefit analysis, Application rationalization on an ongoing basis.</li><li>Provide oversight of system integrators and vendors, ensuring delivery aligns with enterprise standards, Oracle best practices, and future‑state architecture.</li><li>Lead ongoing improvements, configuration changes, and enhancements including but not limited to Oracle ERP and key boundary systems to improve efficiency and support evolving business needs.</li><li>Ensure application, integration, and data architecture standards are defined, maintained, and aligned across the ERP Financials ecosystem.</li><li>Oversee data migration and conversion activities related to ERP Financials, ensuring accuracy, reconciliation, and audit readiness.</li><li>Drive integrated and automated financial processes across upstream and downstream systems.</li><li>Maintain strong Identity and Access Management controls (RBAC / ABAC) across sensitive financial systems.</li><li>Partner with Infosec and other technology teams to ensure alignment with Regeneron security standards and ensure compliance on ERP platforms, SaaS, and third-party applications for patching, data security, privacy, security, risk, and regulatory standards.</li><li>Promote a data‑driven mindset, leveraging Oracle reporting and analytics tools (OTBI, BI Publisher, FDI, FRS, Smart View).</li><li>Apply emerging technologies, automation, and AI‑enabled capabilities to modernize financial operations and improve insight.</li><li>Ensure ERP Financials capabilities support global reporting, close, decision‑making needs.</li></ul><p>This role might be for you if you have:</p><ul><li>Strong understanding of ERP Financials processes including Record‑to‑Report, Intercompany, and Project Accounting, Tax, Treasury, Forex.</li><li>Strong understanding of enterprise Chart of Accounts (COA) design and governance, including structure, harmonization, mapping rules.</li><li>Strong understanding of SOX, ITGC, and regulated environments</li><li>Strong problem analysis and resolution skills for both functional and end-to-end solution.</li><li>Ownership mindset, resilience, willingness to roll up sleeves to ensure delivery success.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in a related field (Accounting, Finance, Information Systems, Computer Science, or similar) and 10+ years of increasing responsibility delivering Oracle ERP Financials solutions plus a minimum of 4+ years partnering closely with Global Finance across multi‑functional workstreams and Oracle Fusion experience. Knowledge of EPM (ARCS,FCCS, EPBCS, PCMCS), Planning and Consolidation would be a plus.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Finance]]></title>
    <date><![CDATA[Thu, 05 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45804]]></requisitionid>
    <referencenumber><![CDATA[R45804]]></referencenumber>
    <apijobid><![CDATA[r45804]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45804/director-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>About Regeneron</strong> </p></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></div><div></div><div><p>As a Finance Director you will serve as the Finance Partner for India and act as a key interface with global CFO functions. You will lead critical planning and forecasting, drive performance insights, ensure governance, and support strategic decisions that enable our business outside the US to scale.</p></div><div><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p></div><div></div><div><p><strong>A typical day may include the following: </strong> </p></div><div><ul><li><p>Serve as the Finance Partner for India, contributing to leadership discussions and business planning </p></li></ul></div><div><ul><li><p>Provide forward-looking insights that influence decisions on cost, growth, resourcing, and profitability </p></li></ul></div><div><ul><li><p>Act as the local steward for governance and compliance related to CFO policies and controls </p></li></ul></div><div><ul><li><p>Lead country-level budgeting and forecasting, including system submission and management presentations </p></li></ul></div><div><ul><li><p>Drive Actuals vs Forecast variance analysis with actionable recommendations </p></li></ul></div><div><ul><li><p>Implement tools and handle resource planning/FTE utilization across programs and cost centers </p></li></ul></div><div><ul><li><p>Partner with Accounting to review legal entity financial data and financial documents, ensuring accuracy and clarity </p></li></ul></div><div><ul><li><p>Liaise with Treasury to ensure local operations are adequately funded; provide cash forecasts </p></li></ul></div><div><ul><li><p>Coordinate with Tax on annual filings, ensuring accurate inputs for calculations and forecasts </p></li></ul></div><div><ul><li><p>Support broader ex-US consolidation and above-country finance planning and analysis as required </p></li></ul></div><div><p><strong>This job may be for you if you have:</strong> </p></div><div><ul><li><p>Strong expertise in forecasting, budgeting, governance, and business partnering </p></li></ul></div></div><div><div><ul><li><p>A proven ability to operate in ambiguity, influence stakeholders, and drive outcomes proactively </p></li></ul></div><div><ul><li><p>Executive communication skills — able to translate numbers into decisions </p></li></ul></div><div></div><div><p>To be considered for this role you must have 12+ years post-qualification experience in Finance leadership, ideally within the biotech/pharma industry, or Shared Service/Global Capability environment. You will have a relevant undergraduate degree; with MBA/CA/CMA/CPA or equivalent preferred. You will be proficient in English & local language. </p></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Mar 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[EHS Site Lead]]></title>
    <date><![CDATA[Fri, 06 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45444]]></requisitionid>
    <referencenumber><![CDATA[R45444]]></referencenumber>
    <apijobid><![CDATA[r45444]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45444/ehs-site-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As the Site Lead for EHS you will own and drive the strategy for Environmental, Health and Safety compliance and Security operations (EHS). You will direct the implementation and evolution of the IOPS EHS Management Systems to ensure that EHS is central to the overall operations on the Raheen campus.</p><p><strong>In this role a typical day might include the following:</strong></p><ul><li><p>Providing leadership and developing EHS objectives to deliver improvements, foster cooperation and develop a strong EHS culture across all functions and at all levels of the organization</p></li><li><p>Collaborating with Site Management to identify improvements in the EHS System’s overall effectiveness, adequacy and suitability to meet ongoing risks and changes</p></li><li><p>Maintaining metrics to measure performance against EHS objectives and make necessary changes to improve performance</p></li><li><p>Guiding, developing and supporting the EHS Team through coaching and supervision</p></li><li><p>Participating in all Health and Safety audits and inspections and coordinating responses with the appropriate agencies or groups</p></li><li><p>Proactively seeking out opportunities to learn best practices from other organisations and apply these learnings to the Regeneron setting</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Display strong influencing capabilities to bring stakeholders together and drive a site-wide EHS culture</p></li><li><p>Possess excellent communication and interpersonal skills</p></li><li><p>Have demonstrated experience in building successful partnerships with cross-functional teams</p></li><li><p>Can demonstrate a proven track record managing and mentoring people</p></li><li><p>Have the ability to manage multiple projects and priorities in a dynamic, fast-paced setting</p></li></ul><p>To be considered for this position you should have a Health and Safety Diploma/Degree and 10+ years of experience working in an EHS management role in a highly regulated manufacturing facility.</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 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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 05:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Operations Manager, Process & Procedures]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45064]]></requisitionid>
    <referencenumber><![CDATA[R45064]]></referencenumber>
    <apijobid><![CDATA[r45064]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45064/operations-manager-process-procedures/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Are you passionate about streamlining processes and creating impactful procedural documents? Join our Global Development team as an Operations Manager, Process & Procedures, where you’ll drive the development and management of our controlled procedural document portfolio. This role offers the opportunity to contribute to process innovation and collaborate with cross-functional teams in a dynamic, regulated environment. Based in our Tokyo office, this position is your chance to make a meaningful impact while advancing your career.</p><p><strong>A Typical Day:</strong></p><ul><li>Lead the revision and creation of procedural documents through their lifecycle, including updates for process improvements and administrative changes.</li><li>Facilitate process mapping and content updates in collaboration with authors and subject matter experts (SMEs).</li><li>Support procedural document projects by partnering with functional owners and cross-functional SMEs to improve existing processes.</li><li>Coordinate review cycles and approval workflows for assigned procedural documents.</li><li>Identify and evaluate process gaps, proposing effective resolutions to enhance efficiency.</li><li>Partner with Quality Leads and Managers to strengthen procedural document quality and address findings.</li><li>Maintain the Global Development procedural document portfolio for assigned areas.</li><li>Collaborate with training teams to ensure procedural training requirements are implemented effectively.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You thrive in a collaborative environment and enjoy working with cross-functional teams to achieve shared goals.</li><li>You are detail-oriented and excel at identifying gaps in processes and proposing innovative solutions.</li><li>You have strong organizational and project management skills, balancing multiple priorities with ease.</li><li>You possess expertise in controlled procedural document principles and process design.</li><li>You are proficient in tools like Microsoft Visio for process mapping and have experience with electronic document management systems.</li><li>You value integrity and trust, and you’re skilled at negotiating and influencing at all organizational levels.</li><li>You enjoy strategic thinking and problem-solving in a regulated environment.</li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor’s degree and at least 5 years of experience in a global regulated organization, with 3 years in a quality role focusing on procedural documents. Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements, as well as experience in controlled document principles, is essential. Preferred qualifications include expertise in Microsoft Visio or similar tools and familiarity with electronic document management systems. Native level fluency in Japanese and business level English is required.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Cell Therapy)]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43023]]></requisitionid>
    <referencenumber><![CDATA[R43023]]></referencenumber>
    <apijobid><![CDATA[r43023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43023/senior-manager-clinical-study-lead-cell-therapy/]]></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>The <strong>Senior Clinical Study Lead</strong> (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is 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 out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives. </p></div><div><div><div><div><p><em>This role is not eligible fully remote. This role is required to be onsite in one of our locations. (Armonk, NY / Warren, NJ / Cambridge, MA / Dublin, Ireland / Uxbridge, London)</em></p><p><strong>A typical day in this role looks like: </strong> </p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Provides operational input into protocol development</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Ensures compliance with the clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors </p></li><li><p>Provides input into baseline budget development and management</p></li><li><p>Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level</p></li><li><p>Leads the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Oversees/conducts site evaluation and selection</p></li><li><p>Leads investigator meeting preparation and execution</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</p></li><li><p>Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Ensures accurate budget management and scope changes for internal and external studies</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Oversees the execution of the clinical study against planned timelines, deliverables and budget</p></li><li><p>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</p></li><li><p>Ensure clinical project audit and inspection readiness through the study lifecycle</p></li><li><p>Supports internal audit and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>Contributes to clinical study report writing and review</p></li><li><p>Facilitates and contributes to study level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables</p></li><li><p>Recommends and participates in cross-functional and departmental process improvement initiatives</p></li><li><p>Responsible for identification of innovative approaches to clinical study execution including global considerations 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><li><p>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require 25% travel</p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Exceptional interpersonal & leadership skills</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Advanced communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Strong budget management experience</p></li><li><p>An awareness of relevant industry trends</p></li><li><p>Ability to build, lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Advanced project management skills, cross-functional team leadership and organizational skills</p></li><li><p>Line management experience</p></li></ul><p><strong>In order to be considered qualified, </strong>a minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience.</p><p>A background in clinical trials within cell therapy and early phase clinical trials is preferred.</p></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>$148,300.00 - $241,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Oncology]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45863]]></requisitionid>
    <referencenumber><![CDATA[R45863]]></referencenumber>
    <apijobid><![CDATA[r45863]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45863/associate-director-clinical-scientist-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>We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>As an Associate Director a typical day may include the following:</strong></p><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead 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; Member of the Clinical Study Team and Global Clinical SubTeam</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 as well as maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Possesses 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</p></li><li><p>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>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</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><p><strong>This role may be for you if:</strong></p><ul><li><p>Ability to lead activities within a matrix environment; 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><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements.</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree, Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) is preferred. ≥ 10 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking proven leadership experience and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Strong cross-functional management, interpersonal and problem-solving skills. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Corporate Finance]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45950]]></requisitionid>
    <referencenumber><![CDATA[R45950]]></referencenumber>
    <apijobid><![CDATA[r45950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45950/associate-manager-corporate-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>Regeneron Corporate Finance is seeking an Associate Manager to join the team and support enterprise-level financial planning, forecasting, and reporting. This role operates at the center of FP&A and requires strong financial judgment, ownership of complex analyses, and the ability to partner effectively across Finance and with senior stakeholders.</p><p><br> </p><p>The Associate Manager will independently own key corporate finance deliverables and models, support cross-functional partners, and contribute to leadership and Board-level materials. This position is well-suited for a high-performing individual contributor who is comfortable operating with limited direction while exercising sound financial judgment.</p><div></div><p><strong>A Typical Day in This Role Might Look Like</strong></p><ul><li><p>Execute key corporate finance deliverables, including Board presentations, the annual budget, monthly finance package, quarterly earnings support materials, and quarterly financial guidance packages</p></li><li><p>Serve as an owner of core corporate financial models, ensuring accuracy, consistency, and appropriate controls across budgeting, forecasting, and reporting cycles</p></li><li><p>Lead forecasting of key corporate inputs, including people expense, stock-based compensation, royalty income, amortization related to transactions, fully diluted share count, and free cash flow</p></li><li><p>Partner with functional finance teams to review forecast-to-forecast and actual-to-forecast variances, identify key drivers, and communicate implications to leadership</p></li><li><p>Work closely with Accounting to incorporate quarterly actuals, align on Non-GAAP adjustments, and ensure appropriate accounting treatment of transactions and collaborations is reflected in corporate forecasts</p></li><li><p>Collaborate with Tax to prepare quarterly legal-entity financials used in forecasting the effective tax rate</p></li><li><p>Partner with Treasury to prepare cash flow statements and forecast equity-related activity, including stock options, restricted stock, and share repurchases</p></li><li><p>Prepare ad hoc financial analyses and executive-ready presentation materials for the Leadership Team and Board of Directors</p></li><li><p>Identify and implement opportunities to improve forecasting processes, models, and standard deliverables, contributing to efficiency, consistency, and clarity across Corporate Finance</p></li><li></li></ul><div></div><p><strong>This Role May Be for You If You</strong></p><ul><li><p>Demonstrate strong decision quality and are comfortable making, explaining, and defending assumptions in situations involving ambiguity</p></li><li><p>Can independently own complex analyses and operate effectively with limited direction</p></li><li><p>Are comfortable interacting with and presenting to senior management</p></li><li><p>Balance speed and precision while managing competing priorities and tight deadlines</p></li><li><p>Communicate complex financial information clearly and concisely, both in writing and in presentations</p></li><li><p>Produce accurate, well-structured, executive‑-ready‑ analyses and presentation materials</p></li><li><p>Act as a finance advisor to cross-functional stakeholders, providing clear analysis and recommendations</p></li><li></li></ul><div></div><p><strong>Qualifications</strong></p><ul><li><p>BS in Finance, Accounting, Economics, or a related field; MBA, CPA, or CFA preferred</p></li><li><p>Typically, 5–7+ years of progressive, relevant experience in corporate finance, FP&A, investment banking, equity research, or a related analytical role</p></li><li><p>Advanced Excel‑based financial modeling capabilities required</p></li><li><p>Demonstrated experience owning integrated financial models supporting budgeting, forecasting, and strategic analysis</p></li><li><p>Strong analytical, critical thinking and problem-solving skills</p></li><li><p>Experience with financial systems; Hyperion experience strongly preferred</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>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Allentown-PA]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45973]]></requisitionid>
    <referencenumber><![CDATA[R45973]]></referencenumber>
    <apijobid><![CDATA[r45973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45973/medical-specialist-i-dermatology-allentown-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Allentown]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Allentown, PA</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Biostatistician - Genetic Medicine]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46056]]></requisitionid>
    <referencenumber><![CDATA[R46056]]></referencenumber>
    <apijobid><![CDATA[r46056]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46056/principal-biostatistician-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 within Global Development.</p><p><strong>A typical day might include:</strong></p><p>The incumbent will work 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 co-author clinical study protocols, statistical analysis plans, and perform statistical analyses for interim and final reports. The incumbent will also develop and deliver training to non-statistical colleagues, collaborate on development of new infrastructure and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and publications.</p><p><strong>This role might be for you if you can:</strong></p><ul><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>Develop individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.</p></li><li><p>Collaborate with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting. </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>Analyze data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making. </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 or related disciplines with internship experience, or MS degree in statistics/biostatistics with >5 years’ experience in the pharmaceutical industry as a statistician. </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 such as R or SAS is required</p></li></ul><p>#GDBDMJobs</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 16:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II-Ophthalmology-Indianapolis]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41794]]></requisitionid>
    <referencenumber><![CDATA[R41794]]></referencenumber>
    <apijobid><![CDATA[r41794]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41794/medical-specialist-ii-ophthalmology-indianapolis/]]></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>Geography: Indianapolis</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><strong>A typical day might include the following: </strong></p><p>The Ophthalmology 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>This role may be for you if you have:</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>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. Buy and Bill experience. Ophthalmology with relevant retina experience is preferred. Must be based in or located in close proximity to the assigned territory (relocation will not be provided). Ability to travel (40-60%).</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>$152,300.00 - $195,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 11:56:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Pharmacometrics Programmer]]></title>
    <date><![CDATA[Sun, 29 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46221]]></requisitionid>
    <referencenumber><![CDATA[R46221]]></referencenumber>
    <apijobid><![CDATA[r46221]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46221/principal-pharmacometrics-programmer/]]></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>A Principal Pharmacometrics Programmer provides timely support to the study team on all programming matters according to the project strategies.</p><p>Create initial TFLs list for CP report based study SAP and CP TFL standards; Finalized the list with the input from author and writer. Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement, Population PK/Population PK/PD analysis requirement and programming specifications using internal standards and guidelines. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment, 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. Lead/participate projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Address statistical ad-hoc requests of senior management, HA, performing exploratory ER analysis upon the requests.</p><p><strong>This position requires 4 days onsite presence based out of our Tarrytown, NY or Warren, NJ location.</strong></p><p><strong>In this role, a typical day might include the following: </strong></p><p>· lead programmer for programming and QC of analysis datasets, TFL's of 1 or more projects following Regeneron standard data models or user requirements. Representation of PMX programming functions and coordination of activities with cross line functions and communicate shifting timelines and milestones. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. Contribute to standard tools or macros development.</p><p>· Integration of data across studies in support of Exposure-response, PopPK and PopPKPD analysis and 2.7.2. Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</p><p>· Lead and execute the creation and validation of electronic data submission packages according to CDISC standards (i.e. annotated CRF, data export files, CSDRG, ADRG, define documents).</p><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 report</p><p>· Participate in department working groups; participate/provide input in development of tools and improvement of processes.</p><p>Adheres to the SOPs, Guidelines, Working Instructions when processing/analyzing/storing/transferring the data.</p><p><strong>This role may be for you if have:</strong></p><p>· Strong SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment</p><p>· Good understanding of relational database structure.</p><p>· Understanding of reporting systems utilizing multiple data delivery applications; Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards.</p><p>· Able to take directives, works independently, exercises 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><p>· Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis), experienced in data handling, process and analysis and able to undstand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner</p><p>· Experience in project management with supervision. Ability to organize and manage multiple assignments with challenging timelines for a limited number of personnel.</p><p>Skilled in use of relevant software, including Window SAS, SAS EG (Base, Stat, Macro, graph), MS-Excel, R,/R-Studio etc.</p><p><strong>To be considered for this opportunity you must have:</strong></p><p>MS. (BS.) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 30 Mar 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Project Management (Strategic Alignment)]]></title>
    <date><![CDATA[Sun, 29 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46128]]></requisitionid>
    <referencenumber><![CDATA[R46128]]></referencenumber>
    <apijobid><![CDATA[r46128]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46128/director-project-management-strategic-alignment/]]></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>Regeneron is looking for a Director Project Management (Strategic Alignment) at our IOPS (Industrial Operations Product Supply) location to lead the enterprise “operating system” for strategy. In this role you will drive clarity, alignment, and cohesive execution by translating priorities into actionable objectives and reinforcing them through planning, communication, and performance management.</p><p><strong>A typical day in this position may include:</strong></p><ul><li>Align senior leadership on long‑term priorities and enterprise objectives.</li><li>Run annual and quarterly strategic planning and alignment processes.</li><li>Maintain strategy artifacts: 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.</li><li>Define enterprise KPIs and indicators; integrate resourcing and capacity into prioritization.</li><li>Maintain scorecards; synthesize performance trends and variance analysis into leadership insights.</li><li>Coordinate executive reviews and ensure evidence‑based decisions and follow‑through.</li><li>Scan external trends; translate signals into strategic implications and actions.</li><li>Identify capability gaps; partner with L&LD, Tech Training, HRBPs to build skills aligned to strategy.</li><li>Craft clear strategy narratives and communication materials; sustain organization‑wide understanding.</li></ul><p><strong>This role may be for you if you have experience with:</strong></p><ul><li>Enterprise operating model design; planning and review rhythms; cross‑functional alignment.</li><li>Executive communication, facilitation and can influence across diverse leaders.</li><li>Organizational capability building; change in mindset, skillset, and behaviors.</li><li>Data fluency with KPIs, dashboards, scorecards; insight‑to‑action translation.</li></ul><ul><li>Knowledge Management: frameworks, repositories, standards, playbooks, and insight archives.</li><li>Employee Engagement Insights: sentiment analysis integrated into strategic alignment and change readiness.</li><li>Creative Services: executive presentations, visual narratives, and alignment tools.</li></ul><p>To be considered for this role you must have Bachelor’s degree in Business Administration, Engineering, Organizational Leadership, or a related field, and 12+ years of relevant project management experience. A master’s degree in business administration (MBA) or Organizational Leadership is preferred.</p><p>Level is determined based on qualifications relevant to the role.</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>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 30 Mar 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Trade & Distribution]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46153]]></requisitionid>
    <referencenumber><![CDATA[R46153]]></referencenumber>
    <apijobid><![CDATA[r46153]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46153/senior-manager-trade-distribution/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Trade & Distribution Operations is a key member of the team, responsible for end‑to‑end oversight of distribution and order fulfillment across Spain/France, Switzerland, and EU Rare Disease channels. Collaborating with internal teams, external vendors, customers, and logistics partners, you will be driving operational performance, vendor collaboration, regulatory/GDP compliance, budget stewardship, and continuous improvement to ensure reliable, efficient delivery.</p><p><strong>A Typical Day</strong></p><ul><li><p>Communicate proactively with internal and external collaborators to resolve distribution customer concerns and issues while maintaining high standards of order fulfillment.</p></li><li><p>Serve as the primary point of contact for vendors and partners; maintain collaboration and ensure adherence to contractual obligations and SLAs.</p></li><li><p>Be responsible for day‑to‑day distribution operations to ensure timely delivery, adherence to schedules, and operational efficiency.</p></li><li><p>Conduct regular vendor performance reviews and prepare quarterly reports for internal leadership and external collaborator presentations.</p></li><li><p>Provide oversight of 3PL activities with regulatory and contractual requirements, including GDP standards.</p></li><li><p>Handle and supervise distribution budgets, balancing cost efficiency with quality service delivery; track variances and drive corrective actions.</p></li><li><p>Track and report distribution metrics such as delivery timelines, inventory levels, and vendor performance; surface insights to guide decisions.</p></li><li><p>Rectify data anomalies using internal dashboards and systems; ensure accurate reporting, detailed data integration, and data integrity.</p></li><li><p>Support contract development, amendments, and compliance in collaboration with Legal and cross‑functional teams.</p></li><li><p>Resolve claims efficiently; establish standard operating procedures and conduct proactive reviews to optimize workflows and reduce recurrence.</p></li><li><p>Develop and maintain policies and procedures that strengthen distribution strategies and vendor relationships.</p></li><li><p>Ensure compliance with trade regulations, GDP standards, and other relevant distribution requirements across the broader EU operations.</p></li><li><p>Collaborate with cross‑functional teams (e.g., Quality, Finance, Customer Service, Supply Chain, Commercial) to implement process improvements aligned to organizational goals.</p></li><li><p>Produce reports and briefing materials for senior management on distribution performance, vendor adherence, and risk/mitigation status.</p></li><li><p>Identify and mitigate risks and dependencies early; recommend pragmatic solutions and secure cross‑functional alignment on course corrections.</p></li></ul><p><strong>This Role Might Be for You If You Have</strong></p><ul><li><p>Hands‑on experience leading distribution operations across Europe, especially ES/FR and Switzerland, with exposure to rare disease or specialty distribution.</p></li><li><p>Vendor and 3PL management expertise, including contract oversight, SLA governance and performance reviews.</p></li><li><p>Strong understanding of GDP, trade regulations, and compliance expectations for pharmaceutical/healthcare distribution in the EU and Switzerland.</p></li><li><p>Data fluency and analytical skills, including dashboarding and KPI reporting</p></li><li><p>Budget management experience with a focus on cost optimization and service quality.</p></li><li><p>Excellent communication and collaborator, adept at handling partner concerns and driving outcomes in a matrixed environment.</p></li><li><p>Process improvement demeanor with experience in standardizing procedures and implementing efficiencies</p></li><li><p>High attention to detail, organization, and follow‑through; ability to balance multiple priorities and deadlines.</p></li><li><p>Willingness to travel to vendor sites, 3PLs, and regional partners as needed.</p></li></ul><p><strong>To Be Considered</strong></p><p>Bachelor’s degree in supply chain or a related field. 6+ years of experience in distribution/trade operations, logistics, or vendor management, with a European focus</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 02:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Meetings and Conventions]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45385]]></requisitionid>
    <referencenumber><![CDATA[R45385]]></referencenumber>
    <apijobid><![CDATA[r45385]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45385/manager-meetings-and-conventions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Meetings, Conventions & Trainings drives detailed delivery of commercial meetings, congresses, and training programs for International Commercial Immunology. Partnering with internal teams, vendors, and alliance collaborators across Europe, Canada, and Japan, you will plan, coordinate, and implement scalable events and trainings that elevate customer engagement and field readiness while ensuring compliance, budget rigor, and measurable impact.</p><p><strong>A Typical Day</strong></p><ul><li><p>Coordinate internal and external collaborators, including global marketing and alliance partners, to align content, logistics, and onsite execution.</p></li><li><p>Handle vendor and venue selection, negotiation, and performance; coordinate contracts, SOWs, and day‑of delivery across AV, catering, exhibits, and attendee services.</p></li><li><p>Own event budgets: build forecasts, track commitments, handle POs and invoices, and reconcile actuals with post‑event reporting.</p></li><li><p>Ensure compliance with company policies and industry codes related to promotional events and HCP interactions; maintain documentation for audit readiness.</p></li><li><p>Lead all aspects of attendee communications, registration, travel, and onsite operations; troubleshoot issues to protect experience, safety, and brand standards.</p></li><li><p>Partner with the International Training Lead to coordinate field training logistics and delivery, ensuring alignment with curriculum, materials, and readiness plans.</p></li><li><p>Maintain standardized SOPs, playbooks, checklists, and templates; drive continuous improvement in planning processes and vendor management.</p></li><li><p>Track and report KPIs and leading indicators for meetings and trainings; synthesize feedback and insights to plan for future planning and budget allocation.</p></li><li><p>Collaborate with IT and enablement teams to use event platforms and data tools; ensure data privacy, consent, and secure handling of attendee data.</p></li><li><p>Surface risks and dependencies early; recommend pragmatic solutions and secure cross‑functional alignment on course corrections.</p></li></ul><p><strong>This Role Might Be for You If You Have</strong></p><ul><li><p>Hands‑on experience planning and delivering congresses and commercial meetings across multiple geographies, ideally in healthcare or pharma.</p></li><li><p>Strong project management skills with the ability to lead multiple concurrent workstreams, deadlines, and partners.</p></li><li><p>Proven vendor and venue management expertise, including contract negotiation, service level oversight, and budget stewardship.</p></li><li><p>Excellent communication and relationship‑building skills; adept at partnering across matrixed and alliance environments.</p></li><li><p>High attention to detail with creative problem‑solving.</p></li><li><p>Proficiency with event management platforms and virtual event tools, plus Microsoft Outlook, Word, PowerPoint, and Excel.</p></li><li><p>Willingness to travel for on‑site event delivery, including occasional evenings and weekends aligned to congress calendars.</p></li></ul><p><strong>To Be Considered</strong></p><p>Bachelor’s degree with 6+ years of professional experience, with at least 3+ years focused on events/congress management in healthcare/pharma preferred. 5+ years’ experience in contracts, sponsorships, and/or project management. Experience across Europe (and ideally Canada and Japan) is advantageous; CMP or similar certification is a plus. Fluency in English; additional languages such as Spanish, German, French, Italian, or Japanese are a plus.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Netherlands]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46247]]></requisitionid>
    <referencenumber><![CDATA[R46247]]></referencenumber>
    <apijobid><![CDATA[r46247]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46247/associate-director-finance-administration-netherlands/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></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>Partnering with country leadership on budgeting, forecasting, and financial planning</li><li>Preparing and presenting forecasts, including actuals versus forecast analysis</li><li>Managing resource planning, including FTE utilisation across cost centres</li><li>Supporting commercial teams with P&L ownership and profitability insights</li><li>Translating epidemiology and commercial data into financial forecasts</li><li>Coordinating with Accounting on revenue accuracy, accruals, and reporting</li><li>Acting as a local finance liaison across Tax, Treasury, and CFO functions</li><li>Ensuring compliance with internal policies and external regulations</li></ul><h3>This Role May Be For You If:</h3><ul><li>You enjoy working closely with senior collaborators to support sound decisions</li><li>You like roles that balance strategic perspective with practical execution</li><li>You are comfortable partnering across commercial, medical, and G&A teams</li><li>You value clear country ownership and accountability</li><li>You enjoy collaborating with global and local finance colleagues</li><li>You are motivated by improving processes and strengthening governance</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>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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Finance & Administration - Italy]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46237]]></requisitionid>
    <referencenumber><![CDATA[R46237]]></referencenumber>
    <apijobid><![CDATA[r46237]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46237/director-finance-administration-italy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Director, Finance & Administration to provide senior finance leadership at country level while contributing to the International Finance leadership team. This role partners closely with country leadership and global CFO functions, shaping financial strategy, governance, and commercial performance while supporting critical business decisions through insight, forecasting, and analysis.</p><p>With visible ownership of country financial outcomes and selected above‑country initiatives, this role combines strategic leadership with hands‑on engagement across Finance, Commercial, Medical, G&A, and corporate teams.</p><h3>What You’ll Be Doing:</h3><ul><li>Acting as senior finance partner to country and site leadership</li><li>Contributing to country and International Finance leadership forums</li><li>Leading budgeting, forecasting, and long‑range financial planning activities</li><li>Owning country‑level commercial P&Ls and profitability outcomes</li><li>Supporting commercial teams through revenue forecasting and GTN analysis</li><li>Translating epidemiology and market data into financial forecasts</li><li>Coordinating resource planning, including headcount and FTE utilisation</li><li>Providing governance oversight across CFO policies and compliance</li><li>Serving as key country liaison with Accounting, Tax, Treasury, and global Finance</li><li>Handling and developing finance professionals and office management teams</li><li>Taking ownership for selected above‑country initiatives and priorities</li></ul><h3>This Role May Be For You If:</h3><ul><li>You enjoy operating as the senior finance voice within a country organisation</li><li>You are comfortable influencing at leadership level across multiple functions</li><li>You value roles with accountability for both strategy and execution</li><li>You enjoy representing local markets within international leadership teams</li><li>You are motivated by strengthening governance, controls, and financial insight</li><li>You like developing people while remaining close to the business</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 ten years of post‑qualification finance experience, primarily within the biotech or pharmaceutical industry, including extensive experience supporting commercial P&Ls. Fluency in English and the local country language is required. Experience operating in international environments and additional language capabilities are an advantage.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Digital Lab Orchestration]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45569]]></requisitionid>
    <referencenumber><![CDATA[R45569]]></referencenumber>
    <apijobid><![CDATA[r45569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45569/associate-director-digital-lab-orchestration/]]></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[<div><p>The Associate Director of Digital Lab Orchestration you will be responsible for leading designing, integrating, and deploying the orchestration layer that connects QC laboratory systems into a cohesive, compliant, and automated ecosystem. This role bridges QC operations, IT/OT, automation, and data governance to enable end-to-end digital QC workflows.</p></div><div><div><div><div><p>As an Associate Director, a typical day might include the following:</p><ul><li>Lead the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Enable automated sample lifecycle management, test execution, result capture, review, and release.</li><li>Support real-time and near-real-time data flow from lab instruments to enterprise systems.</li><li>Assist in annual IT budgeting, vendor negotiations, and resource allocation.</li><li>Ensure integrations comply with GxP, ALCOA+, 21 CFR Part 11, Annex 11 and data integrity requirements.</li><li>Partner with Quality and CSV teams to support validation strategies (risk-based, CSA where applicable).</li><li>Ensure auditability, traceability, and controlled change management.</li><li>Act as the primary integration point between QC, IT, automation, and external vendors.</li><li>Evaluate vendor platforms and integration tools for orchestration capabilities.</li><li>Lead technical discussions with system integrators and software suppliers.</li><li>Support incident resolution, root cause analysis, and continuous improvement.</li><li>Make decisions on integration patterns and drive a connected lab progression in 2026 and beyond</li><li>Ensure resiliency is incorporated into our architecture- as we move into a connected lab platform</li></ul><p>This role may be for you if you have:</p><ul><li>Knowledge of integration technologies: REST APIs, middleware/iPaaS, message brokers, ETL</li><li>Familiarity with orchestration/workflow engines</li><li>Understanding of lab instrument connectivity and data flows</li><li>Experience with cloud and/or hybrid architectures (AWS, Azure, or similar)</li><li>Industry experience implementing Lab orchestration including Scitara, Tetra Science, or any other emerging tools.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and </p><ul><li>Senior Manager: 8+ years industry experience in Information Systems and Technology or equivalent combination of education and experience. 6 of those years should be in managing employees and budgets, with 5+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment.</li><li>Associate Director: 10+ years industry experience in Information Systems and Technology or equivalent combination of education and experience. 8 of those years should be in managing employees and budgets, with 7+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment. </li><li>Experience with IT Compliance guidelines including PICS, CFR21 Part 11, Annex 11 and GAMP preferred.</li></ul></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>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Medical Operations]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46214]]></requisitionid>
    <referencenumber><![CDATA[R46214]]></referencenumber>
    <apijobid><![CDATA[r46214]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46214/senior-manager-medical-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>The Senior Manager, Managed Access Programs will be responsible for all operational aspects of multiple projects/programs such as Expanded Access Programs, individual patient expanded access, and post-trial access managed by Medical Affairs. Based on team assigned, this role may include supervision of staff. Additionally, the incumbent will support other MA projects, as requested.</p><h3>As a Senior Manager, a typical day may include:</h3><h3>Program management activities:</h3><ul><li><p>Has operational responsibility across multiple projects/program(s) with minimal direction: Expanded Access Programs, individual patient expanded access, post-trial access</p></li></ul><h3>Meetings & Committees:</h3><ul><li><p>Participates in team review meetings, product team alignment meetings, and program budget & status update meetings as needed</p></li></ul><h3>Budget Management:</h3><ul><li><p>Accountable for financial forecasting accuracy of Managed Access Programs within span of responsibility</p></li><li><p>Maintenance of program budget trackers for each molecule/activity, ensuring all communicated actuals and accruals are captured, projections are reforested as necessary, and brand give back are fully assessed</p></li><li><p>Maintains financial forecast for programs for quarterly for reporting to Accounting & Finance, and responsible for ensuring issue resolution for all discrepancies</p></li></ul><h3>Drug Supply:</h3><ul><li><p>Responsible for managing drug supply for Expanded Access Programs and individual patient expanded access, as appropriate</p></li></ul><h3>Metrics & Reporting:</h3><ul><li><p>Responsible for ongoing analyses, tracking and reporting of projects/programs support, timelines for completion, expected or assessed delays, solutions for streamlining processes for greater efficiency, and other related metrics in support of program activities</p></li></ul><h3>Vendor Management:</h3><ul><li><p>Manages vendors and financial tracking as required per program</p></li></ul><h3>Essential Documents:</h3><ul><li><p>Ensures appropriate archiving of projects’/programs’ essential documents</p></li></ul><h3>Systems Management:</h3><ul><li><p>Utilizes appropriate systems to contribute to cross-functional communication, planning and transparency, including but not limited to:</p></li><li><p>Ensures ongoing QC of SharePoint document storage for completeness and audit readiness</p></li><li><p>Expertise required in the utilization of QlikSense, QlikView, SharePoint, Oracle and ESRA portal to support team needs</p></li></ul><h3>Process:</h3><ul><li><p>Adheres to all relevant processes, trainings, and SOPS to ensure consistency, efficiency, and compliance. Exercises' judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions; Continued process improvements</p></li></ul><h3>Organizational goals:</h3><ul><li><p>Development of objectives in order to quantify success and attainment of goals. Ensures optimal structure, procedures, and adequate resources supporting growth of multiple projects/programs. Knows when to escalate issues, and involve senior levels of management to obtain adequate resolution</p></li></ul><h3>Alliance Management:</h3><ul><li><p>Ensures financial transparency and alignment with both Alliance and internal stakeholders, supporting the product team financial reviews</p></li></ul><p>To be considered a bachelor’s degree is required and an advanced degree preferred. You are to have 5- 8 years’ experience working in clinical research or medical operations within the pharmaceutical or biotech industry. Active working experience and/or courses pertaining to clinical research and/or MA areas (such as GCP, Investigator Initiated Studies; medical/educational grants administration; medical information; registries; OIG/PhRMA guidance.). Compassionate Use or Managed Access programs preferred. We are seeking strong communication and presentation skills for senior management audiences.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Quantitative Pharmacology]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R38122]]></requisitionid>
    <referencenumber><![CDATA[R38122]]></referencenumber>
    <apijobid><![CDATA[r38122]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r38122/senior-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>We are looking for a Senior Group Director in Quantitative Pharmacology. This individual will be responsible for managing a team functioning in one or more therapeutic focus area. In this capacity the SGD is accountable for the successful and timely completion of QP related activities, encompassing a broad array of deliverables in support of Drug Safety and Pharmacometrics. The successful applicant will support a range of assets from Early Clinical Development through submission and beyond.</p><p><em>This position can be based in our Tarrytown, NY, Warren, NJ or Cambridge, MA offices.</em></p><p><strong>A day in the life of a Senior Group Director may look like:</strong></p><ul><li><p>Managing and mentoring a broad spectrum of individual contributing scientists.</p></li><li><p>Providing technical guidance and mentoring of colleagues within the function and across the organization.</p></li><li><p>Performance management and assessment of staff and providing guidance and training to enable their success.</p></li><li><p>Utilizing a mastery level of PK/PD knowledge and strategic leadership skills, effectively developing and implementing strategic analyses in support of research and development projects.</p></li><li><p>Taking accountability for the PK/PD evaluation of a portfolio of products or projects, and/or highly complex projects that are wide in scope.</p></li><li><p>Identifying opportunity for process and procedural improvements, product or service improvements.</p></li><li><p>Solving unique and complex problems that have a broad impact on the business.</p></li></ul><p><strong>This may be the right role for you, if you:</strong></p><ul><li><p>Can inspire and lead colleagues to deliver PMx and company goals.</p></li><li><p>Want the ability to make a significant impact on the organization and external groups, and can influence and effect change.</p></li><li><p>Enjoy making contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p></li><li><p>Understand long-term career opportunities and can guide other QP staff on potential directions.</p></li></ul><p><strong>In order to be considered qualified for this role, you must have:</strong></p><ul><li><p>10+ years of industry experience (with a Ph.D.) or 12+ years (with an M.S.), focusing on modeling and simulation, PK/PD (pharmacokinetics/pharmacodynamics), systems pharmacology, and quantitative drug development strategies.</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>A proven ability to display excellent interpersonal and communication skills both written and oral and ability to communicate complex information succinctly.</p></li><li><p>Strong collaborative skills and effective at building alliances across functions, as well as the ability to effectively influence colleagues and multi-disciplinary project teams.</p></li><li><p>The ability to handle all types of projects and leverage higher level staff for technical input and brainstorming to implement solutions for complex projects.</p></li><li><p>Proven experience interacting with regulatory agencies without supervision, and within the company to develop regulatory strategy.</p></li></ul><p>#REGNQPCP</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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$238,400.00 - $397,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Neurology Marketing]]></title>
    <date><![CDATA[Thu, 29 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44929]]></requisitionid>
    <referencenumber><![CDATA[R44929]]></referencenumber>
    <apijobid><![CDATA[r44929]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44929/executive-director-neurology-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[<p>The Executive Director, Neurology Marketing, is a member of the newly formed Neurology Business Unit with accountability for leading and shaping commercialization and driving performance of Neurology brands globally, including full responsibility for US strategy and performance. In a complex competitive environment, this leader must critically assess how to optimally launch our first brand in Myasthenia Gravis and continually drive growth and challenge the status quo worldwide.</p><p>The Executive Director, Neurology Marketing, will set the global vision, leading the marketing team. Key responsibilities will include ensuring alignment with commercial imperatives, and driving cross-functional integration across the US & International Teams. The Executive Director, Neurology Marketing, plays a critical role in bringing Regeneron science to Myasthenia Gravis patients and delivering consistent commercial impact.</p><p><strong>In this position a typical day may include the following:</strong></p><ul><li>Leading and inspiring marketing team with US and International HQ marketing team members as well as US field based team members. Establishes trust within the team at all levels, and with cross functional partners. Creates environment for learning agility, developing marketing talent and attracting leaders to the team.</li><li>Establishing and evolving the Neurology strategy to drive differentiation and portfolio value across geographies, balancing US and International market input into global strategy build</li><li>Planning business effectively for global and local market execution, being agile and able to balance/prioritize overall tactical initiatives to build and complete strategy</li><li>Driving and leading global brand planning, able to use critical thinking to develop meaningful brand and asset strategies to increase the value of our Neurology launch brand in Myasthenia Gravis and our ability to get it to patients who can benefit.</li><li>Working in close collaboration with Clinical, Medical Affairs and Field Medical to ensure strategic alignment with Medical Education strategic plans</li><li>Providing strategic input into collaboration with Insights and Data Analytics teams to conduct global market analyses and translate them into clear strategic choices and prioritization globally, ensuring team has insights and data needed to do so</li><li>Representing the commercial in decision-making forums (e.g., Commercial/Clinical cross-functional committees) to influence prioritization, resource allocation, and long-range planning based on scientific & commercial potential</li><li>Managing team of direct reports and their respective teams, ensuring alignment with Global strategy and vision, and providing input/direction into critical activities/initiatives as well as prioritization</li><li>Developing professional relationships and contacts with global physician experts and attends key congresses</li><li>Creating processes and drives initiatives related to commercial launch and marketing efforts, proactively addressing hurdles in oncology asset commercialization where applicable</li><li>Maintaining line of sight to global P&L for Neurology brands across markets and accountable for US P&L</li><li>Ensuring the development, implementation, and administration of marketing processes, programs, and internal reports are consistent with corporate guidance and all regulatory, legal, ethical guidelines</li><li>Supporting team efforts to develop promotional content, including ensuring Medical/Legal/Regulatory Review committee effectiveness</li><li>Managing and developing team members, ensuring their continued development and growth.</li><li>Ensuring that team develops and tracks important metrics to monitor success of promotional activities and refines strategy/tactics based on benchmark outcomes</li><li>Providing consistent reporting of status, future planning, and issues/challenges to VP of Neurology, ensuring alignment with VP and senior leadership on strategic plans</li><li>Working cross functionally to create, manage and track US and Global budget to ensure team is operating within the approved budget and phasing and proactively identifying efficiencies</li></ul><p><strong>This May Be the Right Role for You If you:</strong></p><ul><li>You are analytical and can communicating metrics easily</li><li>You demonstrate strong project and process skills with attention to detail</li><li>You can communicate and act promptly; demonstrated initiative, creativity, and ability to stay agile and work effectively in complex, rapidly changing environments.</li><li>You are proactive and able to prioritize, comfortable leading in ambiguity</li><li>You use interpersonal and presentation skills both internally & externally, as well as other professional/productive behaviors conducive to a productive and positive team environment</li><li>You are a strong people leader</li></ul><h3>To be considered for this role you bring,</h3><ul><li>Bachelor's degree</li><li>15 years of progressive experience in pharmaceutical marketing, brand strategy and execution. Neurology experience is preferred and Myasthenia Gravis or Neurology Rare Disease experience a plus.</li><li>Deep experience in global commercial, marketing, and brand positioning and strategy development for oncology projects in US</li><li>Experience in marketing outside of US markets with an appreciation for high-level access and commercial challenges in those markets/geographic regions</li><li>Exemplary marketing technical skills, ranging from strategy to tactical execution, extensive experience in and understanding of brand management</li><li>Proven track record of market analysis and identifying growth opportunities on a global scale</li><li>Understanding of global to local market trade-offs during global commercialization planning</li><li>Experience leading cross-functional teams within a pharmaceutical or healthcare organization in the US and outside of the US, specifically for Neurology assets</li><li>Track record of adapting strategies based on market access, regulatory, development, and other cross-functional considerations</li><li>Track record of creating and driving initiatives to support global launch planning and marketing, and life cycle management strategy and planning</li><li>Experience in leading and developing long range brand plans, budgets and forecasts within commercial teams in the pharma/biotech industry</li><li>Proficient understanding of Neurology provider treatment environment and economics across academic and community hospitals and clinics, buy & bill, specialty pharmacy, IDNs, PHS hospitals, hospital and system pharmacy, and payers.</li><li>Understanding of rare Neurology therapeutic areas, drug development, & regulatory environment</li><li>Preferred- Prior pharmaceutical sales experience</li><li>Must be willing to travel 25-30% (including weekend and international travel as needed)</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 30 Jan 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44637]]></requisitionid>
    <referencenumber><![CDATA[R44637]]></referencenumber>
    <apijobid><![CDATA[r44637]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44637/associate-director-clinical-scientist-internal-medicine-cardio-metabolic-renal/]]></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 Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director Clinical Sciences, and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3><strong>As an Associate Director, a typical day may include the following: </strong></h3><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical SubTeam</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>Applies proficient scientific expertise to propose, design, and complete 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</p></li><li><p>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>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Applies 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><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><h3>This role may be for you if:</h3><ul><li><p>Ability to lead activities within a matrix environment; 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><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs.</p></li><li><p>Strong cross-functional management, interpersonal and problem-solving skills with a proven track in clinical trial process improvements.</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have ≥ 10 years of pharmaceutical clinical drug development experience. We are seeking experience in managing clinical trials in one or more of the following therapeutic areas – cardiovascular, renal, metabolic disease. Demonstrate proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills. Other levels considered depending on experience. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><p>(1 of 2)</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Délégué(e) Hospitalier(e) Oncologie – Paris]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45224]]></requisitionid>
    <referencenumber><![CDATA[R45224]]></referencenumber>
    <apijobid><![CDATA[r45224]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45224/delegue-e-hospitalier-e-oncologie-paris/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>As an Oncology Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, within your assigned territory - <strong>Paris area</strong>. You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>Oncology Pharmaceutical Representative - Paris</strong></p><p><strong>As an Oncology Pharmaceutical Representative, a typical day might include the following:</strong></p><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><p><strong>This role might be for you if:</strong></p><ul><li>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</li><li>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</li><li>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</li><li>You can operate effectively in a “start-up” model as this is a completely new team.</li></ul><p>To be considered for this opportunity you must hold a Carte Professionnelle with minimum <strong>5+ years of pharmaceutical sales experience in Oncology</strong>. You are happy with regular travel and have a valid driver's license. Conversational English would be desirable, but not required</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Feb 2026 05:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist-Atlanta, GA]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44968]]></requisitionid>
    <referencenumber><![CDATA[R44968]]></referencenumber>
    <apijobid><![CDATA[r44968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44968/oncology-account-specialist-atlanta-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[<p><strong>Geography: Atlanta, GA</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><h3><strong>A typical day may include the following:</strong></h3><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><h3><strong>This role might be for you if: </strong></h3><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 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). 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. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. 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. 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><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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Feb 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Market Access DACH (f/m/d)]]></title>
    <date><![CDATA[Sat, 14 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45066]]></requisitionid>
    <referencenumber><![CDATA[R45066]]></referencenumber>
    <apijobid><![CDATA[r45066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45066/senior-manager-market-access-dach-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>Diese Rolle wurde geschaffen, um die End‑to‑End‑Steuerung von HTA‑Einreichungen sowie Preisverhandlungen in Deutschland, der Schweiz und Österreich für ausgewählte Produkte und Indikationen zu übernehmen. Dabei stellst du sicher, dass die strategische Ausrichtung eng und zeitgerecht mit den lokalen und globalen Teams abgestimmt ist.</p><p>Als <strong>Senior Manager Market Access (w/m/d)</strong> steuerst du funktionsübergreifende Beiträge zur Einreichungs‑ und Verhandlungsstrategie sowohl mit medizinischen und kommerziellen Teams auf Länderebene als auch mit Market‑Access‑ und Pricing‑Teams auf globaler Ebene.</p><h3><strong>Deine Aufgaben:</strong></h3><ul><li><p>Zusammenarbeit mit globalen und lokalen Market‑Access‑Leads, um qualitativ hochwertige und fristgerechte HTA‑Einreichungen für Deutschland, die Schweiz und Österreich sicherzustellen</p></li><li><p>Analyse von Daten zu G‑BA‑Nutzenbewertung, Zugang, Preisgestaltung, Vertragsmodellen und Markenperformance</p></li><li><p>Entwicklung und Abstimmung einer Market‑Access‑ und Pricing‑Strategie gemeinsam mit den Commercial Teams der Länder</p></li><li><p>Identifikation und Kommunikation relevanter Anforderungen der Kostenträger an lokale Market‑Access‑, HEOR‑ und/oder Medical‑Affairs‑Teams zur Unterstützung der Evidenzgenerierung und Value Dossiers</p></li><li><p>Mitwirkung an der strategischen Preisfindung auf globaler Ebene sowie Unterstützung bei lokalen Preisverhandlungen; Identifikation innovativer Lösungen für Market Access, z. B. neue Preis‑/Vertragsmodelle</p></li><li><p>Unterstützung der Länderorganisationen beim Aufbau und der Umsetzung geeigneter Market‑Access‑Pläne unter Berücksichtigung lokaler Rahmenbedingungen</p></li><li><p>Beitrag zur Bewertung neuer Indikationen oder Produkte, inkl. Potenzialanalyse, Value Story und regulatorischen Aspekten</p></li><li><p>Vorbereitung und Entwicklung relevanter KPIs und Analysen zur Unterstützung länderspezifischer Preisüberprüfungen</p></li></ul><br><h3><strong>Das bringst du mit:</strong></h3><ul><li><p>Erfahrung im Bereich Market Access in der pharmazeutischen Industrie; gerne in einem multidisziplinären, matrixorientierten und internationalen Umfeld</p></li><li><p>Erfahrung in der Erstellung und Einreichung von HTA‑Dossiers</p></li><li><p>Erfolge in der Entwicklung und Umsetzung von Market‑Access‑Strategien</p></li><li><p>Erfahrung in der Erstellung überzeugender Value Propositions und Zugangskonzepte</p></li><li><p>Nachweisbare Beiträge zur erfolgreichen Preisumsetzung</p></li><li><p>Erfahrung im Aufbau von KPIs, Dashboards und Analyseinstrumenten</p></li></ul><br><h3><strong>Deine Qualifikationen:</strong></h3><ul><li><p>Mindestens 5 Jahre Berufserfahrung im Bereich Market Access in der pharmazeutischen Industrie</p></li><li><p>Fundierte Kenntnisse der deutschen, österreichischen und schweizerischen Gesundheits- und Erstattungssysteme sowie Erfahrung in Verhandlungen mit Behörden und Kostenträgern</p></li><li><p>Wünschenswert: Expertise im Bereich Onkologie</p></li><li><p>Erfahrung in der Zusammenarbeit in einem internationalen Umfeld</p></li><li><p>Ein postgraduales Studium (z. B. MBA, MSc oder vergleichbar) ist von Vorteil</p></li><li><p>Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift</p></li></ul></div></div><p>Sehen Sie sich selbst in dieser Stellenbeschreibung? Dann bewerben Sie sich jetzt und machen Sie den ersten Schritt in Richtung „Regeneron Way“! Wir haben eine inklusive Kultur, die umfangreiche Sozialleistungen bietet, die je nach Standort variieren. In den USA können die Leistungen Gesundheits- und Wellnessprogramme (einschließlich Krankenversicherung, Zahn-, Sehkraft-, Lebens- und Berufsunfähigkeitsversicherung), 401(k)-Zusatz des Unternehmens, Familienleistungen, Aktienzuteilung, bezahlte Freistellungen und bezahlten Urlaub (z. B. Militär- und Elternzeit), für berechtigte Mitarbeiter auf allen Ebenen umfassen! Für weitere Informationen über die Leistungen von Regeneron in den USA siehe https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. Für die spezifischen Vorteile anderer Länder sprechen Sie bitte mit Ihrem Personalberater.<br>Wir sind der Meinung, dass wir bei Regeneron am erfolgreichsten sind und am besten arbeiten, wenn wir zusammen sind. Aus diesem Grund sind viele Aufgaben bei Regeneron nur vor Ort zu erfüllen. Bitte wenden Sie sich an Ihren Personalberater und Personalverantwortlichen, um weitere Informationen über die Vor-Ort-Richtlinien von Regeneron und über die Erwartungen für Ihre Rolle und Ihren Standort zu erhalten.<br> </p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 14 Feb 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Procurement - Direct (Chemicals Category)]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41123]]></requisitionid>
    <referencenumber><![CDATA[R41123]]></referencenumber>
    <apijobid><![CDATA[r41123]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41123/director-global-procurement-direct-chemicals-category/]]></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>Regeneron is seeking a Director, Global Procurement - Direct / Chemicals, with experience in end-to-end procurement strategies/processes and with proven successful global category execution in Raw Materials and Manufacturing Operations. Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led for 36 years by physician-scientists, Regeneron's unique ability to translate science repeatedly and consistently into medicine has led to numerous FDA-approved treatments and products in development, almost all of which were homegrown in Regeneron's laboratories.</p><p><strong>As the Director, Global Procurement - Chemicals a typical day may include:</strong></p><ul><li>Leading, defining, and implementing the global Raw Material / Chemicals Category strategy to serve global and regional business needs. Category may include Chemicals and/or other Raw Materials.</li><li>Manage a team of professional level employees responsible for performing category management tasks. Provide coaching and guidance on job performance and career development to direct reports.</li><li>Working closely with internal & external partners to lead discussions related to the Raw Material Categories and aligning the category priorities.</li><li>Leading negotiations, supplier management activities, and stakeholder engagement activities.</li><li>Driving value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</li><li>Representing Global Procurement by participating in organizational decisions in the Raw Material categories with critical short and long-term impact on the success, efficiency, growth, and results of the organization and company.</li><li>Leads category activities to ensure compliance with appropriate GxPs and other applicable regulations and proficiency on procurement technical skills among global procurement team.</li></ul><p><strong>This role might be right for you if you have:</strong></p><ul><li>Demonstrated knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support growth and evolution of programs as well as the knowledge to drive improvement across the category</li><li>Experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</li><li>Expertise in developing influential relationships with stakeholders and suppliers.</li><li>Led cross-functional teams to drive results in Raw Material categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</li><li>Expert insights and knowledge regarding rates, unit costs, and costing structures to enable optimal negotiations.</li><li>Ability to leverage external data sources, market information, and supplier engagement to constantly improve the intelligence / analytics of supply market dynamics.</li><li>Operate with integrity, focus, and clarity in an environment of ambiguity to drive change and improvement.</li></ul><p><strong>To be considered for this role you must possess </strong><strong>a bachelor's degree in a relevant field of study plus 15+ years of progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma. </strong><strong>Experience leading manager level professionals in a multi-national firm including writing performance reviews, setting annual objectives, coaching, and developing direct reports. Working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other) Ability to leverage standard business applications for communicating, presenting and analyzing (i.e. Word, Excel, PowerPoint)</strong></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>$169,600.00 - $282,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 06:56:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Global Procurement - Facilities, Capital, and Logistics]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44897]]></requisitionid>
    <referencenumber><![CDATA[R44897]]></referencenumber>
    <apijobid><![CDATA[r44897]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44897/senior-director-global-procurement-facilities-capital-and-logistics/]]></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>We are currently looking to fill a Senior Director Global Procurement, Facilities, Capital and Logistics position within our team. In this role you will be responsible for leading, defining and implementing the Global Facilities, Capital, and Logistics Category strategy to serve global and regional business needs. As an Sr Director you will work closely with stakeholders to lead discussions related to the Facilities, Capital, and Logistics Categories and aligns category priorities with procurement management</p><p>In this role, a typical day may include the following:</p><ul><li><p>Leads negotiations, supplier management activities, and stakeholder engagement activities for the Facilities, Capital, and Logistics Category as assigned.</p></li><li><p>Works independently to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Represents Global Procurement by participating in organizational decisions in the Facilities, Capital, and Logistics categories with critical short and long-term impact on the success, efficiency, growth, and results of the organization and company.</p></li><li><p>Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Leads category activities to ensure compliance with appropriate GxPs and other applicable regulations.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li><li><p>Provides coaching and guidance on job performance and career development to direct reports and provides leadership examples for the organization.</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li></ul><p>This role may be a fit for you if you:</p><ul><li><p>Have experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</p></li><li><p>Can build influential relationships with stakeholders and suppliers to drive results for Regeneron.</p></li><li><p>Can provide expert insight and knowledge regarding rates, unit costs, and costing structures to enable optimal negotiations.</p></li><li><p>Have used external data sources, market information, and supplier engagement to constantly improve Regeneron’s knowledge of supply market dynamics.</p></li><li><p>Can demonstrate success leading and directing the global supply market evaluation process using all available market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Has experience leading professionals in a multi-national firm including writing performance reviews, setting annual objectives, coaching, and developing direct reports.</p></li><li><p>Has working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Has ability to leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Powerpoint)</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><ul><li><p>Sr Director level: 15+ years of experience in relevant functions or industries. The ideal candidate will have in-depth knowledge of success leading cross-functional teams to drive results in Facilities, Capital, and Logistics categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</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>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 10:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-North, GA (Huntsville, AL - Rome, GA - Alpharetta, GA)]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45002]]></requisitionid>
    <referencenumber><![CDATA[R45002]]></referencenumber>
    <apijobid><![CDATA[r45002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45002/medical-specialist-i-dermatology-north-ga-huntsville-al-rome-ga-alpharetta-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Huntsville]]></city>
    <state><![CDATA[Alabama]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: North GA</strong></p><p><strong>Territory Includes: Huntsville, AL - Rome, GA - Alpharetta, GA</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) – Dermatology Mie Area]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45285]]></requisitionid>
    <referencenumber><![CDATA[R45285]]></referencenumber>
    <apijobid><![CDATA[r45285]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45285/medical-representative-mr-dermatology-mie-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Assigned Area: </strong></p><p>You will primarily work in the Mie area. </p><p>Your residence is expected to be in Mie or Nagoya. </p><p><strong>Job Overview: </strong></p><p>While embodying Regeneron’s philosophy of "putting patients first," you will play a key role in the Immunology Department's dermatology division by managing Dupixent and achieving sales targets. </p><p>Utilizing excellent business acumen and strategic thinking, you will aim to achieve and exceed corporate goals by building trust-based relationships with customers and offering valuable solutions. </p><p><strong>Main Responsibilities: </strong></p><p>- Budget and expense management to achieve brand sales targets </p><p>- Developing and implementing annual business plans using market insights </p><p>- Building strategic sales plans based on key data </p><p>- Performing various administrative tasks (e.g., expense reporting, marketing reports) </p><p>- Compliance with regulations and legal requirements </p><p>- Participation in area meetings and nationwide conferences </p><p>- Completion of training programs and skill development </p><p>- Travel as needed (including nights and weekends) </p><p>- Conducting business safely while driving </p><p><strong>Required Skills and Experience: </strong></p><p>- Sales experience targeting university hospitals </p><p>- Specialized knowledge in dermatology and sales experience with biologics </p><p>- Excellent customer engagement and communication skills </p><p>- Strategic thinking and ability to work independently </p><p>- Proficiency in IT and digital tools </p><p>- Experience in joint promotions with alliance companies </p><p><strong>Preferred Qualifications: </strong></p><p>- Clinical knowledge of competitive brands or therapeutic areas </p><p>- Network with key opinion leaders in dermatology </p><p>- English proficiency is a plus </p><p><strong>Eligibility: </strong></p><p>- Bachelor’s degree (or equivalent qualification) </p><p>- Over 5 years of sales experience in the pharmaceutical industry </p><p>- MR certification and a valid driver’s license </p><p><strong>Advance Your Career to the Next Level: </strong></p><p>Regeneron provides an environment where every employee can maximize their potential. This is a rewarding position that allows you to leverage your expertise in the dermatology field to deliver significant value to patients and healthcare professionals. This challenge offers an opportunity to elevate your career to new heights.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 02:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs (Oncology)]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45251]]></requisitionid>
    <referencenumber><![CDATA[R45251]]></referencenumber>
    <apijobid><![CDATA[r45251]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45251/medical-director-medical-affairs-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>The US Medical Director of Medical Affairs is responsible for the development of medical strategy, planning & execution of medical affairs activities. We provide scientific/medical leadership by understanding malignant Oncology (solid tumors). You will represent US Medical Affairs for our skin cancer program at cross-functional meetings, aligning and working collaboratively with the Headquarters Medical Affairs Medical Directors and other Medical Affairs functions. </p><p>This position will require you to be on-site 4 days/week at our Sleepy Hollow, NY offices. We cannot offer a remote option. If eligible, we can offer relocation benefits. Your travel days do include days in the office.</p><p><strong>A typical day may include the following: </strong><br>• Defines US specific Oncology strategy, sets annual goals and ensures compliant execution of medical affairs activities. <br>• Collaborate with field medical, providing support to clinical development and clinical research conducted such as the identiﬁcation of medical centers of excellence and key investigators/sites. <br>• Participate in US scientific engagement with external communities advancing scientific and medical understanding including the appropriate development and use of our medicines, the management of disease, and patient care. <br>• Develops the medical strategy and content for local congresses, symposia, advisory boards and local engagements and facilitates and implements such activities. <br>• Delivers scientific presentations to diverse audiences in local cooperative meetings, advisory boards and scientific engagement forums. <br>• Provides appropriate medical input, while maintaining scientific integrity, to commercialization strategies in country and serves as the local medical representative at Global Commercialization teams. <br>• Will act as a lead medical reviewer in the MRC for the local review and approval of promotional, educational and related materials ensuring medical/ scientific accuracy and fair and balanced representation. <br>• Provides medical and scientific review to US IIS proposals, protocols and concepts during the monthly meetings. <br>• Supports and reviews US specific pathways and clinical guidelines submission. </p><p><strong>This may be for you if you: </strong><br>• Can demonstrate effective medical communication skills. <br>• Have a thorough understanding of the US healthcare environment. <br>• Have been accountabilities for evidence generation, external engagement and internal advice within a Medical Affairs function<br>• Ability to lead business and technical discussions internally and externally and explain scientific/medical concepts to all levels.</p><p>To be considered you are to be a Healthcare professional with a PharmD, PhD, or equivalent (a physician/MD is preferred.) Expertise in Oncology (solid tumors) clinical, research and/or drug-development is required. Minimum of +7 years’ experience in the pharmaceutical industry and medical affairs is required. Ability and willingness to travel ~40% of the time with some international travel. <br> </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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Production / Manufacturing Operations]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45601]]></requisitionid>
    <referencenumber><![CDATA[R45601]]></referencenumber>
    <apijobid><![CDATA[r45601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45601/production-manufacturing-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div>Within this role you will be working as part of the Manufacturing Team you will be performing tasks to support the manufacturing operations of both clinical and commercial manufacturing programs at Regeneron Ireland.</div></div></div><div><div><div><div><p><strong>Working a shift pattern in a fully gowned, cleanroom environment, a typical shift might include, but is not limited to, the following:</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>This role might be for you if:</strong></p><ul><li><p>You enjoy working in a team that brings out the best in each other</p></li><li><p>You like tackling problems that need solving, using your verbal and written communication skills to ask questions and adapt quickly</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>To be considered for this opportunity you must have a 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><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><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 / Car Valet</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>#IREADV #JOBSIEST #LI-Onsite #REGNIEEC #REGNIELSM</p></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Rheumatology]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45255]]></requisitionid>
    <referencenumber><![CDATA[R45255]]></referencenumber>
    <apijobid><![CDATA[r45255]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45255/medical-director-clinical-development-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[<div>The Medical Director, Clinical Sciences is responsible for facilitating assigned studies, providing investigator support of Regeneron driven studies, and may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into the Clinical Program Lead, Clinical Sciences and is expected to have proficient knowledge of the drug development process, good clinical practice, study design and research methodology as well as understand Regulatory and compliance landscape in the pharmaceutical industry. This role utilizes scientific and clinical expertise to initiate, propose, design and execute research and development programs for early and/or late stage assets for rheumatology/autoimmunity indications. This role may be suitable for an Rheumatologist, Allergist, Immunologist, Pulmonologist, or Dermatologist with industry experience. Clinical research experience in the academic/clinical setting may be considered at the Medical Director level.</div><div></div><div><div><div><div><p>A typical day in the life may include the following responsibilities:</p><ul><li>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program. Clinical deliverables may include individual protocols; clinical components of regulatory documents/registration dossier and brand related medical information, clinical communication and publications</li><li>Demonstrated ability to influence team and may influence across function</li><li>Ability to lead activities within a matrix environment</li><li>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally</li><li>Advanced analytical and influencing skills</li><li>Ability to communicate concise and clear messages</li><li>Seeks to understand different perspectives and cultures and values differing points of view</li><li>Can identify critical risks and mitigation</li><li>Proficient medical writing skills and advanced presentation skills</li></ul><p>This role may be for you if:</p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p>In order to be considered for this role, a M.D. degree or equivalent is required. Specialized clinical fellowship training in Rheumatology, Allergy, Immunology, Pulmonology, or Dermatology is strongly preferred. 1-4 years of industry experience in clinical development is preferred. Clinical Research experience in the academic/clinical setting may be considered at the Medical Director level.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p></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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 16:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Sustaining Engineering]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44518]]></requisitionid>
    <referencenumber><![CDATA[R44518]]></referencenumber>
    <apijobid><![CDATA[r44518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44518/manager-sustaining-engineering/]]></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 an experienced and strategic Combination Products Sustaining Engineer to manage a team in addition to monitor, investigate, maintain and/or improve the quality and performance of commercial combination products. They will provide comprehensive leadership in engineering product management, regulatory compliance (design controls), and cross-functional collaboration with internal and external stakeholders, for the maintenance of commercial products.</p><p>A typical day for a Manager Sustaining Engineering might include:</p><ul><li><p>Implementing design changes to improve the quality of existing products and/or the customer experience.</p></li><li><p>Assisting with customer complaint investigations to identify root cause.</p></li><li><p>Performing design change assessments for changes to existing products.</p></li><li><p>Maintaining Risk Management Files for existing products based on post marketing surveillance and manufacturing events.</p></li><li><p>Facilitating design transfer of existing products to new manufacturing sites.</p></li><li><p>Performing technical evaluations related to supplier and manufacturing changes.</p></li><li><p>Integrating identified product performance enhancements to new product development.</p></li><li><p>Providing technical guidance to sustaining engineers.</p></li><li><p>Participating in cross-functional design teams to address design issues.</p></li><li><p>Developing and maintaining key business partner relationships throughout Regeneron.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Understand relevant FDA regulations, particularly 21 CFR Part 3 and 21 CFR 820.30.</p></li><li><p>Have experience with design history file management (21 CFR 820.30).</p></li><li><p>Possess strong project management and interpersonal skills and strong analytical and problem-solving capabilities.</p></li><li><p>Can balance business objectives with technical constraints.</p></li><li><p>Can work effectively across multiple functional teams.</p></li><li><p>Seek out continuous improvements and collaborative opportunities to improve internal processes and stakeholder relationships.</p></li><li><p>Have strong technical writing and oral communication skills.</p></li><li><p>Targeted to have direct reports within the Sustaining Engineering organization, to support multiple combination products in commercial distribution.</p></li></ul><p>To be considered for the Manager Sustaining Engineering you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a B.S in Engineering; Biomedical Engineering, Mechanical Engineering, Industrial Engineering is preferred.. For various levels you must have the following:</p><ul><li><p>Associate Manager Sustaining Engineering: 6+years of relevant experience </p></li><li><p>Manager Sustaining Engineering: 7+ years of relevant experience</p></li></ul><p>Previous experience in manufacturing of medical devices and/or combination products is preferred. Previous supervisory/ people leadership experience is required. Level is determined based on qualifications relevant to the role.</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>$103,300.00 - $197,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Internal Auditor]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45138]]></requisitionid>
    <referencenumber><![CDATA[R45138]]></referencenumber>
    <apijobid><![CDATA[r45138]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45138/senior-internal-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>Under the direction of the Internal Audit management, the Senior Internal Auditor is responsible for the execution the annual risk-based audit plan that identify value-added recommendations to enhance Company processes and controls. The Senior Auditor will audit the Company’s operations, strategic initiatives, critical business processes and key third-party outsourcing arrangements, as well as participate in the annual Sarbanes-Oxley (SOX) audit of internal controls over financial reporting. This individual will need to have the ability to manage relationships with middle management and work in a highly autonomous manner.</p><p><strong>In this role, a typical day might include the following:</strong> </p><ul><li><p>Under the direction of Internal Audit management, independently review processes and functions as authorized in the approved annual audit plan.</p></li><li><p>Participate in the development of risk-based audit programs and related planning documents for audits.</p></li><li><p>Responsible for the execution of assigned audit sections with little supervision.</p></li><li><p>Conduct audits consistent with IIA practices and in accordance with internal policies and procedures. Additionally, ensure timely completion of assigned testing areas.</p></li><li><p>Identify weaknesses in compliance-related exposures, operational processes and internal controls.</p></li></ul><p><strong>This role might be for you if have experience with :</strong></p><ul><li><p>Promoting internal control practices within the Company by providing internal control expertise as needed to any functions or departments requesting guidance.</p></li><li><p>Identify opportunities to enhance operational efficiencies.</p></li><li><p>Interact autonomously with middle management.</p></li><li><p>Take a lead role in closing meeting with auditees by presenting the findings and related recommendations identified by him/her.</p></li><li><p>Assist Internal Audit management in preparing draft recommendations and audit reports for Senior Management and Audit Committee.</p></li><li><p>Contribute to the Company’s SOX 404 compliance program by completing process review and test of controls as assigned by Internal Audit management.</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><div><ul><li><p>A Bachelor's degree in a relevant field, CPA/CIA certifications preferred </p></li></ul></div><div><ul><li><p>At least 3 years of relevant experience</p></li></ul></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>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, GMP Logistics Systems & Automation]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43650]]></requisitionid>
    <referencenumber><![CDATA[R43650]]></referencenumber>
    <apijobid><![CDATA[r43650]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43650/senior-manager-gmp-logistics-systems-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>The Senior Manager, GMP Logistics Systems and Automation – Automated Warehouse will lead the strategic development, validation, and lifecycle management of logistics systems and mechanical automated warehouse technologies across Global Logistics operations. Ensure end-to-end compliance for warehousing, material flow, and data integrity while delivering safe, efficient, and audit-ready operations integrated with Oracle-based platforms and related enterprise systems.</p><p>As a Senior Manager, a typical day might include the following:</p><ul><li>Serve as a key leader for the design, qualification, and continuous improvement of logistics systems, with emphasis on mechanical automated warehouse equipment and Oracle-based WMS/WES/TMS platforms.</li><li>Own GxP compliance for warehouse systems and processes, aligning with GMP/GDP, GAMP 5 guidance, 21 CFR Part 11/EU Annex 11 for computerized systems, and Annex 15 for qualification.</li><li>Oversee automation projects and ongoing performance of material handling systems to improve throughput, accuracy, and safety while maintaining validated state and robust change control.</li><li>Ensure maintenance of appropriate data integrity controls (ALCOA+), including secure access, audit trails, backup/restore, disaster recovery, and cybersecurity considerations across IT/OT boundaries.</li><li>Ensure GDP-compliant receiving, storage, and distribution processes, including environmental monitoring, temperature mapping, calibration/maintenance, and controlled material flows for sensitive products.</li><li>Lead a cross-functional continuous improvement program that integrates quality-by-design, Lean/Six Sigma, and ICH Q9 risk management principles without compromising validated state.</li><li>Develop and maintain GxP documentation: SOPs, work instructions, validation packages, training curricula, user manuals, and change control records; ensure training completion and effectiveness.</li><li>Partner with Quality, IT, Engineering, EHS, and vendors to troubleshoot, enhance, and sustain system functionality; establish and manage supplier quality expectations and quality agreements.</li><li>Own change control for system and automation upgrades, ensuring impact assessments, validation plans, execution, and release approvals are completed per QMS requirements.</li><li>Monitor and report operational and quality KPIs (e.g., order accuracy, system uptime, deviation/CAPA trends, audit findings, on-time training).</li><li>Provide leadership, coaching, and development to direct reports and project teams, building GxP and automation competencies across global sites.</li><li>Perform other logistics-related tasks as needed to support business continuity and compliance objectives.</li></ul><ul></ul><p>This role may be for you if you have:</p><ul><li>Deep understanding of logistics systems architecture and integration, especially Oracle-based platforms and interfaces to WES/WCS/PLC/SCADA.</li><li>Working knowledge of mechanical automated warehouse systems and their maintenance in a validated state, including calibration, PM/CM, and spare parts strategies.</li><li>Strong command of GxP frameworks: GMP/GDP/GEP, GAMP 5, 21 CFR Part 11, EU Annex 11, Annex 15, and ICH Q9 risk management; practical application of ALCOA+ data integrity.</li><li>Strong project management skills for cross-functional initiatives in fast-paced, multi-site environments; ability to balance operational reliability with improvement.</li><li>Excellent analytical and problem-solving skills; comfort with data analysis, dashboards, and reporting for operational and quality metrics.</li><li>Effective communication and stakeholder management skills across Quality, IT, Operations, Engineering, and external vendors.</li><li>Familiarity with emerging logistics automation technologies (robotics, IoT, AI/ML for predictive maintenance) and cybersecurity considerations for OT/IT convergence.</li><li>Proficiency with Microsoft applications (Excel, Teams, SharePoint) and standard productivity tools.</li><li>Ability to manage multiple priorities, contribute as a collaborative team member, and facilitate meetings and trainings in a global setting.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in Supply Chain Management, Logistics, Engineering, or related field and</p><ul><li>Manager: 7 years of experience in logistics, supply chain systems, or operations management.</li><li>Senior Manager: 8 years of experience in logistics, supply chain systems, or operations management.</li><li>Preferred degrees & certifications: Advanced Degrees, Project Management Professional (PMP), APICS.</li><li>Experience in regulated industries, preferably life sciences or similar environments.</li><li>May consider an equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</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>$108,000.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 05:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Culture and Future of Work]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R40127]]></requisitionid>
    <referencenumber><![CDATA[R40127]]></referencenumber>
    <apijobid><![CDATA[r40127]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r40127/senior-manager-culture-and-future-of-work/]]></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>We are seeking a forward-thinking Senior Manager, Culture & Future of Work to shape how our people, culture, and technology come together to drive the next era of innovation at Regeneron. This role is at the intersection of employee experience, organizational culture, and technology enablement, ensuring that we stay future-ready while keeping human connection at the center of how we work. </p><p>You will blend strategy, research and design to help translate emerging insights into real, tested solutions that enhance how teams collaborate, innovate, and thrive. This is an opportunity to help define the Future of Work in a science-driven, innovation-focused company. You’ll lead initiatives that bring together culture, engagement, and technology to create a better workplace that fuels better science and a better world</p><p><em><strong>This role will require 4 days per week onsite at our Corporate HQ Campus in Sleepy Hollow, NY. This is not available as a fully remote / hybrid work.</strong></em></p></div><div><p><strong>A typical day may include: </strong></p></div><div><ul><li>Design and scale new ways of working that strengthen collaboration, belonging, agility and innovation using facilitation and experimentation to test and refine new work practices</li><li>Lead culture and engagement initiatives that connect purpose and innovation across teams ensuring that inclusion, trust and scientific excellence are built into every experience</li><li>Partner with HR, IT, and business leaders to research and recommend digital and AI-enabled tools for daily work to enhance productivity and employee experience</li><li>Partner with L&LD, Talent Management, and IT and HR technology teams to build Future of Work readiness initiatives, including digital fluency, AI awareness, and workforce upskilling aligned to future skill needs.</li><li>Act as a facilitator, program designer and researcher, bringing structure to complex challenges through workshops, sprints and collaboration design sessions</li><li>Conduct internal and external research on emerging Future of Work trends and translate insights into actionable strategies, frameworks and playbooks</li><li>Serve as a change leader and trusted advisor, helping teams adapt to evolving work models with confidence.</li></ul></div><div></div><div><p><strong>This role may be for you if you have:</strong></p><ul><li>Demonstrated success driving enterprise-level culture and engagement programs and / or introducing digital collaboration tools or AI solutions.</li><li>Strong facilitation and stakeholder engagement skills, including with executive leaders and scientists. </li><li>A deep curiosity about how technology and culture intersect, with a passion for building inclusive, human-centered workplaces enabled by technology</li><li>Experience building and designing culture workshops </li><li>Experience leading inclusive innovation or culture of learning initiatives</li><li>Ability to balance strategic vision with operational execution</li></ul><p><strong>To be considered for this role you must possess a Bachelor’s degree, MBA or Master’s degree in Human Resources or related areas with 8-10 years of progressive experience in organizational development, workforce strategy, employee expereince or related —preferably in biotech or a science-driven sector. </strong></p></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>$132,400.00 - $216,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regulatory Affairs Strategy - Cardiovascular/Metabolic]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45747]]></requisitionid>
    <referencenumber><![CDATA[R45747]]></referencenumber>
    <apijobid><![CDATA[r45747]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45747/director-regulatory-affairs-strategy-cardiovascularmetabolic/]]></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 Regulatory Affairs Strategy will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities will include support to some clinical study activities. The candidate will also supply, lead and/or supervise IND/CTA and BLA submissions activities.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide interpretation of regulatory authorities’ feedback, policies and guidelines.</p></li><li><p>Lead the development of regulatory strategic plans either directly in conjunction with project teams or through your reports. Own the preparation of major clinical submissions required for regulatory approval.</p></li><li><p>Work with project teams to resolve complex project issues. Utilize regulatory expertise and knowledge of regulatory requirements and regulations to strategically interpret, plan, and communicate requirements to ensure attainment of governmental approvals.</p></li><li><p>Responsible for quality and timeliness of IND/CTA and BLA submissions. Interact with other functions and partners, in the preparation, review, and completion of documents for regulatory submissions.</p></li><li><p>Successfully plan, prioritize, supervise and/or conduct activities in close collaboration with leads from other areas. Assure compliance with regulations and with project team timelines.</p></li><li><p>Provide interpersonal support and lead personnel.</p></li><li><p>Critical thinking, leadership skills, assertiveness, excellent negotiation and project management skills as evidenced by past performance on drug development project teams</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>If you bring strong 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><p><strong>To be considered,</strong> you must possess excellent written and verbal communication skills along with a MD, Ph.D. or Pharm D. degree. We expect a minimum of 10 years of pharmaceutical industry experience, at least 7 of which should include regulatory experience.</p><p><em>This role requires you to work onsite 4 days per week in either Warren, NJ or Tarrytown, NY. If you are not local and qualify we can offer relocation support. </em></p><p>#MDJOBSRA #GDRAJobs</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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Fri, 06 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43992]]></requisitionid>
    <referencenumber><![CDATA[R43992]]></referencenumber>
    <apijobid><![CDATA[r43992]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43992/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[<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><p><strong>As a Sr Project Engineer, a typical day might include the following: </strong></p><ul><li>Designing and specifying cGMP process equipment, piping, and controls</li><li>Managing small-to-mid-sized projects related to process equipment and manufacturing</li><li>Assisting in the design review, site acceptance, and installation of equipment</li><li>Preparing piping and instrumentation diagrams (P&IDs) and other related drawings</li><li>Developing Process Flow Diagrams (PFDs) for manufacturing processes</li><li>Supporting the QA Validation department by preparing design documents and assisting in protocol execution</li><li>Reviewing and approving lifecycle documentation, cleaning validation protocols, and summary reports</li><li>Assisting with investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</li><li>Assisting management with tracking of department throughput and efficiency</li><li>Representing the engineering department at cross-functional meetings</li><li>Supervising direct reports as needed</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations and test plans, and executing change control documentation</li><li>Supervising mechanical, electrical, and automation contractors as needed</li><li>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</li><li>Maintaining company reputation by ensuring compliance with all relevant laws, policies, and regulations</li></ul><ul></ul><p><strong>This role may be for you if:</strong></p><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><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><p>#LI-Onsite #JOBSIEPR #IRELIM #REGNIRLTO</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 05:26:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor, Vivarium Operations - Cage Wash]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45952]]></requisitionid>
    <referencenumber><![CDATA[R45952]]></referencenumber>
    <apijobid><![CDATA[r45952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45952/supervisor-vivarium-operations-cage-wash/]]></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 Velocigene team is seeking a <strong>Cage Wash Supervisor </strong>to join their innovative and collaborative group. This position reports directly to the Cage Wash Manager. As Cage Wash Supervisor you will assist management in the daily operation of the Regeneron Vivarium’s cage wash and loading dock operations. Ensuring all caging and equipment are sanitized and processed according to regulatory standards and internal SOPs. This position is also responsible for the basic oversight and support of waste streams, supply receipt, inventory maintenance and multiple areas associate with dirty-side operations.</p><p>You will act as a liaison with animal care staff, management, EHS and Facilities to provide support and ensure all areas of the cage wash and loading dock are properly maintained and running smoothly.</p><p><strong>A Typical Day in the Role Might Look Like: </strong></p><ul><li>Oversee daily operations, including the processing of caging materials, autoclaving supplies, routine maintenance of machines and staff oversight.</li><li>Schedule, train, mentor, and evaluate cage wash personnel.</li><li>Perform daily quality assurance checks and document results. Able to address or report all deviations in a timely manner.</li><li>Assist management in creating weekly schedules and filling service requests. </li><li>Ensure adequate staffing and coverage for all shifts and assist when needed.</li><li>Understand and follow all policies and procedures to ensure compliance with state, local and federal agencies, including adherence to the “Guide for the Care and Use of Laboratory Animals”. </li><li>Working with internal Facilities Operations group to maintain facility, equipment and troubleshoot equipment malfunctions and alarms. </li><li>Monitor and maintain rack washers, robotic cage washing systems, bulk autoclaves, tabletop autoclaves, dump stations, water flush systems, chemical dispensing systems and other associated operational equipment.</li><li>Adherence to internal EHS guidelines and ability to readjust operations as guidelines evolve. </li><li>Order, receive and maintain inventory of supplies such as bedding, chemicals, PPE, caging, caging components, feed and enrichment.</li><li>Manage daily workflow of reusable PPE stocking, collection and laundry pickup. </li><li>Coordinate equipment repairs, including coordination with vendors. </li><li>Maintain areas as “inspection ready” at all times.</li><li>Operate under and enforces strict adherence to safety protocols, biosecurity measures, proper use of PPE and institutional SOPs to ensure safe a working environment at all times.</li><li>Maintain support areas such as, feed rooms, necropsy rooms, animal receiving rooms, chemical storage and supply storage rooms.</li></ul><p><strong>This Job Might Be for You If You: </strong></p><ul><li>Have an interest in science and enjoy hands-on work.</li><li>Thrive in a team environment, can collaborate effectively, and work independently when needed. </li><li>Have excellent verbal, written, time management, organizational and communication skills. </li><li>Have a strong attention to detail and can follow procedures accurately. </li><li>Are comfortable asking questions, providing feedback, and taking initiative. </li></ul><p>A High School Diploma or equivalent technical certification is required. Two or more years of experience operating in a lead role in a cage wash environment. AALAS certification at the ALAT level, or equivalent years of working experience. Strong understand of sanitation procedures and the use of traditional cleaning chemicals typically used in a cage wash setting. Strong leadership, communication and problem-solving abilities. Basic ability to use Outlook, email, PowerPoint, Excel, Microsoft Word, and internal IT applications. The ability to stand for long periods of time, perform repetitive motions, work around chemicals and operate in an environment that may get wet, have elevated temperature and mechanical noise. Perform physical duties such as breaking down pallets, disassembling caging and equipment, processing bulk supplies and moving large drums of chemicals. Operation of a forklift, electric pallet jack, bulk bedding hoist and other associated equipment necessary to maintain operations.</p><p><strong>Work Environment: </strong></p><p>This position involves physical demands, including but not limited to:</p><ul><li>Lifting up to 50 lbs., bending, pushing, pulling, and moving supplies and equipment.</li><li>Extended periods of walking and standing.</li><li>Use of Personal Protective Equipment (PPE).</li><li>Working in environments with potential noise, increased temperature, wet surfaces and allergens.</li></ul><p>Reasonable accommodations will be made for individuals with disabilities to perform essential job functions.</p><p><strong>Weekend and Holiday Requirements:</strong></p><p>This role is classified as essential personnel, meaning weekend and holiday work may be required.</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>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, ERP Product Management (Cloud Fusion)]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45912]]></requisitionid>
    <referencenumber><![CDATA[R45912]]></referencenumber>
    <apijobid><![CDATA[r45912]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45912/senior-director-erp-product-management-cloud-fusion/]]></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 Director, ERP Product Management, leads the strategy, architecture, and delivery of Regeneron’s enterprise ERP capabilities and the broader Finance, Procurement, Tax, Treasury, Accounting, and Supply Chain ecosystem. Working with BRMs, IT leaders, and functional business executives, this leader shapes a cross‑functional, capabilities‑based roadmap aligned to medium‑ and long‑term business goals. The Sr. Director oversees cross‑functionally aligned product managers and partners with program leadership to ensure seamless delivery during the Oracle EBS → Oracle Fusion transition and beyond.</p><p><em><strong>The role will be based onsite at our office in Sleepy Hollow, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Shape the cross‑functional ERP technology strategy with BRMs, IT leaders, and functional executives, building a cohesive, capabilities‑based framework aligned to 3–5+ year business goals.</p></li><li><p>Lead teams of cross‑functionally aligned product managers overseeing solution design, architecture, and delivery in line with product strategy, standards, and enterprise architecture.</p></li><li><p>Align product delivery and technology plans to strategic goals and multi‑function roadmaps; ensure product managers supporting each function meet their strategic objectives.</p></li><li><p>Manage prioritization and alignment using industry standards, best practices, and ERP/cloud trends; regularly update the ERP roadmap to reflect market and business changes.</p></li><li><p>Advise senior leaders on the optimal mix of ERP capabilities and products that balance functional outcomes and technology strategy over a multi‑year horizon.</p></li><li><p>Own the ERP product organization budget; coordinate with product managers and portfolio management to manage demand, forecasting, and the project portfolio; drive strategic product decisions in line with business objectives and budgets.</p></li><li><p>Serve as executive IT owner for Oracle EBS and adjacent platforms; partner across Finance, Procurement, Tax, Treasury, Accounting, HR, Legal, and Supply Chain to deliver capabilities that support enterprise objectives.</p></li><li><p>Partner closely with the Senior Director, ERP Program Management IT Lead (Oracle Fusion) to stay informed of Fusion program milestones, upcoming go-lives, and wave planning — ensuring the operational ERP team is ready to receive and support each new Fusion capability as it is delivered.</p></li><li><p>Drive execution and optimization: configuration, extensions, integrations, data migration, reporting enablement, identity & access governance (RBAC/ABAC), testing (UAT/SIT), deployment, and hypercare.</p></li><li><p>Own the ERP enhancement backlog: triage requests, determine EBS vs. native Fusion design, and prevent capability gaps during the transition and cutover waves.</p></li><li><p>Manage the EBS-to-Fusion cutover period from an operations perspective: maintain EBS stability during parallel run periods, coordinate data freeze windows with business partners, and ensure hyper care support is in place post-go-live.</p></li></ul><p><strong>This role might be for you if have:</strong></p><ul><li><p>Proven success leading global, multi‑entity ERP implementations, upgrades, or modernization programs (EBS → Fusion experience strongly preferred).</p></li><li><p>Deep knowledge of finance and adjacent business processes (Order to Cash, Procure to Pay, Record to Report, Acquire to Retire), and experience with EPM/reporting.</p></li><li><p>Expertise in ERP architecture, integrations (APIs, middleware), data migration, security, identity/access management, and cloud operations.</p></li><li><p>Demonstrated experience establishing governance, change control, and audit readiness (SOX, ITGC; GxP as applicable).</p></li><li><p>Strong portfolio, budget, and vendor/SI management; able to align investment decisions to multi‑year product and technology strategy.</p></li><li><p>Track record of developing product managers and cross‑functional teams; excellent executive communication and stakeholder influence.</p></li></ul><p><br><strong>To be considered for this role, we require:</strong></p><ul><li><p>15+ years of progressive leadership across ERP and enterprise applications, including significant experience with Oracle Fusion Cloud ERP and Oracle EBS.</p></li><li><p>Experience managing ERP operations during parallel EBS and Fusion waves, including cutover planning and hypercare.</p></li><li><p>Hands‑on familiarity with Oracle Tax (EBTax), Treasury (Cash Management/bank connectivity), and/or EPM (planning/forecasting).</p></li><li><p>Background in global ERP rollouts, M&A integrations, and multi‑entity consolidation on Oracle platforms.</p></li><li><p>Oracle Cloud/EBS certifications; MBA or advanced degree.</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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 21:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Strategic Business Planning & Execution]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45148]]></requisitionid>
    <referencenumber><![CDATA[R45148]]></referencenumber>
    <apijobid><![CDATA[r45148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45148/senior-manager-strategic-business-planning-execution/]]></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>As a Senior Manager, Strategic Business Planning and Execution will provide project management support to the Global Medical Affairs (GMA) Head and Medical Directors within the General Medicine Franchise. This role focuses on strategic and tactical planning, budget management, process optimization, and cross-functional collaboration to ensure seamless execution of medical affairs initiatives.<br>The position supports driving operational excellence, implementing digital and workflow tools, and facilitating the alignment of internal functions, external agencies, and alliance partners.</p><p>This position will require you to be on-site 4 days/week at our Sleepy Hollow, NY or Warren, NJ offices. If based in Warren, there will be regular travel to Sleepy Hollow. </p><p><strong>A typical day may include the following: </strong><br>• Partner with Franchise Head, SBP&E Lead, and cross-functional teams to develop and execute Medical Impact Plans (MIPs).<br>• Support the development and monitoring of departmental goals, metrics and achievements to ensure alignment with organizational objectives and drive accountability within the team<br>• Oversee budget preparation, forecasting, accruals, and financial tracking in collaboration with Finance.<br>• Lead end-to-end logistics for multiple assets, including timeline management, resource allocation, and achievement tracking.<br>• Facilitate Medical Impact Team (MIT) meetings to ensure alignment across cross functional collaborators and drive the timely execution of deliverables. <br>• Enhance digital tools, including project tracking systems and dashboards, to enable real-time activity and tracking.<br>• Lead the migration and launch of a SharePoint site, ensuring seamless usability and partner training.<br>• Research and implement IT-enabled workflows to improve operational efficiency (e.g., meeting notes management, finance tracking, procurement systems).<br>• Identify gaps in team capabilities and skills, and collaborate on planning targeted training programs and engaging team-building activities to foster growth and improve performance<br>• Ensure compliant execution of all medical affairs activities in alignment with company SOPs and all relevant industry regulations and guidelines, while ensuring the team has access to relevant and up-to-date SOPs.<br>• Assist in the development and review of procedural documents to meet agency regulations.</p><p><strong>This may be for you if you:</strong><br>• Are skilled in cross-functional teamwork and matrixed project management to align efforts, drive objectives, and ensure compliance.<br>• Have the ability to lead large, cross-functional projects and deliver results on time and within budget.<br>• Want to have an impact on patient lives</p><p>• Thrive on working in a “rapid response" environment. </p><p><br>To be considered, you are to have a Bachelor’s degree with 8+ or master’s degree with 6+ years of experience in healthcare, pharmaceutical, or biotechnology industries. Demonstrated expertise in project management and cross-functional collaboration is required. Proficient in digital tools and workflow automation. Experience with early-phase assets and PMP certification is preferred. Excellent communication, organizational, problem-solving skills, self-motivated and adaptable to a dynamic environment. Experience in strategic planning, budget management, and operational execution. Familiarity with medical affairs activities such as publication plans, advisory boards, and external collaborations. Travel may be required up to 40%</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 12:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro) - Kansas City, MO]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45758]]></requisitionid>
    <referencenumber><![CDATA[R45758]]></referencenumber>
    <apijobid><![CDATA[r45758]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45758/medical-specialist-i-gastro-kansas-city-mo/]]></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[<p><strong>Geography-Kansas City, MO</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><div><p><strong>A Typical Day May Include the Following:</strong></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>This Role May Be for You If:</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>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></ul><p>To be considered you must possess a minimum of a ​Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. 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. Experience with in-servicing and training office staff, nurses and office managers. Ability to partner and collaborate with other internal field teams and alliance partners. Ability to travel and cover large geographic territories.</p></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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Security Specialist]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45967]]></requisitionid>
    <referencenumber><![CDATA[R45967]]></referencenumber>
    <apijobid><![CDATA[r45967]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45967/senior-security-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>We are looking to add a Senior Security Specialist to our growing team. In this role you will monitor, maintain, and improve the physical security systems and protocols of the organization. The role involves tasks such as conducting risk assessments, responding to security incidents, ensuring regulatory compliance, and collaborating with cross-functional teams to implement and enhance security measures.</p><p>As a Senior Security Specialist, a typical day might include the following:</p><ul><li>Assisting in the implementation of new security technologies and processes, including pilot testing, vendor evaluations, and rollout planning.</li><li>Working closely with other departments, including IT and operations, to integrate new security technology and support business continuity</li><li>Assisting with the implementation for standards documentation for security systems, including design basis documents, reference architectures, specifications, as-built drawings, commissioning reports, configuration baselines, and version control.</li><li>Conducting regular security audits and risk assessments to identify vulnerabilities and recommend improvements.</li><li>Ensuring regulatory and compliance alignment relevant to pharma/manufacturing (e.g., GMP expectations in controlled areas, retention and audit trails).</li><li>Supporting crisis management and business resilience programs: contributing to emergency preparedness, incident response workflows, mass notification, muster reporting, and business continuity technology readiness.</li></ul><p>This role might be for you if you:</p><ul><li><p>Can manage multiple concurrent projects, from pilot through rollout and service transition.</p></li><li>Understand cybersecurity principles and have the ability to discuss new technology vulnerabilities and mitigation strategies; can support assessment and risk mitigation process in partnership with cyber IT/OT experts.</li><li>Have proven ability to influence stakeholders and collaborate cross-functionally.</li><li>Can manage procurement cycles and preparing vendor trade-off analyses.</li><li>Have knowledge of OT/ICS and BMS integrations and effective collaboration with IT networking/security teams.</li><li>Possess excellent communication and interpersonal skills, including training delivery and executive-level reporting.</li><li>Are able to work flexible hours, including evenings and weekends, to support implementations and cutovers outside regular business hours.</li></ul><p>To be considered for this position you should have a BA.BS in security management, emergency management, engineering or related field and 5+ years of relevant experience or equivalent combination of education and experience. Ideal candidates will have Certified Protection Professional (CPP), Physical Security Professional (PSP), or similar recognized industry certification. Project management certification (e.g., PMP, PgMP) or equivalent experience is a plus.</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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Trial Optimization]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45082]]></requisitionid>
    <referencenumber><![CDATA[R45082]]></referencenumber>
    <apijobid><![CDATA[r45082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45082/senior-manager-global-trial-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Global Trial Optimization will lead program or study level activities advising on our clinical development strategy, clinical study concepts, study protocols and operational plans that will enable predictable delivery of clinical programs and studies. You will develop and maintain relationships with our external experts facilitating a wide source of country and disease area intelligence used in study design and operational planning. </p><p><strong>A typical day may include the following</strong>: <br>• Lead study level feasibility processes to generate high quality and timely data to inform study design, efficient geographical placement and operational planning.<br>• Partner with teams during CRO led feasibility activities supporting validation of study and country level enrollment rates and study start up timelines to advise budget and baseline setting.<br>• Supports the development and implementation of the Global Trial Optimization function through process initiatives and change management. <br>• Partner with Data and Analytics function to review and identify appropriate central data sources. <br>• Articulate the data story to teams based on country level feasibility and centrally derived data to support data driven decisions to improve protocol design<br>• Project management of study level country landscape assessment activities and the collection of targeted feasibility information for early assessment of operational feasibility for conducting clinical trials.<br>• Lead study level engagements to acquire, analyze and deliver high quality targeted information from external partners. <br>• Prove input into continuous improvement activities to ensure consistency of process execution.<br>• In partnership with Clinical Outsourcing provide functional input into the identification, qualification and relationship management of a range of vendors.<br>• Develop and implement patient recruitment and retention tactics aligned with defined study strategy.<br>• Develop and maintain knowledge of external clinical trial environment and assess developments for impact on study design and execution<br>• May require up to 20% travel</p><p>To be considered a Bachelors degree in a related field with a minimum of 8 years of relevant industry experience within pharma/biotech, a CRO or consulting is required. Strong understanding and experience in operationalizing clinical development programs in a global setting from first-in-human to post-approval. Experience with feasibility. Must be a compelling communicator with ability to translate sophisticated messages to a variety of audiences.</p><p><strong>Additional requirements include: </strong><br>• Experience in using data to inform clinical strategy development<br>• Ability to understand sophisticated business questions and develop effective solutions<br>• Experience in process development, implementation and change management activities<br>• Line management experience preferred<br> </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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro)-Long Beach, Ca]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45901]]></requisitionid>
    <referencenumber><![CDATA[R45901]]></referencenumber>
    <apijobid><![CDATA[r45901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45901/medical-specialist-i-gastro-long-beach-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Long Beach]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Long Beach, CA</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><strong>A Typical Day May Include the Following:</strong></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><strong>This Role May Be for You If:</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>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></ul><p>To be considered you must possess a minimum of a ​Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. 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. Experience with in-servicing and training office staff, nurses and office managers. Ability to partner and collaborate with other internal field teams and alliance partners. Ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Proces Development Engineer III, Bioconjugation Development]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45915]]></requisitionid>
    <referencenumber><![CDATA[R45915]]></referencenumber>
    <apijobid><![CDATA[r45915]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45915/proces-development-engineer-iii-bioconjugation-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>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking and dynamic Process Development Engineer III for its new Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will develop conjugation and purification processes for bioconjugation of proteins to a diverse range of smaller-molecules. You would work in close collaboration with cross-functional teams for process development and optimization using the principles of Quality by Design (QbD) to make the processes suitable for GMP production. This role also involves process scale-up and technology transfer of manufacturing related workflows to Contract Development and Manufacturing Organizations (CDMOs) or Regeneron based manufacturing suites to ensure timely and reliable entrance to the clinic through product commercialization.</p><h3><strong>A Typical Day in the role of Process Development Engineer III might include:</strong></h3><ul><li><p>Working at the bench to design and develop scalable, robust and controlled GMP-ready bioconjugation and purification processes.</p></li><li><p>Collaborating with analytical groups within or outside the organization to establish supportive analytical characterization techniques.</p></li><li><p>Discussing plans and data in cross functional teams to evaluate processes and determine developmental goals and ensure integrated program success.</p></li><li><p>Proactively complying to lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</p></li><li><p>Using statistical design of experiments (DOE) to optimize bioconjugation processes including conjugation reactions, purification operations, and analytical characterization.</p></li><li><p>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to provide technical assessment of CDMO’s intended for GMP production and successfully transferring processes with immediate, first-time success.</p></li><li><p>Researching, identifying, and developing new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT) to ensure robust and controllable bioconjugation and purification processes.</p></li><li><p>Authoring robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</p></li><li><p>Analyzing and presenting data in a clear and cohesive manner to a broad audience facilitating data-driven decision making.</p></li><li><p>Authoring, reviewing, or providing domain expertise for publications, reports, tech transfer documents, regulatory support documents and patents.</p></li><li><p>Being a responsible lab citizen by ensuring timely maintenance of lab equipment, keeping the lab tidy and organized and proactively planning for lab resources.</p></li><li><p>Coaching and mentorship of junior team members of the organization as needed.</p></li></ul><h3><strong>This Role May Be For You If You:</strong></h3><ul><li><p>Enjoy working in the lab to advance exciting new drug modalities to patients.</p></li><li><p>Have strong initiative and aim to complete challenging tasks and learn new technologies.</p></li><li><p>Have a strong fundamental understanding of various protein purification and technology transfer principles</p></li><li><p>Are capable of multi-tasking and working both independently and in a collaborative environment involving cross-functional teams.</p></li><li><p>Have excellent interpersonal, verbal and written communication skills.</p></li><li><p>Can think critically and demonstrate problem-solving skills.</p></li></ul><p>This role requires a Bachelor’s + 10+ years relevant experience or Master’s+ 8+ years relevant experience or a PhD + 0-3 years experience in chemical/biochemical engineering or a related field. Experience with antibodies in the bioconjugates space is highly preferable. Hands on experience with bioconjugation processes (lysine-based, cysteine-based, site-specific etc.) with practical knowledge of downstream purification techniques such as chromatography, ultrafiltration/diafiltration, membrane technologies etc. is preferred. Experience with a variety of analytical characterization tools such as high-performance liquid chromatography (HPLC), UV spectroscopy, etc. is preferred.</p><p>Note: title will be commensurate with experience</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Therapeutic Antibodies]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45095]]></requisitionid>
    <referencenumber><![CDATA[R45095]]></referencenumber>
    <apijobid><![CDATA[r45095]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45095/senior-associate-scientist-therapeutic-antibodies/]]></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><em>Summary: </em></strong></p><p>We are seeking a highly motivated <strong>Senior Associate Scientist</strong> to join our Immunoscreening group in the Therapeutic Antibody team. You will contribute to the identification of potential therapeutic antibodies, the in vitro characterization and selection process of lead molecules in the early antibody drug discovery stage.</p><p><strong><em>Job Duties: </em></strong></p><ul><li>Designing and optimizing in-vitro protein or cell-based immunoassays, including but not limited to flow cytometry, high content imaging, ELISA, AlphaLISA, and MSD, to assess the functional properties of antibody therapeutics with a focus on obesity, muscle metabolism and aging</li><li>Performing medium to high throughput immunoassays according to established protocols</li><li>Compiling and analyzing data by Excel, FlowJo, GraphPad prism and graphic software</li><li>Maintaining mammalian cell cultures for cell-based immunoassays</li><li>Maintaining accurate records of experimental procedures and results</li></ul><p><strong><em>Job Requirements: </em></strong></p><ul><li>Have the ability to multitask and perform data analysis under time pressure</li><li>Can work effectively both independently as well as collaboratively as a team member</li><li>The ability to communicate effectively with your manager as well as within a large team.</li><li>Can be adaptable and flexible with changing priorities</li><li>Have outstanding attention to detail and outstanding organizational skills</li></ul><p>In order to be considered for this role, you must have at least BS/MS degree in cell/molecular biology, immunology, protein biology, or related field with 3-5 years of relevant experience. Knowledge of cell and molecular biology, immunology, or protein biology, skills in aseptic techniques and human and mouse cell culturing, along with hands-on bench research/development experience in in-vitro protein or cell-based assays are preferred. High throughput screening experience, familiarity with liquid handlers and knowledge in obesity/metabolism/aging research are beneficial.</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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 11:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Good Pharmacovigilance Practice Audits (GVP)]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46075]]></requisitionid>
    <referencenumber><![CDATA[R46075]]></referencenumber>
    <apijobid><![CDATA[r46075]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46075/associate-director-good-pharmacovigilance-practice-audits-gvp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>At Regeneron, we are dedicated to transforming lives through innovative medicines and empowering healthcare. We are looking for an outstanding Associate Director, Good Pharmacovigilance Practice (GVP) Audits to join our Global Development Quality Assurance (GDQA) team. This pivotal role offers the opportunity to lead and supervise GVP audits across all aspects of the Regeneron Pharmacovigilance System. As a key member of GDQA, you will play a vital role in ensuring compliance, driving innovation, and mentoring top talent in the field. </p></div><div><p><strong>A Typical Day in This Role:</strong> </p></div><div><ul><li><p>Lead risk-based quality auditing activities, ensuring alignment with international regulations and internal requirements. </p></li></ul></div><div><ul><li><p>Oversee the execution of GVP audits, including scheduling, preparing, conducting, reporting, and follow-up. </p></li></ul></div><div><ul><li><p>Develop and implement new audit standards and methods to stay ahead of technological advancements in global development. </p></li></ul></div><div><ul><li><p>Provide guidance and mentorship to audit teams, encouraging professional growth and excellence. </p></li></ul></div><div><ul><li><p>Manage GDQA resources effectively to meet annual audit schedules and priorities. </p></li></ul></div><div><ul><li><p>Conduct training sessions for GDQA personnel and relevant departments, improving organizational knowledge and skills. </p></li></ul></div><div><p><strong>This Role May Be For You If:</strong> </p></div><div><ul><li><p>You have a deep understanding of EU and FDA Pharmacovigilance regulations, ICH guidance documents, and other relevant compliance standards. </p></li></ul></div><div><ul><li><p>You thrive in dynamic environments and excel at managing multiple high-priority tasks with urgency and precision. </p></li></ul></div><div><ul><li><p>You are a strong leader with experience mentoring teams and interfacing with senior/executive leaders. </p></li></ul></div><div><ul><li><p>You possess exceptional problem-solving skills and can navigate complex situations with critical thinking and strategic insight. </p></li></ul></div><div><p><strong>To Be Considered:</strong> </p></div><div><p>Candidates should possess a bachelor's degree and have at least 11 years of relevant proven experience, including 9+ years of direct GVP auditing and/or industry experience. Strong communication skills and a proven track record in audit and project management are essential. Experience with EU or other regulatory inspections is desirable. Preferred candidates will show talent in stakeholder management, teamwork, critical thinking, and negotiation of complex situations. </p></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 04:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Biostatistics - Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46192]]></requisitionid>
    <referencenumber><![CDATA[R46192]]></referencenumber>
    <apijobid><![CDATA[r46192]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>Regeneron is seeking a Senior Director, Biostatistics to drive our Immunology and Inflammation therapeutic area.</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><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><strong>This role might be for you if have proven experience:</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>To be considered for this opportunity, you must have the following:</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></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>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 16:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Therapeutic Area Genetics (Immunology)]]></title>
    <date><![CDATA[Thu, 26 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46254]]></requisitionid>
    <referencenumber><![CDATA[R46254]]></referencenumber>
    <apijobid><![CDATA[r46254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>We are looking for an extremely talented Scientist to join our Immunology Therapeutic Area Genetics (TAG) team. Within the RGC, 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><p><em><strong>This role will require 4 days per week onsite at our campus in Tarrytown, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong>In this role, a typical day might include the following:</strong></p><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 longitiudinal 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 bacgrounds.</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 job might be for you if you can/have</strong></p><ul><li><p>Bring innovative thinking to human genetics and epidemiological studies</p></li><li><p>Experience leading complex human genetics research incorporating different analytic methods, phenotypes, and study designs.</p></li><li><p>Ability to use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions.</p></li><li><p>Worked with multidisciplinary teams to characterize the functional consequences of discovered disease gene variants</p></li><li><p>Understanding of drug development and clinical trial design and execution. Experience in the clinical management or medical research relating to autoimmune and immune-mediated disease is a plus.</p></li><li></li></ul><p><strong>To be considered for this opportunity, you must have </strong>a PhD , 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. Demonstrated expertise in immunobiology, genetics, and mechanisms; familiarity with large genetic studies that deliver novel genetic findings and medically relevant gene discoveries; and demonstrated ability to manage and collaborate in a multi-disciplinary team, to discover and evolve immunology-related drug discovery pipelines. Individuals with proficiency in computational immunology research are particularly encouraged to apply.</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Mar 2026 19:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist,  CRISPR Screening & Target Identification]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46074]]></requisitionid>
    <referencenumber><![CDATA[R46074]]></referencenumber>
    <apijobid><![CDATA[r46074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46074/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>We are seeking a highly qualified scientist to join the Oncology & Immuno‑Oncology group. The successful candidate will support the identification and validation of novel tumor drug targets using in vitro and in vivo approaches. The ideal applicant is motivated, organized, detail‑oriented, and effective in a fast‑paced, team‑driven environment. Strong communication skills are essential. Experience with murine tumor models, mammalian cell culture, and molecular or cell‑based assays is highly desirable. Familiarity with CRISPR screening is a plus.</p><h3>As a Scientist, CRISPR, a typical day may include:</h3><ul><li><p>Perform vivo tumor experiments in mice, including injection, blood and tissue collection</p></li><li><p>Perform vitro cell culture and molecular biology experiments</p></li><li><p>Analyze and document data, and communicate results clearly and concisely to supervisor and peers</p></li><li><p>Organize and compile results into a finished format for presentation</p></li><li><p>Maintain precise lab notebooks</p></li><li><p>Daily lab maintenance (e.g., ordering reagents and supplies)</p></li></ul><p><strong>To be considered for this role, you must meet the following:</strong></p><ul><li><p>BS or MS with at least 3 years work experience.</p></li><li><p>Experience with mouse tumor models (e.g., subcutaneous implantation, drug dosing, measuring tumors and tumor harvest)</p></li><li><p>Experience with mammalian cell culture</p></li><li><p>Experience with basic molecular biology and biochemistry techniques (e.g., preparation of cell/tissue lysates for DNA/RNA protein analysis, western blots, transfection, PCR, and cloning)</p></li><li><p>Experience designing FACS panels, performing multi-color FACS analysis preferred but not required</p></li><li><p>Experience with CRISPR screens preferred but not required</p></li><li><p>Strong organization and communication skills</p></li><li><p>Strong ability to learn new techniques</p></li><li><p>Ability to work well in a team</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>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Distribution Operations – Japan]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46261]]></requisitionid>
    <referencenumber><![CDATA[R46261]]></referencenumber>
    <apijobid><![CDATA[r46261]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46261/director-distribution-operations-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>We are seeking a dynamic and strategic leader to join our team as the Director of Distribution Operations in Japan. This pivotal role offers the opportunity to shape the distribution network, optimize cost-to-serve, and contribute to delivering best-in-class service in the pharmaceutical sector. If you are passionate about driving operational excellence and fostering collaboration, this is your chance to make a meaningful impact.</p><p><strong>A Typical Day:</strong></p><ul><li>Set the strategic direction and governance model for Japan’s distribution network, including wholesalers and 3PLs.</li><li>Define and manage vendor SLAs/KPIs, conduct quarterly business reviews, and negotiate contracts in collaboration with Legal.</li><li>Oversee distribution budgets, pricing guidance, and rebate programs to support revenue maximization and sustainability.</li><li>Direct implementation and governance of in-market sales data systems, ensuring data quality and delivering actionable analytics.</li><li>Establish standardized processes for claims, returns, and multi-brand Return/Replacement Programs, reducing friction and costs.</li><li>Drive risk management and business continuity planning for distribution operations, including contingency plans and operational risk monitoring.</li><li>Build and lead a high-performing team, fostering a culture of accountability, transparency, and continuous improvement.</li><li>Serve as the senior liaison with wholesalers and key market stakeholders, addressing complaints and supporting sales promotion programs.</li></ul><p><strong>This Role May Be For You:</strong></p><ul><li>You thrive in strategic and analytical roles, translating insights into operational and commercial outcomes.</li><li>You have deep knowledge of GDP, MHLW requirements, trade compliance, contract law basics, and sustainability standards.</li><li>You are skilled in project and program management, capable of handling multiple initiatives, timelines, and stakeholders concurrently.</li><li>You excel in executive communication and negotiation, influencing senior leaders, external partners, and cross-functional teams.</li><li>You are proficient in tools like SAP/S4, WMS/TMS, Power BI/Tableau, SharePoint, and Microsoft Excel/PowerPoint.</li><li>You are passionate about fostering collaboration and developing talent within your team.</li><li>You bring demonstrated success in leading distribution/trade operations in the Japan pharmaceutical market.</li></ul><p><strong>To Be Considered:</strong></p><ul><li>12–15+ years of experience in international biopharmaceutical distribution/trade operations, including cross-functional leadership.</li><li>5+ years of direct people leadership and vendor governance experience.</li><li>Proven expertise in Japan distribution models and wholesaler management; EU/US market exposure is a plus.</li><li>Native level proficiency in Japanese and fluent English; familiarity with Japan-specific cultural business practices.</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 02:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Information]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46258]]></requisitionid>
    <referencenumber><![CDATA[R46258]]></referencenumber>
    <apijobid><![CDATA[r46258]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46258/associate-director-medical-information/]]></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>As Associate Director, Medical Information, you will lead scientific communication and medical information strategy for assigned therapeutic areas, enabling high-quality, compliant scientific exchange with healthcare professionals, patients, and internal team members. You will manage the tactical execution of Global and US Medical Affairs medical information plans, convert insights into strategic recommendations, and serve as a trusted partner. We ensure excellence in delivery while maintaining full adherence to company policies, procedures, and all regulations and industry standards.</p><p><strong>Where & When</strong><br>• On-site 4 days/week in Sleepy Hollow, NY or Warren, NJ<br>• If based in Warren, NJ, occasional travel to Sleepy Hollow, NY is expected<br>• Travel (up to 10% is expected) </p><p><strong>A typical day may include the following: </strong><br>• Develop and deliver high-quality, balanced, and scientifically accurate responses to medical inquiries; resolve complex and brought up inquiries.<br>• Lead the creation and maintenance of deliverables, including literature reviews, Standard Response Documents (SRDs), verbal FAQs, Q&As, AMCP dossiers, and compendium.<br>• Medical reviewer on Promotional and Medical Review Committees, ensuring medical accuracy, clarity, and compliance. <br>• Own department reporting processes and dashboards, including metrics, insights generation, digital analytics, and trend reporting for internal partners.<br>• Evaluate, pilot, and implement AI-enabled tools and technologies to streamline medical information processes and improve efficiency and quality.<br>• Collaborate with global and regional Medical Affairs partners to ensure alignment and share best practices.<br>• Provide scientific support for congress planning, booth activities, and real-time scientific exchange.<br>• Mentor and train new hires and less experienced colleagues; may directly supervise Senior Managers, Specialists, and contractors.</p><p>To be considered a minimum of 5 years of Medical Information experience within the pharmaceutical industry along with a PharmD or PhD is required. Strong scientific knowledge and expertise in a therapeutic area including evaluating and communicating clinical trial and disease state information to a wide range of audiences. Neurology is preferred. Demonstrated experience in conducting scientific literature review, and management of medical inquiries, including the development and review of deliverables (e.g., standard response documents, FAQs, dossier, compendium submissions, etc.). Practical experience and knowledge of FDA guidance’s. <br> </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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 14:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney – Genetics Medicines (CRISPR)]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39465]]></requisitionid>
    <referencenumber><![CDATA[R39465]]></referencenumber>
    <apijobid><![CDATA[r39465]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r39465/director-patent-attorney-genetics-medicines-crispr/]]></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 partner with our research teams in development, protection, and management of the company’s valuable intellectual property in the field of genetic medicines. These genetic medicines are designed to alter genomes and/or gene expression, enabling gene expression, silencing, or editing, and hold promise for treating a variety of diseases and medical conditions. The role will focus on protecting significant therapeutics in clinical development and innovations in genetic medicine technologies, including CRISPR/Cas genome engineering, anti-sense technologies, antibody-targeted therapeutics, and recombineering technologies. </p><p>Key responsibilities for the Patent Attorney include independently collaborating with top-tier scientists and business units to identify inventions relating to genetics medicines therapeutics and/or the technologies that underly such therapeutics, coordinating patent filings and prosecution, and protecting trade secrets. You will handle administrative patent actions, including post-grant oppositions in Europe, and other intellectual property matters, such as due diligence, landscape analyses, freedom-to-operate analyses, and validity assessments. The role also involves advising on emerging legal issues, staying updated on case law and legislative changes, and contributing to projects that uphold the highest legal and ethical standards in the IP Department.</p><p><em><strong>This role will require 4 days per week onsite at our Global HQ Campus in Tarrytown, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong>A typical day may include</strong></p><ul><li>Identify and capture new inventions in CRISPR/Cas genome engineering, anti-sense, antibody-targeted therapeutics, and recombineering technologies.</li><li>Work with outside counsel to prepare and prosecute US and international patent applications.</li><li>Conduct patent landscape, freedom-to-operate, validity, and patentability assessments for Regeneron’s genetic medicines.</li><li>Manage US and foreign administrative patent actions (e.g., post-grant oppositions, third-party submissions, inter partes reviews).</li><li>Assist in litigation activities as needed.</li><li>Support due diligence projects, agreements, transactional work, administrative initiatives, and policy questions.</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>A progressive career collaborating with top-tier scientists and business units to coordinate patent filings, protect trade secrets, and handle administrative patent actions, including post-grant oppositions in Europe.</li><li>Significant expereince advising on emerging legal issues, staying updated on case law and legislative changes, and contributing to projects that uphold the highest legal and ethical standards</li><li>Strong organizational skills and ability to manage multiple projects and competing priorities.</li><li>Ability to handle a large and complex docket with minimal supervision.</li><li>Exceptional communication skills, including presentation, interpersonal, writing, and conflict resolution.</li></ul><p>To be considered for this role you must possess a Ph.D. in life sciences (e.g., molecular biology, genetics, cell biology, immunology, neuroscience) with significant research experience. A Juris Doctorate from an accredited law school and</p><p>admitted to practice before the USPTO and licensed to practice law in at least one state (preferably NY). At least 5 years of experience in biotechnology patent law in a law firm or corporate law department with a minimum 3 years of experience in patent application preparation and prosecution in the biological arts in a law firm setting.</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>$202,000.00 - $336,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, HEOR (HTA, SLR, ITC)]]></title>
    <date><![CDATA[Wed, 30 Jul 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41284]]></requisitionid>
    <referencenumber><![CDATA[R41284]]></referencenumber>
    <apijobid><![CDATA[r41284]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41284/senior-manager-heor-hta-slr-itc/]]></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>As a Senior Manager, HEOR you will contribute to the development of our evidence packages for HTA submissions facilitating product access, reimbursement, and differentiation. Responsibilities involve supporting our evidence synthesis projects (e.g., systematic literature review, meta-analyses, indirect treatment comparisons). We also support cost-effectiveness models, and working closely with our global and regional partners aligning HEOR strategies with market requirements.</p><p>This position is located at our Sleepy Hollow, NY office and is on-site for 4 days/week. We cannot offer a hybrid or fully remote options. If eligible, we can offer relocation benefits.</p><p><strong>A typical day may include the following: </strong><br>• Participate in the development of our observational research studies, cost-effectiveness, and budget impact models, to support reimbursement dossiers.<br>• Collaborate with cross-functional our business partners to develop and support product value propositions that optimize access, reimbursement, and uptake, ensuring alignment with HTA requirements.<br>• Identify HEOR evidence gaps and design studies and tools to demonstrate relative value and product differentiation for submissions.<br>• Develop and implement HEOR strategies to support commercialization activities, including the preparation of HTA submissions and addressing payer requirements.<br>• Evaluate HTA decisions and apply insights to pipeline and marketed products, ensuring submissions meet regulatory and payer expectations for value demonstration and reimbursement.<br>• Report, publish, and present HEOR data and study results, ensuring compliance with regulatory standards and effectively communicating evidence to collaborators. </p><p><strong>This may be for you if you: </strong><br>• Want to have an impact on patient lives<br>• Enjoy working in a ‘rapid response’ environment<br>• Can demonstrate knowledge of HTA, SLR and ITC<br>• Would like an opportunity to present to senior leaders</p><p>To be considered you are to have a Master’s degree in an HEOR related major with a PhD or PharmD being. Your experience needs to include 2+ years of experience in the pharmaceutical industry or in a HEOR consulting organization. Experience required includes the design and conduct of evidence synthesis projects and knowledge of pairwise and network meta-analysis, as well as population-adjusted indirect comparison. Experience in developing and managing HEOR projects that align with the ISPOR guidelines and support HTA regulatory submissions (e.g., NICE) is helpful. Customer-facing experience at country level is required. US managed care experience is a strong advantage. <br> </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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$148,300.00 - $241,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Sciences, Internal Medicine]]></title>
    <date><![CDATA[Sun, 19 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43175]]></requisitionid>
    <referencenumber><![CDATA[R43175]]></referencenumber>
    <apijobid><![CDATA[r43175]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43175/associate-director-clinical-sciences-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>The Associate Director, Clinical Sciences contributes 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. Works 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. Reports 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>As an Associate Director, a typical day may include the following:</p><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><p>This role may be for you:</p><ul><li><p>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><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>You possess strong cross-functional management, interpersonal skills, and strong attention to detail</p></li></ul><p>To be considered for this role, a bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc). ≥ 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Metabolic disease and/or inflammatory disease areas. We are seeking proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills. We need an individual who is a strong team-player. Experience in all aspects of conducting global clinical trials and execution of clinical programs. Other levels considered depending on experience. Experience in managing trials in one or more of the following therapeutic areas - cardiovascular, renal, metabolic and/or inflammatory disease - required. #Obesity</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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$173,500.00 - $283,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Drug Development Program Management]]></title>
    <date><![CDATA[Mon, 24 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43321]]></requisitionid>
    <referencenumber><![CDATA[R43321]]></referencenumber>
    <apijobid><![CDATA[r43321]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43321/director-drug-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>Using extensive program management knowledge and experience in the drug development industry, the <strong>Director, Development Program Management</strong> provides operational leadership, direction and support to a team, program or project of moderate to large scope, [within a given Therapeutic Area] as well as to the DPM department as a whole. The Director, Development Program Management executes the strategic direction of a program from preclinical through commercialization by driving the development and implementation of integrated [project] program plans, goals, budgets, and timelines. Director, Development Program Management is responsible for the successful operation of activities of major significance to the organization. </p><p><strong>In a typical day you will:</strong></p><ul><li>Provide operational leadership, direction and support of a program throughout its lifecycle, by integrating key stakeholders from Discovery, Manufacturing, Preclinical, Global Development and Commercial. </li><li>Independently lead multiple or complex development programs. </li><li>Partner with the Strategic Program Lead to provide operational leadership of program(s) and supports development and execution of overall program strategy by facilitating cross-functional Strategic Development Team. Independently assesses and proactively addresses the needs of the program from pre-IND through commercialization and makes operational decisions to support requirements for success. Strengthens and leads high performance teams. </li><li>Leverage significant project management experience and knowledge of the drug development process, drives team alignment in creation of integrated project / program plans, timelines and budgets. Ensures efficient delivery of plans. Directs annual program goal setting in alignment with Regeneron’s overall goals and monitors progress against these goals. Champions potential program risks and ensures contingency plans are in place. </li><li>Act as a key liaison between Regeneron and our strategic alliance partners and collaborators (where applicable). Prepares, provides input, and / or manages the process involving major presentations for collaboration meetings effecting key business decisions. Responsible for facilitating and driving decision making in support of the joint strategic objectives of the program. </li><li><strong>Communication:</strong> Ensures effective, accurate, and timely scientific / technical program-related communication to the team and Sr. Management. Adept at tailoring communications based on audience, effectively framing and communicating nuanced context for stakeholders and capturing rationale for decisions.</li></ul><p><strong>This role may be for you if you: </strong></p><ul><li>Have excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company in order to establish credibility with professionals on the project teams. </li><li>Understand and motivate others and build effective teams. </li><li>Have strong presentation and critical thinking skills. </li><li>Actively promote constructive interactions among team members in order 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 (both project and self) </li><li>Thrive in fast paced organizations; expert in dealing with ambiguity and uncertainty </li></ul><p><strong>In order to be considered qualified</strong>, you must have a Bachelor's degree and 12+ years of in-house pharmaceutical program management with knowledge of the drug development process as well as understanding of clinical trials.</p><p>#hematology </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>$180,400.00 - $300,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Global Procurement IT]]></title>
    <date><![CDATA[Sun, 14 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44068]]></requisitionid>
    <referencenumber><![CDATA[R44068]]></referencenumber>
    <apijobid><![CDATA[r44068]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44068/executive-director-global-procurement-it/]]></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 Executive Director, Global Procurement – IT, is responsible for shaping and executing a forward-thinking global IT Procurement strategy that aligns with the organization's overarching business objectives and delivers measurable strategic value. This critical leadership role spans IT Services, Software, Hardware, and Telecoms, focusing on optimizing procurement performance across these categories to drive competitive advantage and enterprise-wide efficiency.</p><p>Reporting to the Head of Indirect Procurement, the Executive Director will act as the primary representative of Global Procurement in decisions that shape the organization’s IT procurement landscape, influencing both short- and long-term success. The role requires a visionary leader who can anticipate market trends, foster innovation, and build strategic partnerships to deliver lasting value.</p><p>In addition to driving strategy, the Executive Director will lead and inspire a team of procurement professionals, cultivating a high-performance culture that emphasizes collaboration, innovation, and inclusivity. By providing mentorship and thought leadership, the individual will empower the team to exceed expectations and contribute to the organization’s strategic growth and operational excellence.</p><p><strong>A typical day in this role might look like: </strong></p><ul><li>Collaborate with senior executive leadership within IT and across the organization to identify transformative opportunities and drive innovation, aligning initiatives with strategic objectives to deliver measurable value and competitive advantage</li><li>Lead the development and execution of global IT procurement category strategies, aligning with business and stakeholder priorities.</li><li>Translate category strategies into actionable sourcing projects that deliver measurable value.</li><li>Partner with Indirect Procurement leadership and other stakeholders to ensure strategies evolve with organizational needs and goals.</li><li>Provide expert insight on IT procurement categories, including IT services, software, hardware, and telecoms</li><li>Cultivate and sustain strategic, high-impact relationships with senior executive stakeholders to drive measurable results, influence critical decision-making on make-or-buy operating models, and align procurement initiatives with organizational objectives</li><li>Lead high-impact negotiations and supplier management initiatives. Foster and develop strategic partnerships with key suppliers to drive innovation, value creation, and long-term success.</li><li>Execute a best-in-class vendor management program for IT suppliers and ensure compliance with GxP and applicable regulations.</li><li>Drive process improvements to enhance stakeholder experience and ensure seamless IT service delivery.</li><li>Use data-driven decision-making to deliver successful category projects and optimize procurement processes.</li><li>Ensure compliance with procurement policies, procedures, and regulatory requirements.</li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Bachelor’s degree in a relevant field of study; advanced degree preferred.</li><li>15–20 years of progressive experience in procurement, including substantial experience in IT procurement categories.</li><li>Proven success in leading global categories, teams, processes, and suppliers in a multi-national organization.</li><li>Experience managing senior level professionals and leading cross-functional teams.</li><li>Strong negotiation and contract management skills specific to IT vendors and suppliers.</li><li>Proficiency in sourcing and contracting tools, ERP systems, and eRFx platforms (e.g., Oracle, Zycus, Ariba).</li><li>Ability to leverage standard business applications for communication, presentation, and data analysis (Word, Excel, PowerPoint).</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Summer 2026 MD Intern, Internal Medicine]]></title>
    <date><![CDATA[Wed, 22 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43354]]></requisitionid>
    <referencenumber><![CDATA[R43354]]></referencenumber>
    <apijobid><![CDATA[r43354]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Marketing - Oncology]]></title>
    <date><![CDATA[Sun, 25 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44802]]></requisitionid>
    <referencenumber><![CDATA[R44802]]></referencenumber>
    <apijobid><![CDATA[r44802]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44802/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[<p><strong>SUMMARY/POSITION OBJECTIVE:</strong><br>As a Regeneron Japan’s marketing team, Regeneron needs an experienced Product Manager who will be responsible for leading Regeneron Japan’s local oncology marketing activities.<br>Reporting to Sr Marketing Manager in Japan, he/she will be accountable for brand marketing activities in Japan for both currently commercialised indications and any future launches, working closely with cross-functional and cross-regional stakeholders to ensure seamless execution of the country strategic and tatical brand plan.</p><p><strong>JOB DUTIES:</strong><br>• Accountable for overarching brand marketing strategy in Japan and provides input into the development of the global brand strategy, functional plans and budget. <br>• Lead the local brand planning process including analyzing the competitive landscape, identifying key promotional opportunities, developing customer-focused and differentiated messages to key target audiences.<br>• As part of the local brand planning process, work in partnership with local counterparts in Medical Affairs to create and agree on an aligned brand strategy.<br>• Collaborate with cross-functional teams to implement promotional activities defined in the brand plan. <br>• Analyse drivers and barriers of brand performance (e.g. share of voice, market dynamics, competitive actions) and identify/propose actions to address opportunities or risks to performance. <br>• Responsible for the development and execution of external stakeholder engagement plans (including national congresses, HCP meetings etc) in coordination with cross-functional teams.<br>• Creation of local promotional materials aligned with the local and global brand plans for use by the sales force and via digital channels.<br>• Working closely with the Sales Team in the development and execution of the Field Plan of Action, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/stakeholders.<br>• Develop local promotional budget and manage spend in line with approved budget.<br>• Maintain the highest ethical and compliance standards.</p><p><strong>REQUIREMENTS:</strong><br>Required<br>• Bachelor's degree required with preference for science background; <br>• 5+ years of biotech/pharma brand marketing experience <br>• Expertise in managing ad agency and suppliers, developing annual budgets. <br>• Strong integrity and ethics in behaviors, actions, and communications.<br>• Ability to communicate and act promptly, demonstrated initiative, creativity, and ability to work effectively in complex, rapidly changing environments. Excellent planning, prioritization, communication and presentation skills<br>• Ability and willingness to travel as required 30-40%, some on weekends for conferences and meetings<br>• Working knowledge of local healthcare compliance codes and any regulations related to promotional activities.<br>• Written and spoken English language skills. <br>• +7 years relevant experiences</p><p>Preferred<br>• Experience preferred in oncology marketing.<br>• Launch experience a plus.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 26 Jan 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement-Direct]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44723]]></requisitionid>
    <referencenumber><![CDATA[R44723]]></referencenumber>
    <apijobid><![CDATA[r44723]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>We are currently looking to fill a Director Global Procurement, Direct position within our team. In this role you will develop a holistic Category Strategy and provide strategic leadership and direction with a focus on CMO & External Manufacturing Procurement. The position focuses on a very exciting part of Regeneron’s molecule portfolio which includes Drug Product & Drug Substance for Mab’s, Advanced Therapies and other therapeutic areas. This role will be critical to driving performance across the IOPS External Manufacturing categories including alignment with stakeholder goals, driving towards competitive advantages (strategic and financial) and optimizing supplier relationships. This role works in close collaboration with IOPS Stakeholders to enable company revenue targets and the new product pipeline.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Lead the composition, development and execution of category strategies in CMO External Manufacturing, Drug Substance & Drug Product.</p></li><li><p>Translate category strategies into achievable and meaningful sourcing projects that deliver value to Regeneron and its patients.</p></li><li><p>Partner with Direct Procurement Leadership colleagues to ensure strategies evolve as Regeneron and its pipeline evolves.</p></li><li><p>Implement category strategies to meet objectives.</p></li><li><p>Collaborate with other parts of Global Procurement to best manage cross-category suppliers.</p></li><li><p>Anticipate needs and plan strategies to optimize achievement of corporate goals.</p></li><li><p>Collaborate and execute a best-in-class partner management program.</p></li><li><p>Implement and manage technology solutions to drive value via efficiency and effectiveness.</p></li><li><p>Build and manage a team that provides all CMO Procurement support globally.</p></li><li><p>Continually enhance capability and capacity through ongoing talent development establishing/communicating criteria for evaluating staff performance; managing direct reports, implementation of consistent work processes; and drive process excellence with a focus on stakeholder experience</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Believe that value can be driven through strategic partnerships and efficient ways of working.</p></li><li><p>Can tap into strong in-depth knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of a Global Procurement organization.</p></li><li><p>Enjoy successfully leading global categories or global teams, processes, and suppliers within a multi-national organization.</p></li><li><p>Serve as role-model leader consistently exhibiting behaviors across an organization of direct reports to create clarity, provide a clear and understandable vision with transparency and trust both within and outside of the organization.</p></li><li><p>Can demonstrate success leading cross-functional teams to drive results in CMO, External Manufacturing categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Can influence and partner with senior executives and peer functions to drive strategic change and efficiency.</p></li><li><p>Have working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Have experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><ul><li><p>Director: 12+ years of experience in relevant functions or industries. The ideal candidate will have in-depth knowledge of CMO’s & External Manufacturing, Raw Materials or Packaging Technologies in the Pharmaceutical field procurement categories.</p></li></ul><p>This role requires working onsite 5 days per week.</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>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Thu, 15 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44633]]></requisitionid>
    <referencenumber><![CDATA[R44633]]></referencenumber>
    <apijobid><![CDATA[r44633]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44633/director-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>The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities will include support to some clinical study activities. The candidate will also supply, lead and/or supervise IND/CTA and BLA submissions activities.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide interpretation of regulatory authorities’ feedback, policies and guidelines.</p></li><li><p>Lead the development of regulatory strategic plans either directly in conjunction with project teams or through your reports. Own the preparation of major clinical submissions required for regulatory approval.</p></li><li><p>Work with project teams to resolve complex project issues. Utilize regulatory expertise and knowledge of regulatory requirements and regulations to strategically interpret, plan, and communicate requirements to ensure attainment of governmental approvals.</p></li><li><p>Responsible for quality and timeliness of IND/CTA and BLA submissions. Interact with other functions and partners, in the preparation, review, and completion of documents for regulatory submissions.</p></li><li><p>Successfully plan, prioritize, supervise and/or conduct activities in close collaboration with leads from other areas. Assure compliance with regulations and with project team timelines.</p></li><li><p>Provide interpersonal support and lead personnel.</p></li><li><p>Critical thinking, leadership skills, assertiveness, excellent negotiation and project management skills as evidenced by past performance on drug development project teams</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>If you bring strong 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><p><strong>To be considered,</strong> you must possess excellent written and verbal communication skills along with a MD, Ph.D. or Pharm D. degree. We expect a minimum of 10 years of pharmaceutical industry experience, at least 7 of which should include regulatory experience.</p><p><em>This role requires you to work onsite 4 days per week in either Warren, NJ, Tarrytown, NY or Cambridge, MA. If you are not local and qualify we can offer relocation support. </em></p><p>#MDJOBSRA #GDRAJobs</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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 16 Jan 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Strategic Customer Engagement, Neurology CBU]]></title>
    <date><![CDATA[Thu, 29 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44930]]></requisitionid>
    <referencenumber><![CDATA[R44930]]></referencenumber>
    <apijobid><![CDATA[r44930]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44930/executive-director-strategic-customer-engagement-neurology-cbu/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Executive Director, Strategic Customer Engagement, Neurology CBU (Commercial Business Unit) is a leadership role within Neurology Commercial Business Unit of Regeneron. The incumbent will report to the Vice President heading the CBU and will be based in the corporate headquarters in Sleepy Hollow, NY.</p><p>The primary expectations for this role are two-fold:</p><p>1) Provide strategic oversight and enhance launch and execution excellence for our newly launching brand for Myasthenia Gravis in the US; 2) Create a strategic coordinated approach for our field teams calling on customers. The incumbent will be responsible for optimizing business performance for the Neurology Sales Specialists. They will lead the Field teams, motivating and developing the team to deliver upon CBU operational and financial goals and customer expectations.</p><p>Specifically, the individual will have accountability for providing strategic leadership and cross-functional direction to successfully drive the launch for Regeneron’s neurology brands – beginning with Myasthenia Gravis and expanding over time with our robust Neurology pipeline, navigating all relevant cross functional teams to successfully deliver Regeneron’s neurology portfolio to patients in need.</p><p>The individual must be capable of developing credible and trusted relationships with all Field teams as well as aligning, through knowledge and experience, colleagues in Marketing, Market Access, Field reimbursement, Commercial Operations, Trade and Distribution and Medical Affairs. They must also align collaboration with key collaborators across the rest of the Commercial, Corporate and R&D organizations.</p><p>The Executive Director, Strategic Customer Engagement must foster a customer/patient driven Regeneron culture ensuring patients are first in all business activities. This must be accomplished while continuing to deliver Field commitments within budget, revenue targets and timelines while remaining steadfast in ensuring Field team compliance with federal, state and local laws, industry regulations and guidelines.</p><p><strong>In this position a typical day may include the following:</strong></p><ul><li>In collaboration with the VP, Head of CBU, develop and implement a commercial customer-facing strategy that will enable Regeneron to become a major player serving the Neurology market.</li><li>Contribute to the development of the Company’s strategic commercial plan to significantly and profitably grow the business.</li><li>Provide field leadership and direction to the Neurology customer-facing field teams including hiring, motivating, and developing the team to deliver upon customer expectations.</li><li>Establish credible and trusted relationships with key organizational and business collaborators inside and outside of Regeneron including key health care providers, Key opinion leaders, etc.</li><li>Establish individual business relationships and a strong presence with experts in the field and be able to develop key relationships with experts in the Neurology therapeutic area.</li><li>The individual must be capable of developing credible and trusted relationships with direct reporting personnel in the Field, as well as aligning through knowledge and experience, colleagues in Marketing, Market Access, Field reimbursement, Commercial Operations, Trade and Distribution and Medical Affairs. They must also align collaboration with key partners across the rest of the Commercial organization, Corporate and R&D organizations.</li><li>Lead a high quality, high performing field team capable of realizing fully Regeneron’s technology and commercial promise to patients. This must be accomplished while continuing to deliver Field commitments within budget, revenue targets and timelines.</li><li>Ensure Regeneron Executive Leadership is kept aware of significant external events and threats that may affect our business and proactively make recommendations to address them in a timely manner.</li><li>Ensure Field team compliance with federal, state and local laws, industry regulations and guidelines at all times.</li></ul><p><strong>This May Be the Right Role for You If you:</strong></p><ul><li>You are a seasoned commercial executive and proven leader with sophisticated management skills and a solid track record of accomplishment. Experience in both major pharmaceutical and in biotech companies is preferred with a recent track record of successful product launches in the injectable biologics therapeutic area. Neurology experience is preferred and Myasthenia Gravis or Neurology Rare Disease experience a plus.</li><li>You have experience in leading highly successful field teams.</li><li>You demonstrate strategic and tactical abilities in developing and successfully implementing a comprehensive sales plan. This must be accomplished while continuing to deliver Field commitments within budget, revenue targets and timelines.</li><li>You are capable of establishing governance to ensure the Neurology CBU remains at all times aligned with federal, state and local laws, industry regulations and guidelines ensuring Field team compliance with federal, state and local laws, industry regulations and guidelines.</li><li>You can quickly display credibility and build support for necessary initiatives within the CBU and across other related functions and Regeneron.</li><li>You are an analytical decision maker with the proven ability to complete and deliver on business objectives.</li><li>You bring high energy, inspirational leadership skills with exceptional communication and team building ability.</li></ul><h3>To be considered for this role you bring,</h3><ul><li>BS in a life sciences or related field; MBA preferred.</li><li>Recent launch experience in the Rare Neurology injectable market a strong plus.</li><li>Minimum of 15 years people and industry leadership experience through progressively increasing leadership positions.</li><li>Strong leadership skills required including strong record of hiring, developing and retaining personnel while delivering agreed revenue targets.</li><li>Experience in biologic products and experience in the “buy and bill” reimbursement area is required.</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 30 Jan 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44660]]></requisitionid>
    <referencenumber><![CDATA[R44660]]></referencenumber>
    <apijobid><![CDATA[r44660]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44660/senior-manager-internal-medicine-clinical-scientist-immuneinflammatory/]]></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>The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p></div><div><div><div><div><p><strong>As a Senior Manager in Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Develops/maintains 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>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Collaborates with internal functions and external vendors to promote clinical study integrity</p></li><li><p>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>Demonstrated ability to influence within team and may influence cross functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in one or more of the following therapeutic areas – Immune/Inflammatory related clinical trials.</p></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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I -Dermatology- Morristown, NJ]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45006]]></requisitionid>
    <referencenumber><![CDATA[R45006]]></referencenumber>
    <apijobid><![CDATA[r45006]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45006/medical-specialist-i-dermatology-morristown-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>Geography: Morristown, New Jersey (Hoboken/Jersey City/Piscataway/ Newark)</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Feb 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product Specialist Dermatology (Campania Nord)]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45298]]></requisitionid>
    <referencenumber><![CDATA[R45298]]></referencenumber>
    <apijobid><![CDATA[r45298]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45298/product-specialist-dermatology-campania-nord/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea meets the right team, meaningful change can happen. By working within our growing network to invent, develop, and bring to patients therapies that can transform the lives of people with serious diseases, we are creating new ways of thinking about science, manufacturing, commercialisation - and health.</p><p>Join our new Immunology Sales team in Italy. As a Sales Specialist, you will contribute to achieving Immunology sales targets, always keeping Regeneron’s commitment to patient care at the centre. We are looking for people with a hands-on approach, strong commercial judgement, the ability to manage priorities and resources, and a proven track record of results (meeting or exceeding targets). The ideal candidate thinks critically, organises time effectively, and manages stakeholder engagement in a focused way, bringing value and targeted solutions.</p><p><strong>Job duties</strong></p><ul><li><p>Deliver key brand messages in the territory, aligned with the agreed strategy.</p></li><li><p>Contribute to the development of the territory tactical plan by providing market and local territory insights, in line with the product brand plan.</p></li><li><p>Use available market data to define the action plan for your territory.</p></li><li><p>Manage required administrative activities (expense notes, marketing/field insight reports, call reporting).</p></li><li><p>Operate in compliance with Regeneron regulatory, legal, and compliance guidelines.</p></li><li><p>Participate in local, regional, and national meetings as required.</p></li><li><p>Work collaboratively with alliance partners, contributing to shared objectives.</p></li></ul><p><strong>Requirements</strong></p><ul><li><p>Excellent relationship-building and customer engagement skills, with a value-based focus.</p></li><li><p>Strong scientific and technical knowledge, with the ability to deliver disease and concept selling activities.</p></li><li><p>Strong written, verbal, and presentation communication skills.</p></li><li><p>Strong planning and organisational skills.</p></li><li><p>Ability to present ideas clearly to individuals or groups, adapting the message to the audience.</p></li><li><p>Ability to work independently and contribute to the development of territory tactical plans.</p></li><li><p>Good working knowledge of Microsoft Office (Word, Excel, PowerPoint) and email/CRM tools.</p></li><li><p>Degree (or equivalent qualification) and 5 years’ experience as a pharmaceutical representative (or equivalent role), with hospital-level activity.</p></li><li><p>Experience in the biologics market is a plus.</p></li><li><p>Experience in Dermatology and/or experience working with or engaging hospital paediatricians 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 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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Product Specialist Dermatology (Lombardia Est)]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45295]]></requisitionid>
    <referencenumber><![CDATA[R45295]]></referencenumber>
    <apijobid><![CDATA[r45295]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45295/product-specialist-dermatology-lombardia-est/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea meets the right team, meaningful change can happen. By working within our growing network to invent, develop, and bring to patients therapies that can transform the lives of people with serious diseases, we are creating new ways of thinking about science, manufacturing, commercialisation - and health.</p><p>Join our new Immunology Sales team in Italy. As a Sales Specialist, you will contribute to achieving Immunology sales targets, always keeping Regeneron’s commitment to patient care at the centre. We are looking for people with a hands-on approach, strong commercial judgement, the ability to manage priorities and resources, and a proven track record of results (meeting or exceeding targets). The ideal candidate thinks critically, organises time effectively, and manages stakeholder engagement in a focused way, bringing value and targeted solutions.</p><p><strong>Job duties</strong></p><ul><li>Deliver key brand messages in the territory, aligned with the agreed strategy.</li><li>Contribute to the development of the territory tactical plan by providing market and local territory insights, in line with the product brand plan.</li><li>Use available market data to define the action plan for your territory.</li><li>Manage required administrative activities (expense notes, marketing/field insight reports, call reporting).</li><li>Operate in compliance with Regeneron regulatory, legal, and compliance guidelines.</li><li>Participate in local, regional, and national meetings as required.</li><li>Work collaboratively with alliance partners, contributing to shared objectives.</li></ul><p><strong>Requirements</strong></p><ul><li>Excellent relationship-building and customer engagement skills, with a value-based focus.</li><li>Strong scientific and technical knowledge, with the ability to deliver disease and concept selling activities.</li><li>Strong written, verbal, and presentation communication skills.</li><li>Strong planning and organisational skills.</li><li>Ability to present ideas clearly to individuals or groups, adapting the message to the audience.</li><li>Ability to work independently and contribute to the development of territory tactical plans.</li><li>Good working knowledge of Microsoft Office (Word, Excel, PowerPoint) and email/CRM tools.</li><li>Degree (or equivalent qualification) and 5 years’ experience as a pharmaceutical representative (or equivalent role), with hospital-level activity.</li><li>Experience in the biologics market is a plus.</li><li>Experience in Dermatology and/or experience working with or engaging hospital paediatricians is a plus.</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 04:26:41 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, CMC Regulatory Affairs (Obesity)]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45184]]></requisitionid>
    <referencenumber><![CDATA[R45184]]></referencenumber>
    <apijobid><![CDATA[r45184]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45184/associate-director-cmc-regulatory-affairs-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>As an Associate Director you will lead the development and execution of global CMC regulatory strategies for our Obesity portfolio. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.</p><p>This position is onsite 4 days/week at either our Tarrytown or Rensselaer, NY or Warren, NJ offices. We cannot offer a a remote work option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Lead product development activities from a CMC regulatory standpoint with input from senior management.<br>• Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post-approval activities.<br>• Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work-arounds, and obtain consensus. <br>• Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.<br>• Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).<br>• Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents; <br>• Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.<br>• Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.<br>• Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.<br>• Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.<br>• Find opportunities to initiate operational changes and policy modifications.<br>• Manage and coach team member(s). </p><p>This may be for you if you: <br>• Have a strong grasp of CMC worldwide regulations and guidelines.<br>• Have been successful in building collaboration and teamwork across cross-functional teams.<br>• Proven track record managing and mentoring people.<br>• Demonstrated skill in managing multiple priorities.</p><p>To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred. Proven track record supporting small molecule drugs and/or biological products through development and approval is a distinct advantage. It is required to have a good understanding of current CMC worldwide regulations and guidelines. Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.<br> </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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Global Program Head - Oncology]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45150]]></requisitionid>
    <referencenumber><![CDATA[R45150]]></referencenumber>
    <apijobid><![CDATA[r45150]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45150/vice-president-global-program-head-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 Global Program Head (GPH) for Oncology leads integrated strategy and execution for one or more REGN oncology antibody programs from lead selection through Biologics License Application (BLA). The GPH co-leads the asset strategic team with a clinical co-leader, aligns cross-functional stakeholders, and ensures Executive Management has the right information to authorize program strategy decisions. This role spans discovery through late-stage development and interfaces broadly across research, development, and commercial functions to deliver high-quality, scientifically rigorous, and competitive development plans.</p><h3><strong>Key Responsibilities</strong></h3><ul><li>Drive creation and continuous refinement of an integrated, end-to-end program strategy from discovery through late-stage development and BLA submission</li><li>Co-lead the asset strategic team with the clinical co-leader; provide program oversight, execution discipline, and risk/issue management</li><li>Identify, engage, and align key stakeholders across REGN and partners to ensure input and accountability for program strategies and plans</li><li>Provide strategic guidance across research, nonclinical, clinical, medical safety, CMC/supply (toxicology, clinical and commercial materials), regulatory, and commercial needs</li><li>Ensure scientific rigor and innovation are embedded in program decision-making and development plans</li><li>Integrate cross-functional perspectives on scientific rationale, operational feasibility, budget, timeline, and competitive/commercial landscape</li><li>Translate strategy, recommendations, and trade-offs clearly between teams and senior leadership; prepare and deliver high-quality discussions and presentations to facilitate decisions</li><li>Represent Regeneron at joint development committees as needed and maintain productive external partner interactions</li></ul><h3><strong>Qualifications</strong></h3><ul><li>MD, PhD, or PharmD required</li><li>15+ years of broad oncology drug development experience, with substantial expertise in oncology clinical development</li><li>Proven track record advancing programs through key development milestones and/or approval in biotech/pharma; biologics experience strongly preferred</li><li>Deep knowledge of the competitive landscape and regulatory pathways for oncology drug approval</li><li>Demonstrated ability to build and lead high-performing, cross-functional teams in a highly matrixed environment without direct line authority</li><li>Strong strategic thinking, stakeholder management, and communication skills; adept at influencing across functions and levels</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>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Medical Operations, Externally Sponsored Research Collaborations]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45123]]></requisitionid>
    <referencenumber><![CDATA[R45123]]></referencenumber>
    <apijobid><![CDATA[r45123]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45123/director-medical-operations-externally-sponsored-research-collaborations/]]></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><div><p>The Director, Medical Operations, will manage our Externally Sponsored Research (ESR) Collaboration program. Responsibilities will also include people management, maintaining appropriate structure and procedures to support our growth. Additionally, you will ensure timely deliverables and financial management support. <br>This position is at our Sleepy Hollow, NY office and will require you to be on-site 4 days/week. We cannot offer a remote work option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Support of Investigational and/or Commercialized Products, including non-filing post-marketing research activities, timelines, results, budgets, forecasting, disclosures, and compliance. <br>• Support of Late-Stage Molecules and launch readiness activities. <br>• Support of Early Phases molecules, post-IND filing, ensure non-clinical and non-drug studies are reviewed in line with our strategy. <br>• Develop a team ensuring growth-minded goals, and development plans. <br>• Ensuring efficient alignment with both Alliance and internal partners. <br>• Ensure External Sponsored Research (ESR) programs are led compliantly. <br>• Program planning, allocation and movement of program budgets, timelines and program results, risk strategy/mitigation planning, and ensuring annual review of Areas of Interest. <br>• Supervise all budgeting aspects including annual planning, initial projections for upcoming activities/programs, drug related costs, reforecasts, actuals, and accrual information. <br>• Coordinate appropriate drug/material planning including timing of drug and labeling campaigns, expiry events and potential impact, and ensuring compliance for shipments, temp excursions, and quarantines. <br>• Compliance: ESR Processes, FMV, Safety, Regulatory, Training. <br>• Adheres to and ensures team adherence to all applicable SOPs, working guidance, workflows, required reporting, and maintaining support of programs. Create/update relevant SOPs, working practices, forms and tracking documents as needed, ensuring audit readiness </p><p><strong>This may be for you if you:</strong> <br>• Support medical focused Externally Sponsored Research, Investigator Initiated Studies and/or Research Collaborations. <br>• Want to have an impact on patient lives <br>• Can demonstrate a track record of being successful in fast-paced, dynamic environment. <br>• Enjoy influencing management both internally and externally. </p><p>To be considered, a bachelor’s degree is required along with 11+ years active work experience in area of clinical research, regulatory or field-based function in the pharmaceutical industry. Experience in Medical Study Operations is required. Experience leading a team of 2+ ensuring goals are achieved. Ability to redirect and create solutions for new regulations or anticipation of updated regulations. A science background ideally in the therapeutic areas of oncology is preferred<br> </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 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[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Columbus, OH]]></title>
    <date><![CDATA[Tue, 24 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45635]]></requisitionid>
    <referencenumber><![CDATA[R45635]]></referencenumber>
    <apijobid><![CDATA[r45635]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45635/medical-specialist-i-dermatology-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>Geography: Columbus, OH</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$154,300.00 - $196,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Feb 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (f/m/d) - Bremen - Osnabrück - Oldenburg]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45946]]></requisitionid>
    <referencenumber><![CDATA[R45946]]></referencenumber>
    <apijobid><![CDATA[r45946]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45946/sales-specialist-oncology-fmd-bremen-osnabrueck-oldenburg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Für unser Field Sales Team in der Onkologie suchen wir Sie als</p><p><strong>Sales Specialist Onkologie (w/m/d)</strong></p><p>im Gebiet: <strong>Bremen - Osnabrück - Oldenburg</strong></p><p><strong>Ihre Aufgaben:</strong></p><ul><li><p>Kompetente Beratung und Unterstützung relevanter Fachärzt:innen mit Schwerpunkt im Kliniksegment</p></li><li><p>Aufbau und Pflege intensiver und nachhaltiger Kundenbeziehungen - persönlich und mithilfe digitaler Kanäle</p></li><li><p>Zielgerichtete, inhaltlich fundierte Gesprächsführung, die sich auf den Nutzen für die Kunden und den Mehrwert für Patient:innen fokussiert</p></li><li><p>Enge Kooperation mit dem Medical Affairs Team, um regionale Programme und relevante Aktivitäten zur Unterstützung der Bedürfnisse von HCPs umzusetzen</p></li><li><p>Eigenverantwortliches Gebietsmanagement einschließlich Account Analysen, Tourenplanung und Dokumentation Ihrer Aktivitäten im CRM-System</p></li><li><p>Teilnahme an Messen und Kongressen sowie eigenständige Planung, Koordination und Durchführung von Fortbildungsveranstaltungen und Fachvorträgen</p></li><li><p>Regelmäßige pro-aktive & strukturierte Berichterstattung ans lokale Führungsteam</p></li></ul><p><strong>Ihr Profil:</strong></p><ul><li><p>Sie verfügen über eine abgeschlossene medizinische, pharmazeutische oder naturwissenschaftliche Ausbildung, z. B. als geprüfter Pharmareferent (w/m/d), oder haben ein relevantes (natur- oder gesundheitsökonomisches) Studium gemäß §75 Arzneimittelgesetz (AMG) abgeschlossen</p></li><li><p>Sie haben bereits Erfahrung im Außendienst für Rx Arzneimittel gesammelt</p></li><li><p>Sie verfügen über profunde Kenntnisse in der onkologischen Indikation oder über ein aktives Netzwerk in diesem Bereich</p></li><li><p>Sie haben ein gutes Verständnis von Abläufen im Klinikvertrieb sowie von den Erstattungsmechanismen im deutschen Gesundheitssystem</p></li><li><p>Sie zeichnen sich durch unternehmerisches Denken und die Fähigkeit, Win-Win Situationen zu erkennen aus</p></li><li><p>Sie arbeiten ergebnisorientiert, zeigen Eigeninitiative, Flexibilität und sehr gutes Zeitmanagement</p></li><li><p>Sie sind versiert im Umgang mit Microsoft Office und anderer gängiger Software</p></li><li><p>Sie haben ein sympathisches und gewinnendes Auftreten und eine hohe Begeisterung für den Außendienst</p></li><li><p>Ihr Wohnort liegt im relevanten Einsatzgebiet und Sie besitzen einen Führerschein der Klasse 3/B</p></li><li><p>Sie sprechen fließend Deutsch und verfügen über gute Kenntnisse der englischen Sprache</p></li></ul><p>Sehen Sie sich selbst in dieser Stellenbeschreibung? Dann bewerben Sie sich jetzt und machen Sie den ersten Schritt in Richtung „Regeneron Way“! Wir haben eine inklusive Kultur, die umfangreiche Sozialleistungen bietet, die je nach Standort variieren. In den USA können die Leistungen Gesundheits- und Wellnessprogramme (einschließlich Krankenversicherung, Zahn-, Sehkraft-, Lebens- und Berufsunfähigkeitsversicherung), 401(k)-Zusatz des Unternehmens, Familienleistungen, Aktienzuteilung, bezahlte Freistellungen und bezahlten Urlaub (z. B. Militär- und Elternzeit), für berechtigte Mitarbeiter auf allen Ebenen umfassen! Für weitere Informationen über die Leistungen von Regeneron in den USA siehe https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. Für die spezifischen Vorteile anderer Länder sprechen Sie bitte mit Ihrem Personalberater.<br>Wir sind der Meinung, dass wir bei Regeneron am erfolgreichsten sind und am besten arbeiten, wenn wir zusammen sind. Aus diesem Grund sind viele Aufgaben bei Regeneron nur vor Ort zu erfüllen. Bitte wenden Sie sich an Ihren Personalberater und Personalverantwortlichen, um weitere Informationen über die Vor-Ort-Richtlinien von Regeneron und über die Erwartungen für Ihre Rolle und Ihren Standort zu erhalten.<br> </p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 04:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Business Process Optimization]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45913]]></requisitionid>
    <referencenumber><![CDATA[R45913]]></referencenumber>
    <apijobid><![CDATA[r45913]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45913/associate-director-business-process-optimization/]]></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>The <strong>Associate Director, Business Process Optimization </strong>will serve as a strategic leader and expert practitioner driving process improvement and operational excellence. This role requires deep expertise in Lean Six Sigma (LSS), Theory of Constraints, and other process improvement methodologies combined with a proven ability to develop and scale new functional disciplines within an organization with the ability to influence peers and leaders to take the action required to achieve improved outcomes. The Associate Director will establish a new Business Transformation sub-function for process engineering, providing mentorship to scale the discipline, while leading the identification of improvement opportunities through data-driven insights, collaborating with SMEs on process optimization activities, and regularly engaging with senior leadership to ensure insights drive process improvement priorities.</p><p><strong>In a typical day, you will,</strong></p><ul><li>Identify process bottlenecks through data driven techniques, partner with SMEs in the development of process improvement plans and engage with senior leaders to drive action and achieve improved outcomes.</li><li>Leverage individual contribution by combining knowledge, skills and best-practice methods to lead data-driven process optimization.</li><li>Lead Business Process Design Activities in partnership with leadership and cross-functional Subject Matter Experts (SMEs) to evaluate current state workflows, define business requirements, and develop streamlined future state processes.</li><li>Drive business process alignment and integration across multiple transformation programs, functional areas, and other strategic initiatives</li><li>Partner with Data Analytics to establish key performance metrics and reports to evaluate process effectiveness and business value delivery</li><li>Align with Processes & Procedures to conduct process impact assessments and integrate future business processes into SOPs and controlled documentation</li><li>Support Organizational Change Management to define stakeholder impact and provide process guidance to ensure successful adoption</li><li>Collaborate with IT on technology solutions to enable effective process execution</li><li>Collaborate with Program Managers, Project Managers, and cross-functional Project Teams to drive execution of projects autonomously while ensuring alignment with business objectives</li><li>Lead the development of Process Optimization Standard Frameworks and Methodologies</li><li>Support the creation of Process Optimization Upskilling Experiences for others including leading development of Process optimization content for inclusion in the Business Transformation Community of Practice</li><li>Organize and maintain comprehensive process documentation to ensure information is accessible and secure.</li><li>Provide guidance and mentorship to junior team members in the areas of Business Process Design and Process Optimization</li></ul><p><strong>Competencies:</strong></p><ul><li><strong>Methodology and Tools</strong>: Expert Proficiency in Lean Six Sigma, Theory of Constraints and BPM software to design and implement streamlined, scalable business processes that align with organizational strategy.</li><li><strong>Systematic Thinking</strong>: Demonstrated experience in structured problem-solving and decision-making methodologies.</li><li><strong>Data Driven: </strong>Proven expertise in leveraging data analytics, advanced reporting tools, and KPI development to shape decision-making, with advanced proficiency in visualization tools like Tableau and Power BI to communicate insights effectively.</li><li><strong>Critical Thinking</strong>: Highly skilled in evaluating complex business scenarios, identifying high-impact process improvements, and aligning them with overarching strategic objectives.</li><li><strong>Logical Reasoning</strong>: Applies logical reasoning to understand and manage intricate process flows, interdependencies, and organizational dynamics effectively.</li><li><strong>Problem Solving</strong>: Expertise in diagnosing multifaceted process challenges, designing innovative solutions, and leading change initiatives to completion.</li><li><strong>Attention to Detail</strong>: Ensures rigorous evaluation of processes and outcomes, maintaining a high level of accuracy and consistency through advanced methodologies.</li><li><strong>Organizational Skills</strong>: Demonstrates exceptional organizational skills, utilizing process mapping and workflow tools to ensure clarity, scalability, and alignment with business goals.</li><li><strong>Executive Communication</strong>: Exceptional ability to articulate complex process strategies and outcomes clearly and persuasively to senior leadership and diverse stakeholders.</li><li><strong>Interpersonal Skills</strong>: Strong interpersonal and relationship-building skills to foster collaboration and alignment across cross-functional teams and executive stakeholders.</li></ul><p><strong>In order to be considered qualified for this role </strong>a minimum of a Bachelor’s Degree and 10+ years of progressive and relevant industry experience in a process development and/or process optimization role.</p><ul><li>MS in a related field or MBA Preferred.</li><li>Lean Six Sigma Black Belt Certification 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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 19:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, OT Data Management]]></title>
    <date><![CDATA[Mon, 02 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45553]]></requisitionid>
    <referencenumber><![CDATA[R45553]]></referencenumber>
    <apijobid><![CDATA[r45553]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45553/process-development-engineer-ii-ot-data-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>The Data Enablement and Analytics (DEA) team drives the future of digitalization within the Product, Analytics and Process Development (PAPD) organization. By making data usable, useful, and impactful DEA accelerates process development, supporting Regeneron’s mission to use the power of science to bring new medicines to patients over and over again.</p><p>In this role, you will enhance and maintain Operational Technology (OT) data systems, platforms, and tools that deliver high-quality data to lab specialists for real-time decision-making and offline analysis. 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><h3>Responsibilities:</h3><ul><li>Support the monitoring, maintenance and continued development of OT data systems to improve reliability, availability, and usability for manufacturing process development teams.</li><li>Ensure OT data availability, integrity, quality, security and accessibility by implementing standards, controls, and audits that reduce incidents and outages.</li><li>Assist distributed data managers in effectively defining and implementing projects, enabling teams to deliver on key objectives.</li><li>Partner with lab specialists to integrate process control and data acquisition systems into a unified architecture to advance data analytics and digital maturity.</li><li>Contribute to IT/OT convergence initiatives that improve security and compliance.</li></ul><h3>What A Typical Day in the Role Might Look Like:</h3><ul><li>Continuous Improvement: Translate user requests into prioritized feature enhancements for existing systems.</li><li>Project Management: Design, lead, and implement agile and waterfall DEA projects. Coach and guide junior resources.</li><li>Administration: Onboard new equipment. Review and manage system access requests.</li><li>Support & Maintenance: Perform software updates and patching. Proactively monitor system health issues. Troubleshoot and resolve incident reports.</li><li>Knowledge Sharing: Provide OT subject matter expertise to PAPD customers and multi-functional teams. Conduct new application evaluations and present proof-of-concept findings.</li></ul><h3>This Role May Be for You If:</h3><ul><li>You are a champion for data-driven decision making.</li><li>You uphold high standards for accuracy, quality and attention to detail.</li><li>You thrive in a team-based, multi-functional, collaborative environment, and communicate clearly with technical and non‑technical partners.</li><li>You bring a solution‑oriented mentality and can translate user requirements into scalable, secure, and maintainable data solutions.</li></ul><h3>This role requires:</h3><ul><li>BS in Computer Science, Information Systems, Biomedical/Chemical/Electrical Engineering, or related field with 7-8+ years of proven experience, or MS with 3+ years.</li><li>3+ years configuring AVEVA PI Historian and Ignition SCADA systems</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><li>Familiarity with control systems architecture, industry standards and communication protocols (ISA-95, S88, OPC, MQTT)</li><li>Working knowledge of continuous and batch manufacturing processes, associated data sources, software integration, consumption and data analytics tools</li><li>Foundational knowledge of lab-based automation software (e.g. Unicorn, Biobrain Supervise, FactoryTalk)</li><li>Growing proficiency in Python scripting</li><li>Familiarity with the concepts of Industry 4.0, digitalization, and IT/OT convergence</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>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Mar 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Hematology Oncology]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43420]]></requisitionid>
    <referencenumber><![CDATA[R43420]]></referencenumber>
    <apijobid><![CDATA[r43420]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43420/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[<p>The Senior Medical Director, Clinical Sciences, Hematology Oncology provides clinical leadership and is responsible for all clinical deliverables within the assigned section of a clinical program 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.</p><p>A day in the life may include the following responsibilities:</p><ul><li>Manages all operational aspects and drives execution of the section of the clinical program in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates.</li><li>Ensures timely execution of assigned clinical deliverables within approved budget.</li><li>Supports Program Lead MD and frequently lead 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>Supports Program Lead MD in ensuring 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>Contributes/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><li>Ensures career development of GCD colleagues through active participation in the performance management and talent planning processes. Provides on-boarding, training, and mentoring support and contributes to the performance evaluation of GCST members as appropriate.</li><li>Serves frequently as member for GCD training programs, author or reviewer for clinical SOPs. May contribute to GCD strategy by serving on taskforces or other panels.</li></ul><p>This job may be for you if you:</p><ul><li>Want to impact patients by developing new and innovative therapies</li><li>Have strong management, interpersonal, communication, negotiation, and problem-solving skills</li><li>Considerable organization awareness, including significant experience working cross functionally</li><li>Have medical/scientific expertise in the disease area of assigned program</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></ul><p>In order to be considered for this position, you must have an M.D. preferably with clinical training in a relevant disease area. 4+ years' experience in clinical research or drug development in an industry environment spanning clinical activities in Phases 1 through 4 is required.</p><p>#LI-onsite, #MDJobs, #MDJobsCD, #GDTherapeuticJobs</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>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 15:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[District Manager-Dermatology-Central California (SF, Las Vegas, Fresno & San Jose)]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44946]]></requisitionid>
    <referencenumber><![CDATA[R44946]]></referencenumber>
    <apijobid><![CDATA[r44946]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44946/district-manager-dermatology-central-california-sf-las-vegas-fresno-san-jose/]]></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>Geography: San Francisco, CA, Las Vegas, NV, Fresno, CA & San Jose, CA</strong></p><p>The District Manager (DM), Dermatology will report to the Regional Director, Dermatology and be responsible for hiring, leading, developing and retaining the Dermatology Medical Specialists in their assigned district. </p><p><strong>A Typical Might Look Like This:</strong></p><p>The DM 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 Dermatology District assigned. The DM will work closely with their Alliance partner counterpart(s) to insure full cooperation and transparency. The DM will work closely to ensure appropriate development and retention of key personnel within the district to continue to facilitate growth in the commercial organization. The DM 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>This Position Might Be for You If:</strong></p><ul><li><p>Successful leadership record of hiring, coaching, developing, promoting, and retaining top talent within span of control and ability to effectively manage performance of the team.</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a District Sales Manager in complex markets within complex systems required.</p></li><li><p>Strong understanding of Payer environment, reimbursement and challenges within National, Regional and local payer market including; government programs, managed health care and evolving health care systems.</p></li><li><p>Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners.</p></li></ul><p>To be considered for this opportunity you will have the following: Bachelor’s degree required, Master’s degree or other advanced education/certifications a plus (Focused degree in science or clinical experience is a plus). Minimum of 7 years of pharmaceutical/biopharmaceutical experience with 3 years of sales leadership/management in office-based, sub-cutaneous self-injectable biologic markets required. Experience in the Dermatology market preferred. Ability to travel extensively with local and regional influence.</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>$175,300.00 - $218,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Data Developer]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43002]]></requisitionid>
    <referencenumber><![CDATA[R43002]]></referencenumber>
    <apijobid><![CDATA[r43002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43002/principal-it-data-developer/]]></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>Principal IT Data Developer </strong><strong>(Troy, NY)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks a Principal IT Data Developer (Troy, NY) to execute the full application development</p><p>lifecycle, conception, and implementation. Participate in/lead requirements gathering, analysis and design specification development. Engage business stakeholders in value/process dialogue to develop requirements. Perform (hands-on) development, testing, and support for SharePoint, mobile, and web. Develop GxP solution documentation, flowcharts, layouts, designs, diagrams, and codes. Develop and maintain technical “product” solution roadmaps and release plans. Coordinate service levels and capture, deliver, and measure performance on requests/incidents. Lead on-shore/off-shore development and support teams. Seven (7) Direct Reports in the position of Power Platform Consultant. 25% domestic travel for internal meetings at various Regeneron facilities, and 10% international travel required to various Regeneron sites globally.</p><p>SALARY RANGE: $142,626.00 - $166,000.00 per year</p><p><strong>Job Requirements</strong><strong>:</strong></p><p>Requires a Bachelor’s degree in Computer Science, Mathematics, Electronics Engineering or related field and 6 years of hands-on development experience including leading key initiatives, colleagues, and vendors in the Pharmaceutical or Technology industry. Must have 5 years of experience leading development teams. Must have experience with: FDA GMP and GxP Computer Systems Validation; Bio-Pharmaceutical Manufacturing; Dassult Document Management and Process Management Data Systems; Blue Mountain IT Asset Management Data Systems; ServiceNow Data Systems; FileMaker Pro Application or Database Development; PowerBI, QlikSense, and Tableau Visualization Tools; SQL Server, Postgres, and Oracle Database; Microsoft Azure, Dataverse, Fabric, Azure functions, Logic Apps, and Azure App Service; Establishing and Administering Microsoft On-Premise Gateways; Microsoft DevOps, BitBucket, and Establishing CI/CD Data Pipelines; PowerApps and Power Automate; Microsoft .NET, Access, Visual Basic, SSIS and SSRS; Programming languages such as Python and #C; SharePoint 2013, 2016, O365 Designer/Workflow, Nintex, InfoPath, and Web Parts; MS SQL, jQuery, Java Script, PW Scripts, HTML, CSS, Client Object Model, and SOA; AWS EC2, RDS, and S3 Data Platforms; Electronic workflow technologies including forms and workflow approvals; iOS and PowerApps mobile development platforms; Designing and Implementing Technology Shared Services and Governance; Waterfall, Agile, and SCRUM Methodologies; ITIL & SDLC Methodologies; Data Analytics, Data Warehouse, and Business Intelligence; Leading on-shore and offshore developers; and Technology Service Catalogue Management. 25% domestic travel for internal meetings at various Regeneron facilities, and 10% international travel required to various Regeneron sites globally. Must have certifications in Microsoft Technologies such as Azure Developer Associate, Power Platform Developer Associate, SharePoint, Microsoft MCITP, or MCTS.</p><p>Apply at https://careers.regeneron.com. Reference code R43002.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 12:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Corporate Counsel (Information Technology Transactions)]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45249]]></requisitionid>
    <referencenumber><![CDATA[R45249]]></referencenumber>
    <apijobid><![CDATA[r45249]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45249/director-corporate-counsel-information-technology-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>As a member of the Contracts Group in the Regeneron Law Department’s Transactions Law Group, the Director, Corporate Counsel will draft, review and negotiate a wide array of contracts for Regeneron’s Information Systems and Technology operating teams and provide related advice and counsel. The level of counseling requires a solid understanding of general business transactions and related legal issues, outstanding drafting and negotiation skills and a strong understanding of, or desire to learn about, information technologies, data privacy, and artificial intelligence. Experience in life sciences is preferred. The role will have a direct impact on facilitating our science and research.<br><br><strong>As a Director, Corporate Counsel, a typical day may include:</strong></p><ul><li><p>Drafting, negotiating and bringing to execution cloud (SaaS/PaaS/IaaS) and software license agreements, hybrid cloud agreements, and consulting and professional service agreements critical to Regeneron's operations throughout the company.</p></li><li><p>Providing legal support and counsel for software applications, data feeds and analytics, infrastructure applications, information security, telecommunications and telephony, consumer-facing apps, and other information technology tools used throughout Regeneron, including for research, development, clinical, manufacturing, commercial, and general administrative services organizations, whether as discrete applications or as an integrated enterprise resource planning platform, often as a licensee of the technology and within a regulated environment.</p></li><li><p>Advising on artificial intelligence to the business and interacting with the AI Governance Committee</p></li><li><p>Advising on other current and potential legal and commercial issues with industry specific knowledge and transactional guidance</p></li><li><p>Working collaboratively with other organization groups, including the Privacy Group and the Compliance Group, Risk Management and Global Procurement.</p></li><li><p>Advising internal clients on Regeneron’s contracts policies and practices and applicable laws.</p></li><li><p>Counseling client business teams on applicable legal risks and statutes.</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Excel at advising clients regarding all aspects of contract law, technology and related areas.</p></li><li><p>Have a history of self-motivation and working independently on projects, while meeting deadlines and prioritizing multiple matters.</p></li><li><p>Are curious and eager to learn</p></li><li><p>Possess excellent contract drafting and negotiation skills, oral and written communication skills, and strong interpersonal skills.</p></li><li><p>Can work effectively and professionally with colleagues and clients at all levels of the organization.</p></li><li><p>Enjoy working in a collaborative, team-oriented environment.</p></li></ul><p><strong>To be considered for this position, you must possess:</strong></p><p>A BA/BS and JD with excellent law school credentials. Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel is preferred. 4 to 10 years legal experience at a law firm and/or in-house, including strong corporate law experience. Possess outstanding oral and written communication skills, including significant presentation capabilities. An attention to detail and appetite for learning. Familiarity with information technology, life sciences and privacy law and experience negotiating from a licensee position are all pluses. <br><br> </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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Charleston-WV]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45098]]></requisitionid>
    <referencenumber><![CDATA[R45098]]></referencenumber>
    <apijobid><![CDATA[r45098]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45098/medical-specialist-i-dermatology-charleston-wv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Charleston]]></city>
    <state><![CDATA[West Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Charleston/Morgantown, WV</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Délégué(e) Hospitalier(e) Immunologie – Pays de la Loire & Poitou-Charentes]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45999]]></requisitionid>
    <referencenumber><![CDATA[R45999]]></referencenumber>
    <apijobid><![CDATA[r45999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45999/delegue-e-hospitalier-e-immunologie-pays-de-la-loire-poitou-charentes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>As an Immunology Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, while covering <strong>Pays de La Loire & Poitou-Charentes</strong>. </p><p>You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>Immunology Pharmaceutical Representative – Pays de la Loire & Poitou-Charentes</strong></p><p><strong>As an Immunology Pharmaceutical Representative, a typical day might include the following:</strong></p><ul><li><p>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.</p></li><li><p>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</p></li><li><p>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</p></li><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</p></li><li><p>Leverage all communication channels including digital channels, 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 Immunology leadership team</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</p></li><li><p>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</p></li><li><p>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</p></li><li><p>You can operate effectively in a “start-up” model as this is a completely new team.</p></li></ul><p>To be considered for this opportunity you must hold a Carte Professionnelle with minimum <strong>5+ years of pharmaceutical sales experience in Immunology</strong>. You are happy with regular travel and have a valid driver's license. Conversational English would be desirable, but not required.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 04:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, QA Microbiology]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46191]]></requisitionid>
    <referencenumber><![CDATA[R46191]]></referencenumber>
    <apijobid><![CDATA[r46191]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46191/executive-director-qa-microbiology/]]></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 hiring! The Executive Director, QA Microbiology is responsible for the development and execution of the strategy and plan for the Regeneron GMP Microbiology program. The individual in this position is also responsible for providing direction to the function areas to ensure high-quality, safe, and effective products that are compliant with global regulatory expectations with respect to microbiological topics. This position will direct the efforts of the applicable functional areas in support of compliance and business objectives and will ensure that the Microbiology program remains current with industry expectations and help liaison with subject matter experts within the lines of businesses. </p><p>In this role, a typical day might include the following:</p><ul><li><p>Implement a value-added microbiology program based on sound science and the application of the appropriate quality, regulatory and legal requirements.</p></li><li><p>Monitor the performance of the microbiology program using the appropriate metrics and demonstrate a commitment to continuous improvement.</p></li><li><p>Embed quality tools and risk management processes within the microbiology program.</p></li><li><p>Stay abreast of changing requirements/expectations and proactively address within the microbiology program.</p></li><li><p>Use quality and risk management tools to make timely, science-based decisions to protect patient safety.</p></li><li><p>Implement appropriate solutions that address complex technical, legal and global regulatory standards.</p></li><li><p>Partners with QA Operations functions within the lines of business to translate strategy to implementation, and ensure compliant and robust aseptic practices.</p></li><li><p>Demonstrate confidence during difficult decision-making and influence internal and external business partners to ensure acceptable outcomes.</p></li><li><p>Lead as microbiology decision maker to ensure the safety and effectiveness of the products.</p></li><li><p>Represent as the face of Regeneron to internal and external stakeholders, including regulatory agencies and corporate partners regarding microbiological topics.</p></li><li><p>Translate the vision and business strategies of the microbiological program into executable action plans.</p></li><li><p>Ensure the Microbiological Control Strategy is transparent and the organization is engaged in its execution.</p></li><li><p>Allocate resources based on microbiology program priorities and corresponding business needs.</p></li><li><p>Establish high standards for performance management and accountability to achieve microbiological and organizational objectives.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Comprehensive knowledge of microbiological expectations throughout drug development process, pharmaceutical technology, drug manufacturing processes and related issues, drug laws, global regulations, and guidelines, particularly CMC and GMP.</p></li><li><p>Experience building up a quality culture and quality management capabilities.</p></li><li><p>Comprehensive knowledge and experience in CMC section content for investigational and marketed product submissions (IND, BLA, CBE, PAS) for FDA and equivalent submissions for Europe.</p></li><li><p>A sense of passion and commitment for delivering things as quickly and efficiently as possible.</p></li><li><p>The ability to think and operate in a rapidly evolving and ambiguous environment.</p></li><li><p>Ability to articulate and execute concepts for developing and ensuring the highest quality throughout the network (internal and external).</p></li><li><p>Intellect for quality risk identification, mitigation, and management.</p></li><li><p>Strong communication skills —written and oral.</p></li><li><p>Experience with businesses in different phases of the business lifecycle and the quality and validation issues associated with these phases.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Engineering, Chemistry, Biology or related science/technical field and the following amount of experience in a regulated industry (ie., Biotech, Pharma, Medical Device) for each level:</p><ul><li><p>Sr Director – 15+ years</p></li><li><p>Executive Director – 18+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role. Equivalent combination of education and experience will be considered.</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>$239,600.00 - $399,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 10:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Device Development Engineer (Project Leadership)]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44517]]></requisitionid>
    <referencenumber><![CDATA[R44517]]></referencenumber>
    <apijobid><![CDATA[r44517]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44517/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>Regeneron is seeking a Device Development Engineer to join our project lead team. The 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>A typical day for a Device Development Engineer might include:</p><ul><li><p>Leads multidisciplinary engineering project teams (Human Factors, V&V Engineering, Manufacturing Engineer, Quality Engineering) through the complete device design and development lifecycle of a combination product development within the Regeneron Pipeline.</p></li><li><p>Defines detailed product requirements and specifications with commercial, clinical, and other development/strategy collaborators.</p></li><li><p>Defines technical specifications and design requirements in collaboration with engineering teams (manufacturing, verification, packaging etc.)</p></li><li><p>Responsible for all user needs and requirements to be validated through design and development.</p></li><li><p>Develops, manages, and communicates development program plans, risks, timelines, and budgets to internal and external team members.</p></li><li><p>Integrate device development activities with Chemistry Manufacturing Controls (CMC) and Global development timing and goals.</p></li><li><p>Supports global internal manufacturing and external manufacturing teams around relevant design and process development information transfers.</p></li><li><p>Leads all aspects of product testing and quality assurance processes for the specific device development.</p></li><li><p>Ensures comprehensive and compliant Design History File (DHF) is developed and ensures to meet regulatory and quality requirements (21CFR Part 3 and 21 CFR 820.30).</p></li><li><p>Supports management in related clinical and commercial regulatory activities that is related to the device development (ie: IND/IMPD, BLA Submission, Clinical Pharmacy Manuals etc.)</p></li><li><p>Understands design inputs and outputs of multiple delivery systems and how it can impact end users.</p></li><li><p>Supports management and/or therapeutic area device project leads, in strategic product launch and go-to-market plans for the device development.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Understand relevant FDA regulations, particularly 21 CFR Part 3 and 21 CFR 820.30.</p></li><li><p>Have experience with design history file management (21 CFR 820.30), is a plus.</p></li><li><p>Possess strong project management and interpersonal skills and strong analytical and problem-solving capabilities.</p></li><li><p>Can balance business objectives with technical constraints.</p></li><li><p>Can work effectively across multiple functional teams.</p></li><li><p>Enjoy working in a fast-paced, multifaceted research and development environment.</p></li><li><p>Are willing and able to travel for partner meetings, audits, and project coordination activities.</p></li></ul><p>To be considered for the Device Development Engineer you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a B.S in Engineering. For various levels you must have the following:</p><ul><li><p>Device Development Engineer: 2+ years of relevant experience</p></li><li><p>Sr. Device Development Engineer: 5+ years of relevant experience</p></li></ul><p>Previous experience in product management/project management/ and/or project leadership related activities is preferred. Level is determined based on qualifications relevant to the role.</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>$75,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 14:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Associate Scientist, Sample Management]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46177]]></requisitionid>
    <referencenumber><![CDATA[R46177]]></referencenumber>
    <apijobid><![CDATA[r46177]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46177/sr-associate-scientist-sample-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>The Automated Biobanking Core is seeking a Senior Associate Scientist to support and advance automated and manual sample management operations. This position plays a key role in sustaining high-throughput biospecimen storage, retrieval, and distribution workflows while ensuring equipment reliability, operational continuity, and high-quality scientific support across Regeneron’s research and development programs. The successful candidate will work independently with automated systems, collaborate with cross-functional groups, and contribute to continuous improvement initiatives aimed at enhancing sample management efficiency and system performance.</p><p>As a Sr Associate Scientist, a typical day may include:</p><ul><li><p>Independently operate automated biospecimen storage and retrieval systems and liquid handlers.</p></li><li><p>Troubleshoot and resolve system errors; perform routine maintenance and calibrations to ensure optimal performance.</p></li><li><p>Monitor, document, and trend equipment performance to keep systems within defined specifications and uptime targets.</p></li><li><p>Support manual and automated sample management and distribution workflows, ensuring continuous operation of automated cold‑storage technologies.</p></li><li><p>Serve as a primary point of contact for ABC; coordinate with internal partners, IT, and external vendors to support clinical programs and collaborations and to resolve operational issues promptly.</p></li><li><p>Partner with IT to develop and enhance software interfaces and data acquisition platforms supporting sample management.</p></li><li><p>Identify, evaluate, and implement new strategies and technologies to improve workflow efficiency and system performance.</p></li><li><p>Train and mentor sample management personnel on automated systems and best practices.</p></li><li><p>Promote a safe, clean, and organized laboratory environment; adhere to safety requirements and proactively address potential issues.</p></li><li><p>Communicate progress and results effectively; present at team and cross-functional meetings; model professionalism, integrity, and a strong work ethic; engage in ongoing professional development.</p></li></ul><p>To be considered, you must meet the following requirements:</p><ul><li><p>Bachelor’s degree in Engineering or a Life Sciences discipline.</p></li><li><p>Minimum 5 years of industry or relevant field experience.</p></li><li><p>Experience with manual and automated sample management technologies and workflows (e.g., automated cold storage, retrieval systems, liquid handling platforms).</p></li><li><p>Strong written and oral communication skills with the ability to collaborate across a matrixed organization.</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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46369]]></requisitionid>
    <referencenumber><![CDATA[R46369]]></referencenumber>
    <apijobid><![CDATA[r46369]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46369/drug-production-associate-manufacturing-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 Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. 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>A typical day for a Drug Production, Associate Manufacturing Specialist might include:</p><ul><li><p>Performing all aspects of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operating automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Supporting equipment start-up, troubleshooting, and validation</p></li><li><p>Partnering with R&D teams to implement new drug manufacturing processes and technologies</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Enjoy working 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>Are highly organized, detail oriented and perform work accurately the first time</p></li><li><p>Value trust and transparency in everyday work</p></li><li><p>Work well in both small and large teams to accomplish tasks adhering to a schedule</p></li><li><p>Can 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>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Are a good communicator and can give and receive feedback constructively</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>Gowning and Environment</p><ul><li><p>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>Shift & Physical Requirements</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.</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>To be considered for this role you must meet the below minimum education and experience requirements:</p><p>Drug Production, Associate Manufacturing Specialist:</p><ul><li><p>HS diploma + 4 years of relevant work experience <strong>or</strong></p></li><li><p>AS, BS or BA in Life Sciences or related field</p></li></ul><p>Regeneron offers an exciting and competitive benefits package! For details check out: <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a></p><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 (hourly)</strong></strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Predictive Analytics]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44966]]></requisitionid>
    <referencenumber><![CDATA[R44966]]></referencenumber>
    <apijobid><![CDATA[r44966]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44966/associate-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>We are seeking a highly motivated and talentedAssociate Manager of Predictive Analytics to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop and apply predictive models on the world’s largest integrated datasets of genomics, proteomics, and electronic medical records. </p><p><strong>The role involves partnering with cross-functional teams, including Business Development, Laboratory staff, and other scientific groups, to foster collaboration and advance key initiatives. The candidate mush have the ability to influence, with strong interpersonal skills. Excellent communication and interpersonal skills are also required as this candidate will be expected to work productively in a collaborative, team working environment. </strong></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Plan, develop, and execute large-scale analyses of proteomic and genomic datasets, with an emphasis on aging and age-related diseases.</li><li>Develop and implement methods for data harmonization and normalization across distinct cohorts to ensure consistency and reproducibility of results.</li><li>Evaluate statistical methods for disease risk prediction, and if necessary develop new method</li><li>Stay informed on emerging market trends in disease prediction and applications of genomics data to continuously refine research directions</li><li>Deliver clear and concise presentations of genomics and proteomic findings to leadership, ensuring alignment with organizational goals and priorities</li><li>Ability to provide data to internal, external, and non-scientific audience</li><li>Design, implement, and optimize data pipelines for high-throughput genomic and proteomic workflows, ensuring efficient processing of large-scale proteomic datasets.</li><li>Develop and integrate robust quality control (QC) measures at multiple stages of analysis pipelines to ensure data accuracy, consistency, and reproducibility</li></ul><p><strong>This role might be for you if have:</strong></p><ul><li><p>Demonstrated expertise in statistics, machine learning and predictive analytics applied to biological data.</p></li><li><p>Demonstrated aptitude for translating research results into products or prototypes</p></li><li><p>Proven ability to independently lead and manage 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>Demonstrated ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li>A PhD in a relevant field (e.g., human genetics, statistics, computational biology, or related disciplines), or a Bachelor’s Degree with at least four years of experience in analyzing large-scale genomics dataset</li><li>Candidates with prior industry experience are preferred</li><li>Experience in exploratory data analysis, applied statistics, or software engineering is preferred in one or more of these domains</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Cloud DevOps Engineer]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46267]]></requisitionid>
    <referencenumber><![CDATA[R46267]]></referencenumber>
    <apijobid><![CDATA[r46267]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46267/lead-cloud-devops-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>Lead Cloud DevOps Engineer (Tarrytown, NY)</strong></p><p>Regeneron Genetics Center LLC seeks a Lead Cloud DevOps Engineer to deploy reliable infrastructure services on AWS, from the ground up, to deliver highly scalable services. Interact with Regeneron scientist to understand their computational needs and develop solutions to fasten their research. Provide support and perform systems administration tasks. Develop solutions to parallelize the legacy/standalone jobs and run them on distributed computational platforms. Apply industry standards to ensure system and application security. Drive automation of operations and management of infrastructure as code. Deploy and lead monitoring, metrics, and logging capabilities on cloud engineering platforms. Lead effort to containerize various applications and tools and implement container orchestration. Develop SOPs and configure cloud services to stand up high compute pipelines. Install, configure, and</p><p>maintain cloud applications and services. Keep abreast of the latest advances in the cloud platforms and services. Provide leadership for cloud DevOps engineers. Interact with key partners to clearly define and iterate on requirements. Provide end user support, training, and documentation. Telecommuting permitted. 20% domestic travel required to visit Regeneron office to meet with Business users, rest of Team and conferences.</p><p>SALARY RANGE: $160,805.00 - $210,000.00 per year</p><p><strong>Job Requirements:</strong></p><p>Requires a Master’s degree in Computer Science, Information Systems, Information Assurance, or a related field and 2 years of Information Technology cloud engineering and DevOps experience. Must have experience with: Amazon Web Service (AWS) Cloud Services; Containers and orchestration services such as docker, ECS, ECR, EKS; Fargate and systems administration of Linux servers; Ubuntu workstations, Patching, backup, upgrades, and PAM authentication; CloudFormation scripts to automate the server deployment and configuration; EC2, EBS, S3, ELB, RDS, and monitoring tools; and Web server administration – Tomcat, Apache, and Nginx. 20% domestic travel required to visit Regeneron office to meet with Business users, rest of Team and conferences.</p><p>Apply at <a href="https://careers.regeneron.com">https://careers.regeneron.com</a>, reference code R46267.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42034]]></requisitionid>
    <referencenumber><![CDATA[R42034]]></referencenumber>
    <apijobid><![CDATA[r42034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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 at our SUNY 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>As an HVAC Technician, a typical day might include the following:</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></ul><p>This role might be for you if you:</p><ul><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>To be considered for the HVAC Technician you ideally should have an 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>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 (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Tue, 21 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43330]]></requisitionid>
    <referencenumber><![CDATA[R43330]]></referencenumber>
    <apijobid><![CDATA[r43330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43330/director-clinical-scientist-hematology/]]></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>The Director Clinical Sciences, Hematology, leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and late phase development. The Director reports to the Senior Director Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. The director will be responsible for managing a team of clinical scientists.</p></div><div><div><div><div><p>As a Director in Hematology, a typical day may include the following:</p><ul><li><p>May function as lead Clinical Scientist (CS) for program, and/or as delegate of Therapeutic area (TA) Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Line Manager for CS team and serves as key functional advisor or representative for the CS group; ensures alignment of process and procedures for CS across assigned assets/programs in alignment with TA expectation; Guides assigned Program teams/direct reports</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>Applies advanced scientific expertise to propose, design, and execute clinical research and development studies for early and late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>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 independently supports the development of regulatory documents; performs quality review and/or approval; adjudicates and resolve cross functional comments independently; Independently leads planning and prepares information for external /stakeholder meetings (IM, Governance, IDMCs, Regulatory Authorities)</p></li><li><p>Performs and mentors direct reports in clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Applies advanced analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies; Identifies areas of potential inconsistent data review</p></li><li><p>Ensures consistent first line medical/clinical data review techniques and conventions across studies/programs; leads drafting/updating/review of clinical data review plan and medical monitoring plans; ensures execution where appropriate for assigned studies/programs</p></li></ul><p>This role may be for you if:</p><ul><li><p>Exhibits high level of skill in building team and mentoring direct reports</p></li><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to influence within team and department and may influence across functionally</p></li><li><p>Demonstrates exceptional initiative, creativity and innovation skills. Directly contributes to the development of innovations. Identifies opportunities to initiate operational changes</p></li><li><p>Strong direct-line and cross-functional management, interpersonal and problem-solving skills</p></li></ul><p>To be considered for this position, you must have a bachelor’s degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). Additionally, ≥ 10 years of pharmaceutical clinical drug development experience. We are specifically seeking experience with lymphoma/hematology oncology, and a minimum of 4 years of direct and/or indirect management experience. Proven understanding of therapeutic disease areas and drug candidates including underlying disease biology, clinical manifestations and therapeutic standard practice, compounds including mechanism of action and drug landscape. Other levels considered depending on experience. #Hematology</p></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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$202,000.00 - $336,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director and Corporate Counsel, Regulatory & Commercial Product Attorney]]></title>
    <date><![CDATA[Wed, 14 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44229]]></requisitionid>
    <referencenumber><![CDATA[R44229]]></referencenumber>
    <apijobid><![CDATA[r44229]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44229/director-and-corporate-counsel-regulatory-commercial-product-attorney/]]></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 position with the Regeneron Regulatory and Commercial Law team will provide proactive and collaborative legal advice and counsel in connection with the commercialization of one or more of Regeneron’s products, and be part of a legal team supporting cardiovascular, hematology, rare disease, oncology, obesity, and new products. Counsel will be embedded as a core team member, serving as a strategic legal advisor to multiple internal stakeholders, including the commercial, medical affairs, regulatory, HEOR, corporate affairs, and compliance teams. Counsel will advise our internal partners through a deep understanding of (i) the complex laws and regulations and (ii) business and strategic objectives related to the discovery, development, and commercialization of biotechnology products.</p><p><strong>This role is based at Regeneron's offices in Sleepy Hollow, NY (4 days a week onsite) - it is not open to hybrid or fully remote assignments</strong></p><p>A<strong> typical day may include:</strong> <strong>:</strong></p><ul><li>Providing day-to-day strategic and business-focused legal and risk counseling for one or more of Regeneron’s products/product candidates, from development through commercialization, including advising on a broad range of healthcare regulatory matters, including regulatory labeling discussions, advertising and promotion, drug safety, market research, scientific exchange, and interactions with healthcare professionals and patients.</li><li>Demonstrating a solid understanding of the strategic and tactical objectives of the client teams supported, and advising on strategic brand and medical planning, developing creative and innovative solutions to key initiatives, considering the business objectives and priorities, as well as the US and/or international legal and regulatory landscape.</li><li>Counseling on all aspects of product commercialization, including launch preparation, launch execution, market development, disease awareness, product communication, advertising and promotion, and strategic brand planning.</li><li>Ensuring compliance with all relevant laws, regulations, policies, procedure and controls within relevant business areas supported</li><li>Advising on data disclosures following clinical development milestones via press releases and US or international medical congresses and scientific exchange compliant with applicable laws and regulations.</li><li>Liaising with other Law Department functions both in the US and globally, including litigation, IP, Compliance, and Transactions, to ensure integrated legal support and timely updates and information sharing.</li><li>Reviewing relevant draft scientific publications and providing guidance as appropriate.</li><li>Providing additional legal support on various matters for the Regulatory and Commercialization Law Team.</li></ul><h3><strong>This role may be for you if you have</strong>:</h3><ul><li>Possess a solid understanding of the biotech/pharmaceutical industry, including product development, commercialization, and the legal and regulatory environment (including healthcare fraud and abuse, anti-kickback, and competition law) as practiced by a multinational pharmaceutical manufacturer</li><li>Deep knowledge of applicable statutory and regulatory frameworks governing the sale and marketing of biopharmaceuticals</li><li>Ability to handle multiple priorities in a dynamic and evolving environment</li><li>Excellent oral and written communication skills with a shown ability to present complex information accurately and concisely to influence others at all levels of management</li><li>Proven capacity to cultivate strong client relationships and influence leadership, including ability to assess and help business colleagues handle risks in a highly regulated environment</li></ul><p><strong>To be considered for this role, we are looking for candidates with</strong></p><ul><li>Have a JD with excellent law school credentials</li><li>Be licensed to practice law in New York or be eligible for licensure as a registered in-house counsel</li><li>Have at least 5 years of legal experience at a nationally recognized law practice in the area of pharmaceutical and healthcare law or as an in-house attorney at a biotech/pharmaceutical company.</li><li>Previous experience as a product attorney at a pharmaceutical or biotechnology company preferred</li></ul><p><strong>Additional Information:</strong></p><ul><li>Some travel is required (US and limited international)</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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 15 Jan 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs- Thoracic Oncology/Pan Tumor (NJ, PA, DE, DC)]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44306]]></requisitionid>
    <referencenumber><![CDATA[R44306]]></referencenumber>
    <apijobid><![CDATA[r44306]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44306/associate-director-field-medical-affairs-thoracic-oncologypan-tumor-nj-pa-de-dc/]]></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>As an Associate Director, Field Medical Affairs Thoracic/Pan-Tumor Oncology you will deliver on strategies and plans of action related to our Medical Affairs oncology disease states and treatments consistent with principles of scientific exchange. We develop and maintain a list of therapeutic area experts highly relevant to oncology providing any required documentation related to these interactions. We collaborate with Clinical Development supporting the development of oncology pipeline and marketed products. Our Field Medical team communicates relevant scientific data to oncology experts/healthcare care providers and internal team members, including medical insights from Oncology scientific community.</p><p><strong>Territory</strong>: PA, NJ, DE, DC</p><p><strong>A typical day may include the following:</strong> <br>• Participate in the development and management of company sponsored clinical trials. <br>• Review of concept proposals and development of protocols.<br>• Identifies and assists in selection of investigators and trial sites.<br>• Supports site initiation and enrollment activities.<br>• Acts as a scientific resource for area healthcare professionals within the trial site community.<br>• Establish scientific relationships with investigators and internal Medical Affairs, supports investigator-initiated study (IIS) program.<br>• Identifies gaps in research needs of company 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 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>• Attend medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence with the purpose of informing internal collaborators.<br>• Assists with management of clinical data to ensure rapid and accurate communication of scientific/clinical results through support of abstract, poster, presentation, and manuscript development.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><p><strong>This may be for you if you: </strong><br>• Enjoy working independently in the field, while having an impact on our mission.<br>• Are passionate about developing knowledge of and sharing clinical scientific data<br>• Like working corroboratively and developing relationships in academic and clinical practice settings<br>• Want to have an impact on patient lives</p><p>To be considered for this an advanced Clinical/Science Degree required (MD, PharmD, PhD) is required. A minimum of 5 years related work experience in Oncology as a Field Medical Affairs representative or Medical Science Liaison required. Residence must be within the assigned territory.</p><p>#msl #medicalscienceliaison<br> </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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Drug Development Program Management]]></title>
    <date><![CDATA[Tue, 13 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44570]]></requisitionid>
    <referencenumber><![CDATA[R44570]]></referencenumber>
    <apijobid><![CDATA[r44570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44570/manager-drug-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>With guidance, this role M<strong>anager, Development Program Management </strong>uses program management knowledge and experience in the drug development industry to provide operational leadership and manage components of development program(s). This individual contributes to the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and track the execution of these plans from preclinical through commercialization/lifecycle management. </p><p><strong>A typical day in this role looks like:</strong></p><ul><li><strong>Development Teams: </strong>Under the direction of their manager or DPM Lead, supports select subteam and/or functional area meetings. May lead functional area and/or working group meetings. Participates in development of risk management plans. Tracks deliverables, risks, and issues.</li><li><strong>Business Acumen: </strong> Under direction of their manager or DPM Lead, Identifies stakeholders across organization to facilitate cross functional reviews/alignments of key documents. Manages project management planning systems (MS Project, SharePoint) for assigned programs/projects. Uses systems and tools to move the program and business forward. </li><li><strong>Communication: </strong>Facilitates collaboration on selected assignments between functional areas to ensure effective, accurate, and timely scientific/technical and program-related communication. Keeps manager and other stakeholders informed to ensure alignment of key decisions/actions items of the assigned projects. Escalates issues/risks to appropriate stakeholders in a timely manner. </li><li><strong>Problem Solving: </strong>Supports the team and lead DPM in gathering information relevant to issues and formulating solutions to issues encountered during project implementation. With direction, supports development of processes and tools to document issues and their resolution. Escalates complex problems or issues to lead DPM in a timely and appropriate manner </li><li><strong>Leadership:</strong> Influences within workstream and/or sub-sets of project team. Builds relationships and effectively collaborates with department and cross-functional colleagues. Seeks out support for resolution of conflicts.</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Are action oriented and organized</li><li>Intellectually curious</li><li>Comfortable dealing with ambiguity</li><li>Demonstrate good judgement</li><li>Think critically</li><li>Communicate and collaborate well</li><li>Are a team player </li><li>Regularly demonstrate professional maturity, and take setbacks and constructive criticism well.</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree is required and 5+ years of relevant project management experience, preferably in the drug development/pharmaceutical industry.</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 21 Jan 2026 22:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44950]]></requisitionid>
    <referencenumber><![CDATA[R44950]]></referencenumber>
    <apijobid><![CDATA[r44950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44950/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>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><div><div><div><div><div><p><strong>In this role, a typical day might include:</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></ul><p><strong>This role might be for you if can/have:</strong></p><ul><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>To be considered for this opportunity, you must have the following:</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></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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement - Supplier Relationship Management]]></title>
    <date><![CDATA[Wed, 04 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R40566]]></requisitionid>
    <referencenumber><![CDATA[R40566]]></referencenumber>
    <apijobid><![CDATA[r40566]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r40566/director-global-procurement-supplier-relationship-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>The Director, Global Procurement – Supplier Relationship Management (SRM) will be responsible for designing, implementing, and ensuring the success of the supplier relationship management framework across Global Procurement. The role will also be accountable to manage key enterprise suppliers working closely with the CPO and other stakeholders across Regeneron to manage strategies to deliver long term value creation. This leader will support Category teams to ensure optimal performance of the SRM Framework to drive innovation, manage risk, and enhance value delivery across the program. In addition the role will enable communication to suppliers and, within Global Procurement, and across Regeneron stakeholders related to SRM and other key Regeneron/Global Procurement priorities.</p><p><em><strong>This role will require 4 days per week onsite at Regeneron's offices; which may include Warren, NJ with </strong></em><strong><em>2 days per week required in our Global HQ in Tarrytown</em></strong>. <em><strong>This is not available as a fully remote / hybrid work.</strong></em></p><p>As the Director, Global Procurement - SRM, a typical day may include:</p><ul><li>Developing and leading SRM Strategy across Global Procurement, including design and execution of a comprehensive global SRM strategy, establishing ways of working and governance model across the enterprise.</li><li>Serve as the executive point of contact for key enterprise suppliers. Facilitate regular business reviews and strategic planning sessions to foster collaboration and innovation.</li><li>Drive supplier-enabled innovation initiatives and continuous improvement programs that enhance efficiency, quality, and cost-effectiveness.</li><li>Identify and mitigate supplier risks, ensuring business continuity and adherence to regulatory, legal, and ethical standards in all supplier relationships.</li><li>Leverage SRM technologies, analytics tools, and dashboards to gain insights, streamline processes, and support strategic decision-making.</li><li>Lead the development of SRM capability across Global Procurement, fostering a high-performance culture focused on collaboration, accountability, and strategic thinking..</li><li>Researching external data sources to understand industry trends, regulations and best practices to improve Regeneron’s SRM program.</li></ul><p>This role may be for you if you have:</p><ul><li>Demonstrated knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization</li><li>Deep understanding of SRM best practices and their application in a complex, regulated, and global environment.</li><li>Strong negotiation, analytical, and strategic thinking skills.</li><li>Capability to build influential relationships with stakeholders and suppliers to drive results for Regeneron.</li><li>A successful record of leading cross-functional teams to drive results through supplier relationship management efforts.</li><li>High drive to operate with integrity, focus, and clarity in an environment of ambiguity to drive change and improvement.</li><li>Working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</li><li>Ability to leverage standard business applications for communicating, presenting and analyzing (Word, Excel, PowerPoint)</li></ul><p>To be considered for this role you must posses a Bachelor's degree in a relevant field of study plus 10 - 15 years progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma. Experience successfully leading global teams, processes, and suppliers across a breadth of categories.</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>$180,400.00 - $300,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Feb 2026 18:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Commercial Operations - Oncology]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44699]]></requisitionid>
    <referencenumber><![CDATA[R44699]]></referencenumber>
    <apijobid><![CDATA[r44699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44699/manager-commercial-operations-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are recruiting a <strong>Commercial Operations Manager</strong> in the oncology field. In this critical role, you will actively plan and manage support systems for the sales and marketing teams to execute commercial strategies while driving continuous process improvement. Reporting to the Commercial Operations Associate Director, you will play a vital role in optimizing operations in a fast-paced and ever-changing environment. If you are passionate about creating business impact while collaborating with internal and external stakeholders, we encourage you to join our team.</p><div></div><p><strong>■ Job Responsibilities:</strong></p><ul><li>Collaborate with the marketing and IT teams to oversee governance and content management of promotional materials and product websites, ensuring compliance with medical, legal, and regulatory (MLR) reviews.</li><li>Coordinate with internal and external stakeholders on operational aspects of various collaborations with healthcare professionals, such as advisory boards and consulting agreements.</li><li>Work closely with the Meetings & Event Management team to arrange oncology-related conferences, sponsorships, and events for smooth execution.</li><li>Partner with local and cross-market analytics teams to execute field size adjustments, targeting, and segmentation.</li><li>Continuously improve commercial operational processes to ensure quality and scalability that align with future organizational growth.</li><li>Manage the creation and distribution of websites and commercial materials, ensuring proper internal reviews and approvals are obtained before implementation.</li></ul><div></div><p><strong>■ Ideal Candidate Profile:</strong></p><ul><li>Excels in a collaborative environment and has a talent for coordinating with cross-functional teams, including vendors and field-based employees.</li><li>Possesses strong execution and project management skills, capable of balancing multiple projects while delivering results within deadlines.</li><li>Skilled in data visualization and storytelling, with the ability to convert insights into strategies.</li><li>Proficient in tools such as Microsoft PowerPoint, Excel, Word, Veeva, and has intermediate English communication skills.</li><li>Has a strong understanding of the Japanese biopharmaceutical market and a keen interest in the oncology field.</li><li>Enjoys working in a rapidly changing environment and is committed to continuous improvement.</li></ul><div></div><p><strong>■ Requirements:</strong></p><ul><li>Experience in business process improvement and operation in healthcare companies as internal staff, or as a consultant.</li><li>A total of 7+ years of relevant work experience.</li><li>Business-level English proficiency in both spoken and written communication.</li><li>Bachelor’s degree.</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 02:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist 1 - Dermatology - Salt Lake City]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44978]]></requisitionid>
    <referencenumber><![CDATA[R44978]]></referencenumber>
    <apijobid><![CDATA[r44978]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44978/medical-specialist-1-dermatology-salt-lake-city/]]></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>Geography: Salt Lake City, Utah</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>As a Medical Specialist 1, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Imaging Operations]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44913]]></requisitionid>
    <referencenumber><![CDATA[R44913]]></referencenumber>
    <apijobid><![CDATA[r44913]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44913/senior-manager-clinical-imaging-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>As a Clinical Imaging Operations Lead, you will have a leading role in the design and execution of key strategic and operational aspects of complex early and late phase clinical trials across multiple therapeutic areas, where imaging is a primary or key endpoint. You will collaborate with Clinical Imaging Science Leads and be fully integrated within clinical study teams to ensure high-quality image acquisition, data integrity, and compliance with all study specific procedures. You should expect to work closely with our imaging vendor partners, the clinical operations function, the data management function, external clinical research organizations (CROs), and clinical sites to ensure the successful completion of startup activities, ongoing execution, and close-out of clinical studies. </p><p><strong>A day in the life may look like:</strong></p><ul><li><p><strong>Portfolio Oversight: </strong>Responsible for the execution, functional reporting, and imaging operational oversight of specific portfolios/assets through direct study management or indirect guidance of other team members working on the portfolio. Expected to develop an in-depth knowledge aligned to the portfolio and close relationships with cross-functional colleagues in similar supporting roles. </p></li><li><p><strong>Imaging Startup and Project Management Support:</strong> Collaborate with clinical operations study leads and cross-functional teams to manage the start-up activities of imaging components in clinical trials. Assist with imaging vendor selection, request for proposals, management, and performance tracking. </p></li></ul><ul><li><p><strong>Study Documentation and Compliance:</strong> Author, review, and/or manage essential study documents such as Imaging Manuals, Independent Review Charters, Communication plans, data transmittal forms, Standard Operating Procedures, and Work Instructions. Ensure all documentation is audit-ready and filed appropriately in the Trial Master File (TMF).</p></li><li><p><strong>Site Management and Training:</strong> Provide technical support and training to clinical site personnel, which may include conducting site initiation visits or Teleconferences. Review and approve training materials for imaging facilities and/or clinical site personnel. </p></li><li><p><strong>Process & Technology Improvement:</strong> Participate in process and technology improvement initiatives and ensure strict compliance with all procedures and regulations.</p></li></ul><p><strong>This may be the right role for you if you have:</strong></p><ul><li><p>A well-developed knowledge of clinical imaging across multiple indications alongside an in-depth knowledge of multiple imaging vendors.</p></li><li><p>Excellent communication and organizational skills alongside strong capabilities to provide succinct and impactful updates that demonstrate a developed understanding of the impact of imaging.</p></li><li><p>People management experience is highly preferred as the role will be expected to mentor other team members effectively and may have direct reports. </p></li></ul><p><strong>In Order to be considered qualified for this role you must have:</strong> <strong>:</strong></p><p>· BA/BS with 8+ years of clinical trial imaging experience</p><p>· Certification as a Registered Technologist (R.T.) with experience in modalities like CT, MRI, or Nuclear Medicine is highly preferred</p><p>· At least 3 years of imaging operational clinical trial experience in a pharmaceutical (sponsor) setting </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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Grand Rapids, MI]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44988]]></requisitionid>
    <referencenumber><![CDATA[R44988]]></referencenumber>
    <apijobid><![CDATA[r44988]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44988/medical-specialist-i-dermatology-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>Geography: Grand Rapids North</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Neurology Genetic Medicines]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45208]]></requisitionid>
    <referencenumber><![CDATA[R45208]]></referencenumber>
    <apijobid><![CDATA[r45208]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45208/senior-medical-director-clinical-development-neurology-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>The Senior Medical Director, Regeneron Genetic Medicines Clinical Development Unit (RGM CDU) is a qualified physician scientist with significant pharmaceutical/biotechnology sector and exceptional academic clinical trials experience. With oversight from Executive Medical Director manager, the Senior Medical Director works with other members of the cross-functional team to deliver translational and clinical programs from target nomination to registration. </p><p>A typical day in the life may include the following responsibilities:</p><ul><li>Serves as the clinical champion for research programs from target nomination to clinical candidate selection and contributes to the evaluation of novel targets and modalities</li><li>Leads the Global Clinical Sub-Team to deliver clinical programs from development candidate selection to registration</li><li>Designs human studies, including first-in-human, proof-of-concept, and registrational studies</li><li>Leads Cross-Functional Study Teams to deliver human studies</li><li>Maintains a high-trust, collaborative environment with team members at partner biotech companies across co-development programs</li><li>Mentors and develops team members</li><li>Contributes to RGM activities by interacting with scientists across the RGM CDU, RGC, and RGM Therapeutic Functional Area, presenting project work, fostering cross-project learning, best-practice adoption, and a culture of scientific excellence</li></ul><p>This job may be for you if you have the following:</p><ul><li>M.D. degree. (MD/Ph.D. preferred) Board Certification/Eligibility in a relevant therapeutic area (Neurology, NeuroPsychiatry, Clinical Genetics) preferred</li><li>At least 4 – 8 years of clinical development pharmaceutical industry experience</li><li>Has authored and published in medical/scientific peer-reviewed journals. Interactions with Regulatory agencies or Common Technical Document (CTD or “dossier”) submission in any ICH region are an advantage</li><li> Effective communications (verbal & written) and presentation skills are essential</li><li> Must be able to work productively in a fast-paced collaborative environment</li><li>Demonstrated critical thinking skills and sound decision-making</li><li>Prior experience with mentoring and leading cross functional teams</li></ul><p>This role is based on-site in Tarrytown 4 days/week.</p><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</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>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Feb 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Staff Engineer, Data Management]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45058]]></requisitionid>
    <referencenumber><![CDATA[R45058]]></referencenumber>
    <apijobid><![CDATA[r45058]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45058/senior-staff-engineer-data-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>The Data Enablement and Analytics (DEA) team, within the PAPD (Product, Analytics and Process Development) organization, is a multi-functional team that drives PAPD’s digitalization efforts by making data usable and useful!</p><p>The Data Management Architect defines and governs the end-to-end architecture of data systems that power preclinical science and operations. You will architect domain-driven data models, curated datasets, and integration patterns across data lakes, lab systems and analytical tools, while enabling self-service visualizations. You will drive data quality, lineage, metadata and data catalog standards, and platform patterns. To accomplish this, you will partner with numerous teams and departments and deliver value through Agile approaches.</p><div></div><p><strong>A Typical Day in the Role Might Involve:</strong></p><ul><li><strong>Enterprise Data Architecture (Preclinical):</strong><br>Define data models for preclinical entities (samples, assays, lots, batches, instruments, methods), harmonized across the data ecosystem; establish golden‑record, lineage, and System or record. </li><li><strong>Data Platform Design:</strong><br>Partner with IT teams to continue our journey to a central data platform like the Research data lake or connected data marts. Partner with data engineering teams to design streaming and batch data flow (ETL vs ELT) patterns and deliver such solutions.</li><li><strong>Visualization & Semantics:</strong><br>Publish governed, analysis‑ready semantic layers and reusable data marts; define KPI/metric definitions; enable self‑service in <strong>Spotfire</strong>/<strong>Tableau</strong> with certified data sources and good performance.</li><li><strong>Data Management & Governance:</strong><br>Stand up data catalog/metadata standards, reference/master data strategies, quality controls, and lifecycle policies; partner with business data stewards in PAPD.</li><li><strong>LIMS/ELN Architecture and Solution Delivery:</strong><br>Partner with platform owners and lab teams to model experiment workflows, capture structured context at source, and ensure compliant, scalable Lab platforms like <strong>Benchling or LabWare LIMS. </strong></li><li><strong>SAFe Ways of Working:</strong><br>Act as the overall product manager and program Lead – define our roadmap and continuous delivery mechanism using Scaled Agile Frameworks.</li><li><strong>Collaboration & Change Enablement:</strong><br>Co‑create roadmaps with PAPD functional leads and department data experts; conduct design reviews; mentor engineers and citizen developers.</li></ul><div></div><p><strong>Minimum Qualifications</strong></p><ul><li><strong>Education:</strong> Bachelor’s degree in computer science, Information Systems, Bioinformatics, Biomedical Engineering, or related field.</li><li>Strong understanding of <strong>LIMS/ELN</strong> systems like <strong>Benchling</strong>, <strong>LabWare</strong> or similar <strong>is mandatory.</strong></li><li><strong>Experience:</strong> 8+ years in data architecture/engineering in a scientific or manufacturing context; proven delivery in hybrid cloud/on‑prem data lakes/warehouses.</li><li><strong>Cloud data platforms: </strong>Expertise in AWS, Snowflake, Databricks or comparable cloud data platforms and ecosystems.</li><li><strong>Database Platforms:</strong> Expertise in NoSQL, in-memory, Graph and relational databases, which form the backbone of our operations.</li><li><strong>Tooling & Platforms:</strong> Expert in <strong>data lake</strong> architectures (curation/serving layers), metadata/catalog tools, ELT/ETL data transformation frameworks;</li><li><strong>Analytics Enablement:</strong> Delivered governed, reusable datasets powering visualization tools like <strong>Spotfire</strong>, <strong>Tableau or Power BI</strong>;</li><li><strong>Ways of Working:</strong> Working knowledge of <strong>Scaled Agile (SAFe)</strong> - backlog refinement, PI planning and release management.</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Experience in <strong>preclinical/bioprocess</strong> domains (samples, assays, batches, equipment, methods).</li><li>Experience with Lab Systems for bioprocessing. </li><li>Prior work aligning data standards across R&D, QA, and Manufacturing (data integrity, traceability).</li></ul><div></div><p><strong>Core Competencies</strong></p><ul><li>Build<strong> Data Architectures</strong> that span lab, data, and analytics ecosystems.</li><li>Strong<strong> Communications </strong></li><li>Ability to <strong>Influence</strong>:</li><li>Build <strong>Roadmaps</strong>.</li><li><strong>Continuous delivery</strong> using Agile.</li></ul><div><div><div><p><br> </p></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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-New Brunswick, NJ]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45008]]></requisitionid>
    <referencenumber><![CDATA[R45008]]></referencenumber>
    <apijobid><![CDATA[r45008]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45008/medical-specialist-i-dermatology-new-brunswick-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[New Brunswick]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: New Brunswick, New Jersey (Freehold, Edison, Princeton, Neptune)</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Predictive Analytics]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45119]]></requisitionid>
    <referencenumber><![CDATA[R45119]]></referencenumber>
    <apijobid><![CDATA[r45119]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45119/senior-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>We are seeking a highly motivated and talented Senior Manager of Predictive Analytics to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop and apply predictive models 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. The candidate must have the ability to influence, with strong interpersonal skills. Excellent communication and interpersonal skills are also required as this candidate will be expected to work productively in a collaborative, team working environment.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Plan, develop, and execute large-scale analyses of proteomic and genomic datasets, with an emphasis on aging and age-related diseases.</p></li><li><p>Develop and implement methods for data harmonization and normalization across distinct cohorts to ensure consistency and reproducibility of results.</p></li><li><p>Evaluate statistical methods for disease risk prediction, and if necessary develop new methods</p></li><li><p>Turn disease prediction needs 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 research directions</p></li><li><p>Deliver clear and concise presentations of genomics and proteomic findings to leadership, ensuring alignment with organizational goals and priorities</p></li><li><p>Ability to provide data to internal, external, and non-scientific audience </p></li><li><p>Design, implement, and optimize data pipelines for high-throughput genomic and proteomic workflows, ensuring efficient processing of large-scale proteomic datasets.</p></li><li><p>Develop and integrate robust quality control (QC) measures at multiple stages of analysis pipelines to ensure data accuracy, consistency, and reproducibility.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Demonstrated expertise in statistics, machine learning and predictive analytics applied to biological data.</p></li><li><p>Demonstrated aptitude for translating research results into products or prototypes</p></li><li><p>Proven ability to independently lead and manage 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>Demonstrated ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li><p>A PhD in a relevant field (e.g., human genetics, statistics, computational biology, or related disciplines) and at least five years of experience analyzing large-scale genomics data, or a bachelors degree with at least 8 years of relevant experience.</p></li><li><p>Candidates with prior industry experience are preferred</p></li><li><p>Experience in exploratory data analysis, applied statistics, or software engineering is preferred in one or more of these domains</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 19:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology- (Toms River, NJ)]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45009]]></requisitionid>
    <referencenumber><![CDATA[R45009]]></referencenumber>
    <apijobid><![CDATA[r45009]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45009/medical-specialist-i-dermatology-toms-river-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Toms River]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Toms River, NJ (Brick, Voorhees, Cherry Hill, Barnegat, Tuckerton, Belmar)</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr Global Procurement- Lab Consumables]]></title>
    <date><![CDATA[Sun, 22 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44951]]></requisitionid>
    <referencenumber><![CDATA[R44951]]></referencenumber>
    <apijobid><![CDATA[r44951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>We are currently looking to fill a Senior Manager for the Research and Pre-Clinical Development (R&pD) Lab Consumables team. In this role you will develop and manage strategies for our subcategories, as well as planning and executing strategic sourcing initiatives. The Senior Manager will be responsible for developing sourcing specifications, requirements, and scopes of work for RFIs, RFQs, and RFPs. They will gather and assess data through benchmarking, market intelligence reports, and Voice of the Customer (VoC) interviews, and perform analytics on spend, inventory levels, utilization, and KPI measurements. We are looking for a proactive and collaborative individual who can effectively manage supplier relationships, mitigate risks, and contribute to the success and development of our team.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Being accountable for supporting the definition and implementation of the global Lab Consumables Category strategy to serve global and regional business needs as assigned.</p></li><li><p>Work closely with stakeholders to manage discussions related to the Lab Consumables Categories and aligns category priorities with Procurement management and stakeholders.</p></li><li><p>Manage negotiations, supplier management activities, and stakeholder engagement activities for the Lab Consumables Category as assigned.</p></li><li><p>Take direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Represent Global Procurement by participating in organizational decisions in the Lab Consumables categories with critical short and long-term impact on the success, efficiency, growth, and results of Global Procurement.</p></li><li><p>Demonstrate knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li></ul><p>This role may be a fit for you if you:</p><ul><li><p>Have experience successfully managing category processes, and suppliers across a breadth of categories</p></li><li><p>Can demonstrate success working effectively with cross-functional teams to drive results in the Lab Consumables category or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</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>Can support the primary relationship manager with key supplier relationship management activities.</p></li><li><p>Have knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Can leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Powerpoint)</p></li><li><p>Have working knowledge and hands on experience supporting sourcing platform technologies preferred (LabViva, Zageno, ScienceExhange, Scientist.com, others)</p></li><li><p>Ability to use data analytics, automation and visualization tools to drive insights and communicate to stakeholders and senior leadership (PowerBI, Tableau, Power Automate)</p></li><li><p>Management and implementation of inventory management programs including technology solutions (RFID, QR codes, others), consignment programs, VMI solutions, single use materials, bioreagents and media etc.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><p>Sr Manager Level: 8+ years of experience in relevant experience, functions or industries. The ideal candidate will have in-depth knowledge of managing global category processes, and suppliers.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45201]]></requisitionid>
    <referencenumber><![CDATA[R45201]]></referencenumber>
    <apijobid><![CDATA[r45201]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45201/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>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>A day in the life of a Director may look like:</strong></p><p>· Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects.</p><p>· Works independently, with guidance in only the most complex situations.</p><p>· Informs PMx management of important program and regulatory developments in a timely manner.</p><p>· Ensures analyses and documentation are of the highest quality and accuracy.</p><p>· Ensures that reports and other documents have the appropriate messaging and that a meaningful “story-line” is developed.</p><p>· Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management.</p><p>· Solves complex problems; takes a broad perspective to identify solutions.</p><p>· Has a strong publication record and actively publishes work in scientific literature</p><p>· Makes contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p><p>· Has excellent interpersonal and communication skills, both written and oral, and has ability to communicate complex information succinctly.</p><p><strong>This may be the right role for you if you:</strong></p><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><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><p>· Recognized as an expert in own area within the organization.</p><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><p>· Decisions are guided by policies, procedures and business plan; receives guidance from head of function.</p><p><strong>In order to be considered qualified for this role, </strong>you must have a PhD +8 years with a degree in Quantitative Pharmacology (pharmacometrics) or related field.</p><ul><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>A proven track record of displaying excellent interpersonal and communication skills both written and oral and ability to communicate complex information succinctly.</p></li><li><p>Proven experience developing QP elements of regulatory strategy and interacting with regulatory agencies without supervision.</p></li></ul><p>#PMx</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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Solid Tumor Oncology]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45090]]></requisitionid>
    <referencenumber><![CDATA[R45090]]></referencenumber>
    <apijobid><![CDATA[r45090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45090/medical-director-clinical-development-solid-tumor-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>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. This role may work on studies in prostate or renal cancers.</p></div><div><p><strong>As a Medical Director, a typical day may include the following:</strong></p><ul><li><p>Defines clinical trial-related goals and objectives.</p></li><li><p>Conducts literature and database research on clinical trials as needed</p></li><li><p>Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.</p></li><li><p>Leads and supervises the Clinical Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role may be for you if:</strong></p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p><br><strong>To be considered for this role</strong>, you must have a MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience. Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.</p><div><p><em>This role has a 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ.</em></p></div><div><div><div><div></div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Los Angeles South]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45817]]></requisitionid>
    <referencenumber><![CDATA[R45817]]></referencenumber>
    <apijobid><![CDATA[r45817]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45817/medical-specialist-i-allergyent-los-angeles-south/]]></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>Geography: Los Angeles South, Allergy/ENT territory</strong></p><p><strong>Key Markets include Los Angeles, Inglewood, Torrance, Long Beach and Huntington Beach </strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with <strong>a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Editor]]></title>
    <date><![CDATA[Thu, 26 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45080]]></requisitionid>
    <referencenumber><![CDATA[R45080]]></referencenumber>
    <apijobid><![CDATA[r45080]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45080/editor/]]></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>SUMMARY</strong>: The Editor will support the Head of Medical Writing Editing and more senior Medical Writing Editors by performing a full QC check of clinical regulatory documents, to ensure that they meet company standards and Health Authority guidelines. The Editor will train on more in-depth editing techniques and be expected to perform editing duties on various document types. As the individual’s editing/QC skills, knowledge of the drug development process and knowledge of regulatory document content increase, his/her responsibilities will increase. </p><p>This position is located at our Armonk, NY office and will require you to be on-site 4 days/week. We cannot offer a remote or hybrid work option.</p><p>JOB RESPONSIBILITIES:</p><ul><li>Work independently to perform high-quality QC checks of MW documents (eg, Submission Modules, CSRs, IBs)</li><li>Edit ICFs and Protocol Amendments; as knowledge and skillset improves, edit Protocols and IBs</li><li>Train on document editing and formatting for Submission Modules and CSRs</li><li>Work with more senior MWE staff to review and updates process improvement projects</li><li>Compile, verify content, and format appendices for CSRs</li><li>Ensures adherence to internal standards and procedures</li></ul><p><strong>Education</strong></p><ul><li>Bachelor’s Degree or editor of life science (ELS) certification</li></ul><p><strong>Experience</strong></p><ul><li>2 year of relevant industry experience.</li><li>Technical reading, writing and editing skills</li><li>Organizational, interpersonal and communication skills</li><li>Working knowledge of MS Word, Adobe Acrobat, PowerPoint</li><li>Be able to work independently</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>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Feb 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Allergy - Phoenix S]]></title>
    <date><![CDATA[Tue, 24 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45618]]></requisitionid>
    <referencenumber><![CDATA[R45618]]></referencenumber>
    <apijobid><![CDATA[r45618]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45618/medical-specialist-i-allergy-phoenix-s/]]></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>Phoenix S (Allergy)</strong></p><p>Key Markets include Tucson, Gilbert, Mesa, Phoenix</p><p>Our Medical Specialists are at the forefront of engaging Allergists and Immunologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p>As a Allergy Medical Specialist, a typical day might include the following:</p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Feb 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Computational Image Analysis]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45869]]></requisitionid>
    <referencenumber><![CDATA[R45869]]></referencenumber>
    <apijobid><![CDATA[r45869]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45869/principal-scientist-computational-image-analysis/]]></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 Computational Image Analysis team is seeking a motivated data scientist who is passionate about biological applications of imaging. Our team develops rigorous analytical methods for image quantification to support cutting-edge biopharmaceutical research, working collaboratively within Regeneron’s Imaging Sciences department and with diverse teams throughout the company.</p><p>We are hiring a Principal Scientist to architect high-impact, deep learning-powered image processing pipelines, deliver validated quantitative results, and contribute to data management strategy for imaging datasets of multiple modalities. Working at the intersection of science and technology, you'll build cross-functional relationships with researchers across therapeutic areas and coordinate with IT partners to enhance research capabilities.</p><p><strong>In this role, a typical day may include:</strong></p><div><ul><li><p>Defining quantitative imaging endpoints and biomarkers to meet the experimental goals of our collaborators</p></li><li><p>Leading development and validation of image processing pipelines to analyze biomedical images of various modalities, including microscopy, histology, ultrasound, PET/CT, and MRI</p></li><li><p>Executing image analysis workflows to generate quantitative results and creating advanced visualizations to facilitate interpretation</p></li><li><p>Preparing deliverables to disseminate analytical results, ensuring methods and findings are clearly communicated and documented</p></li><li><p>Playing a crucial role in data annotation and quality control to ensure the integrity and reliability of our research data</p></li><li><p>Actively participating in cross-functional meetings, including presentation of analytical plans, methods, and results</p></li><li><p>Contributing to data management efforts, guided by FAIR principles, to maintain data integrity and accelerate scientific insights </p></li></ul></div><p><strong>This role may be for you if: </strong></p><ul><li><p>You have outstanding critical thinking, attention to detail, scientific rigor, and strong analytical, problem solving, and troubleshooting skills</p></li><li><p>You have a demonstrated ability to work independently and collaboratively as part of a larger project</p></li><li><p>You are a highly effective communicator who can interface with both biologists and IT professionals to translate scientific needs into analytical endpoints</p></li><li><p>You have a positive demeanor and willingness to grow, learn, and adapt in a fast-paced research environment</p></li><li><p>You have a passion for biology, and a dedication to share, collaborate, and lift up others</p></li></ul><div><p><strong>To be considered for this role </strong>candidates must hold an advanced degree in Computer Science, Biomedical Engineering, Mathematics, or a related field (PhD with 6+ years of relevant work experience). Candidates should demonstrate the ability to understand scientific questions in the context of drug development. Proficiency in Python programming and a solid understanding of computer science fundamentals is required, including experience with version control and AI coding assistants such as Claude Code. They should possess a strong understanding of modern image processing principles, including deep learning-based approaches. Expertise in mathematics relevant to quantitative image analysis (e.g., optimization, regression, statistics, signal processing, cluster analysis, machine learning) is highly desirable. Experience developing custom analysis pipelines in an enterprise AI platform such as Dataiku and knowledge of distributed computing frameworks (e.g., PySpark) is preferred. The ideal candidate will have familiarity with a range of third-party software tools for biomedical image analysis (e.g., HALO, Imaris, 3D Slicer). Familiarity with data annotation workflows (e.g., using v7 Darwin), data management platforms (e.g., PathCore, HALO Link, Flywheel), and relevant APIs/CLIs are preferred.</p></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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, R&D Thought Leadership and Reputation]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45847]]></requisitionid>
    <referencenumber><![CDATA[R45847]]></referencenumber>
    <apijobid><![CDATA[r45847]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45847/manager-rd-thought-leadership-and-reputation/]]></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>As Manager, R&D Thought Leadership & Reputation Communications, you will play a key role in shaping and executing integrated external communications that strengthen Regeneron’s reputation, advance our scientific narrative, and position our Research & Development (R&D) senior leaders as industry authorities. You’ll translate complex science into compelling stories and orchestrate programs that engage key audiences across channels.</p><p><strong><em>This role is based at our Sleepy Hollow, NY or Tarrytown, NY location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</em></strong></p><p><strong>Why it matters:</strong></p><p>You will bridge corporate reputation and stakeholder engagement through public-facing, above-brand R&D storytelling, reputation campaigns, and executive communications across owned, earned and social channels—elevating visibility, trust and impact among key audiences.</p><p>Reporting to the Director, Research Communications—with a dotted line to the Director, Global Development Communications—this role sits within the Corporate Communications team in Corporate Affairs. You will partner closely with the Product & Pipeline Communications, Patient Advocacy and R&D teams.</p><p><strong>A typical day might include:</strong></p><ul><li><p>Supporting development of a comprehensive external communications strategy aligned to R&D and enterprise objectives, clarifying goals and audiences, key messages, and the owned, earned, social and paid channel mix.</p></li><li><p>Collaborating with scientists, physician-scientists, medical affairs, regulatory, and operational teams to translate complex scientific topics into compelling stories for use on our corporate website, social media channels, and communications campaigns.</p></li><li><p>Identifying and securing speaking engagements, media opportunities, and events for R&D functional leaders; preparing spokespeople with briefing documents and message maps; and building and maintaining relationships with trade media by proactively pitching stories and responding to inquires, as appropriate. </p></li><li><p>Leading project management and execution of reputation-building campaigns including content planning and creation, managing reviews and approvals, and ensuring on-time delivery.</p></li><li><p>Overseeing external PR agencies/vendors and external partners to drive quality, timelines, budgets, and integration across workstreams. </p></li><li><p>Defining measurement plans and dashboards using data and feedback to optimize content and demonstrate impact.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You think strategically and execute tactically to deliver measurable business outcomes.</p></li><li><p>You have exceptional writing, storytelling, and editing skills, and can translate complex scientific concepts into engaging multimedia content.</p></li><li><p>You excel at project management and can lead multiple initiatives simultaneously within a matrixed organization.</p></li><li><p>You bring strong business acumen and a creative, innovative mindset to problem-solving.</p></li><li><p>You have experience shaping executive presence and social media campaigns (LinkedIn).</p></li><li><p>You thrive in a dynamic, fast-paced and collaborative team environment. </p></li><li><p>You are proactive and agile, adaptable, and comfortable navigating ambiguity.</p></li></ul><ul><li><p>You have experience managing agencies and/or multiple vendors with strong integration skills. </p></li><li><p>You take a data-driven approach to communications planning, optimization and measurement.</p></li><li><p>You are passionate about science and relentlessly curious.</p></li></ul><p><br><strong>To be consider for this role you have:</strong></p><p>A Bachelor’s degree in a related field is required. You bring 7+ years of professional experience in strategic corporate healthcare communications, with a focus on pharmaceutical or biotech communications preferred. Agency experience preferred.</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Biostatistics - Medical Affairs]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45854]]></requisitionid>
    <referencenumber><![CDATA[R45854]]></referencenumber>
    <apijobid><![CDATA[r45854]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45854/manager-biostatistics-medical-affairs/]]></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 seeking a Manager, Biostatistics to join our team! This individual will be responsible for statistical support for oncology compounds within Medical Affairs.</p><p><strong>In this role, a typical day may include:</strong></p><p>As part of a collaborative medical affairs team, you will implement the statistical function’s role in the oncology compounds’ medical impact plans. Together with medical directors, HEOR, medical writing, market access, and other colleagues within medical affairs, you will plan and execute evidence generation efforts, such as post-hoc analysis with innovative analytical approaches, respond to payer and reimbursement needs, review investigator initiated studies, and design and execute Phase IV studies as the study biostatistician, and ensure statistical rigor in all these duties. You will also work with fellow clinical development biostatisticians and programmers to deep dive into the clinical trial data for comprehensive understanding. You will be responsible for following departmental guidelines of collaboration, innovation, and intrinsic motivation. Working in a dynamic team with a wide range of interfaces, the role requires both strategic and operational skills combining innovative statistical thinking with a strong sense of business acumen, and excellent communication and interpersonal skills. Your manager will work with you to manage stakeholders, learn about oncology and the company’s compounds, develop Regeneron cultural understanding, and general industry knowledge.</p><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Strong interest and motivation in exploring existing clinical trial data for post-hoc analysis and innovative idea investigations</p></li><li><p>Experience with clinical trial design, including observational studies</p></li><li><p>Exposure to oncology study endpoints and analysis techniques</p></li><li><p>Strong communication skills to interpret, explain, and discuss results of complex statistical concepts and analyses to both technical and non-technical audiences.</p></li><li><p>Desire to present and share results with internal and external stakeholders.</p></li><li><p>Comfort with providing scientific/statistical input into study design, formulating novel methods to problem solving, and independently developing the statistical analysis plan to implement those solutions.</p></li><li><p>Authored Statistical Analysis Plans (SAP) and Protocols</p></li><li><p>Generated tables, listings, and figures for external communication use in publications/presentations and for internal purposes.</p></li><li><p>Ability translate and apply relevant innovative statistical methodology to everyday work.</p></li><li><p>Educate and disseminate knowledge throughout the organization for areas within the expertise of medical affairs.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD / DrPH in statistics/biostatistics or related disciplines with >2 years experience in the pharmaceutical/biotech industry or MS degree in statistics/biostatistics with >7 years’ experience in the pharmaceutical industry as a statistician. </p></li><li><p>Knowledge of drug discovery/development/life cycle management(LCM) and ability to integrate statistical concepts into drug discovery/development/LCM strategies</p></li><li><p>Prior experience or knowledge of oncology is strongly preferred</p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>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>Ability to write code in at least one common statistical software is required (i.e. SAS, R, Python). Ability to read SAS code is required</p></li></ul><p>#GDBDMJobs</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Characterization Engineer 2nd Shift]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45996]]></requisitionid>
    <referencenumber><![CDATA[R45996]]></referencenumber>
    <apijobid><![CDATA[r45996]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45996/process-characterization-engineer-2nd-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>We are currently looking to fill a Process Characterization & Technology Engineer position on our Process Sciences CORE (Cross-Operational Research Extension) team with a 2nd shift, Saturday-Thursday, 6pm-2:30am schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Process Characterization & Technology Engineers are on the front line, running small scale studies in support of manufacturing operations. The cross-functional premium shift team operates in support of both upstream and downstream lab teams, generating data used to determine proven acceptable ranges for manufacturing, characterizing cell banks, executing raw material screening studies and supporting technical evaluations at small scale.<br><br>As a Process Characterization & Technology Engineer, a typical day might include the following:</p><ul><li>Performs laboratory-scale scientific investigations related to upstream biologics manufacturing process unit operations.</li><li>Conducts scaled-down production procedures to improve the efficiency and yield of candidate or existing bioprocesses.</li><li>Performs and completes small-scale development and characterization studies used to develop IPC programs for upstream and purification processes.</li><li>Performs cGLP cell banking and characterization.</li><li>Assists in the analysis of samples generated from lab scale studies.</li><li>Produces and maintains accurate records.</li><li>Maintains lab supplies and equipment.</li><li>Develops and writes protocols for small-scale studies.</li><li>Tabulates experimental results; writes process evaluation summary reports.</li><li>Presents findings at group, and possibly, at interdepartmental meetings.</li></ul><p>This role might be for you if you have:</p><ul><li>Experience with mammalian cell culture expansion using aseptic technique.</li><li>Knowledge of small-scale, fed-batch bioreactors (2L).</li><li>Lab skills in protein separation, filtration and purification.</li><li>Strong attention to detail.</li><li>Strong interpersonal, oral, and written communication skills.</li><li>Ability to operate efficiently in a fast-paced lab environment.</li><li>Ability to adapt quickly to change and be flexible.</li><li>Strong organizational skills and ability to multi-task.</li><li>Good record-keeping skills and understanding of GDP.</li></ul><p>To be considered for the Process Characterization & Technology Engineer position, you must be willing and able to work 2nd shift, Saturday-Thursday, 6pm-2:30am. You must have the following at a minimum; BS in Engineering, preferably Chemical or Biomedical Engineering, or related field or an equivalent combination of education and experience. Level is determined based on qualifications relevant to the role. <br><br>Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</p><p><br>Regeneron is an 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><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>$67,400.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44853]]></requisitionid>
    <referencenumber><![CDATA[R44853]]></referencenumber>
    <apijobid><![CDATA[r44853]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>A <strong>Manager Statistical Programming</strong> provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management.<br> </p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Develop an expertise within a therapeutic area or standard tool. Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project</li><li>Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)</li><li>Manage the effort, including esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Provide programming support for complex presentations and more complex statistical ad-hoc requests. </li><li>Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.</li><li>If applicable, lead an application development and act as the programming representative to the user audience.</li><li>Work with management to determine resource requirements for therapeutic area or department function <br>responsibilities. </li><li>Review and select resumes, screen and interview candidates for contractor and permanent positions.</li><li>Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals.</li><li>Advises all direct reports about the procedures surrounding retention of data, records, and information for <br>employees in their group.<br> </li></ul><p><strong>In order to be considered qualified for this role</strong></p><ul><li>Master’s Degree</li><li>8-10 years of relevant work experience</li><li>SAS Certification desirable.</li><li>Also acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ultra-Pure Water Technician, Saturday - Tuesday 3rd Shift]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45367]]></requisitionid>
    <referencenumber><![CDATA[R45367]]></referencenumber>
    <apijobid><![CDATA[r45367]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45367/ultra-pure-water-technician-saturday-tuesday-3rd-shift/]]></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 looking to fill an Ultra-Pure Water (Clean Utilities) Technician position with a Saturday - Tuesday 10:00pm-8:30am shift. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Clean Utilities Technicians support the manufacturing process through involvement with start-up, operation, monitoring, maintaining and shutdown of clean utility systems and equipment within Clean Utility mechanical rooms.</p><div><div><div><div><p><strong>Please note training will be Monday-Friday 7:00am-3:30pm for the first few months. Working hours thereafter will be Saturday - Tuesday 10:00pm-8:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p><strong>As a Clean Utilities Technician, a typical day might include the following:</strong></p><ul><li>Performing preventative and predictive maintenance on related clean utilities and systems that support manufacturing.</li><li>Maintaining water rooms and related equipment such as pumps, motors, Water for Injection (WFI) stills, Clean Steam Generators and related piping.</li><li>Performing activities such as troubleshooting, hands on repairs on all related clean utility equipment and systems, and WFI point of use flushing.</li><li>Maintaining documents and records on all validated equipment and systems.</li><li>Collaborating with other departments and contractors on scheduling repairs and maintenance of clean utility systems.</li><li>Perform monitoring and control of systems utilizing computer driven Building Automation System (BAS) and PLC controls</li><li>Communicating with management regarding change documentation as necessary.</li><li>Following current Good Manufacturing Practices (cGMPs) and Good Business Practices (G).</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur.</li><li>Participating in rotational on-call schedule.</li></ul><h3>This role might be for you if you:</h3><ul><li><p>Can read and/or understand piping, electrical, and instrumentation drawings</p></li><li><p>Possess basic troubleshooting skills as they relate to the water room and mechanical aptitude</p></li><li><p>Demonstrate basic problem solving skills</p></li><li><p>Understand additional mechanical equipment and systems such as pharmaceutical compressed air, domestic water lines, plant steam and high/low pressure condensate return systems</p></li><li><p>Can learn and follow routine procedures independently as well as part of a team</p></li><li><p>Have the comfort and flexibility to work in a changing environment</p></li><li><p>Are capable of lifting, pushing, and/or pulling at least 50lbs</p></li><li><p>Have basic knowledge of Microsoft Office Suite</p></li></ul><p>To be considered for the Clean Utilities Technician position you must be willing and able to work Saturday - Tuesday 10:00pm-8:30am. Applicants must meet the education and experience minimums listed below for each level: </p><ul><li>Clean Utilities Technician I: HSD/GED with 2+ years of related experience OR AAS degree and 0+ years</li><li>Clean Utilities Technician II: HSD/GED with 5+ years of related experience OR AAS degree and 2+ years of related experience</li><li>Clean Utilities Technician III: HSD/GED with 8+ years of related experience OR AAS degree and 5+ years of related experience</li></ul><p>Prior experience in the maintenance and operation of large scale utilities plant is preferred but not required.</p><p>Level will be determined based on qualifications relevant to the role.</p><p>#REGENTOSK</p></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 (hourly)</strong></strong></p>$21.49 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 11:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Data Management]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44601]]></requisitionid>
    <referencenumber><![CDATA[R44601]]></referencenumber>
    <apijobid><![CDATA[r44601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44601/associate-director-external-data-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>The Associate Director, External Data Services, plays a critical leadership role, overseeing team members to ensure all activities align with Regeneron’s procedures and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver structured external data in compliance with Regeneron SOPs. The role also involves coaching, mentoring, and managing the performance of direct reports, while contributing to the department's strategic direction. Additionally, the AD works with senior leadership to define goals, staffing needs, and departmental structure.</div><div><div><div><div><p><strong>A typical day in the life as an Associate Director, External Data Services includes: </strong></p><ul><li><p>Shape and implement the strategy for External Data Services.</p></li><li><p>Lead and manage a team of External Data Services Managers and Specialists.</p></li><li><p>Oversee the development and maintenance of all DTS documents, ensuring alignment with Regeneron standards, processes, and timelines.</p></li><li><p>Drive the External Data Vendor Oversight model, establishing effective communication, partnership-level processes, and portfolio-level transparency on DTS status and escalations.</p></li><li><p>Represent External Data Services in leadership forums and technology discussions.</p></li><li><p>Contribute to and execute the External Data Services technology strategy.</p></li><li><p>Provide expert-level guidance to CROs, stakeholders, and external vendors on External Data Services.</p></li><li><p>Identify process gaps and lead initiatives to improve processes.</p></li><li><p>Track milestones and deliverables, escalate issues, and communicate portfolio-level updates to stakeholders.</p></li><li><p>Lead or contribute to special projects requiring strategic input and expertise in External Data.</p></li><li><p>Serve as a subject matter expert (SME) for complex topics requiring leadership-level commitment.</p></li><li><p>Develop SOPs, Work Instructions, Guidance Manuals, and other DTS development tools.</p></li><li><p>Provide coaching, mentoring, and performance management for direct reports.</p></li><li><p>Manage resource allocation and planning for External Data Services.</p></li></ul><p><strong>This Role Might Be for You If You:</strong></p><ul><li><p>Have expert knowledge of regulations like 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards for data collection.</p></li><li><p>Possess deep expertise in Data Management, External Data processes, and industry best practices.</p></li><li><p>Demonstrate advanced experience with extracting data in SAS, CSV, and XML formats.</p></li><li><p>Can address complex External Data challenges and recommend actionable solutions.</p></li><li><p>Have a proven ability to develop best practices and processes to achieve objectives.</p></li><li><p>Exhibit strong problem-solving, analytical, and project management skills.</p></li><li><p>Thrive in a matrix environment with virtual teams and can motivate others effectively.</p></li><li><p>Possess an excellent understanding of cross-functional activities and their intersections with External Data.</p></li><li><p>Manage multiple priorities with attention to detail and deliver results within tight timelines.</p></li><li><p>Communicate effectively through strong interpersonal, oral, and written skills.</p></li><li><p>Adapt quickly in a fast-paced, dynamic environment.</p></li><li><p>Are open to travel up to 20%.</p></li></ul><p><strong>To be qualified for this role, you must meet the following requirements:</strong></p><ul><li><p>A minimum of <strong>10+ years of experience</strong> in External Clinical Data Management, with expert knowledge of database structures in biotechnology, pharmaceutical, or health-related industries.</p></li><li><p>At least <strong>4 years of people management experience</strong>.</p></li><li><p>A <strong>Bachelor’s degree</strong> in Science, Health, Computing, or a related field.</p></li><li><p>Hands-on experience with <strong>Imaging Data</strong> is required.</p></li><li><p>Advanced knowledge of <strong>Biomarker data types</strong> and/or Imaging Data for oncology and non-oncology studies is a plus.</p></li><li><p>Expert knowledge of database structures is preferred.</p></li></ul><p>This role is ideal for a seasoned professional who thrives at the intersection of leadership, technical expertise, and strategic vision. If you’re ready to make a significant impact in External Data Services, this position could be your next career milestone.</p></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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 11:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, People Analytics & Insights]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45959]]></requisitionid>
    <referencenumber><![CDATA[R45959]]></referencenumber>
    <apijobid><![CDATA[r45959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45959/manager-people-analytics-insights/]]></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 Manager, People Analytics & Insights will partner with colleagues from across human resources and internal customers to provide evidence-based insights on the people and organizational aspects of Regeneron’s business. The ideal candidate will have a fundamental technical background, strong project management skills, customer orientation and requisite HR experience. Expertise in data management, metrics and reporting, descriptive and predictive analytics, data visualization and storytelling are all critical for success in this role. We see this as a phenomenal opportunity to build people analytics expertise working closely with others who have been shaping an enterprise-wide people analytics program.</p><p><strong><em>This role could be based at our Sleepy Hollow, NY, Rensselaer, NY, or Warren, NJ location with a minimum of 4 days onsite required - this is not open to fully remote or hybrid work.</em></strong></p><p>As the Manager, People Analytics & Insights, a typical day might include the following:</p><ul><li>Building datasets and conducting custom analytics projects, spanning descriptive and predictive analytics</li><li>Leading open-ended text analysis to summarize survey comments and establish foundational AI capability</li><li>Supporting ongoing reporting for select leadership audiences, including opportunities for automation and efficiency</li><li>Translating metric priorities into new dashboards in Workday and key reports with compelling visualizations and storytelling to help guide decision-making regarding Regeneron’s talent and organizational practices</li><li>Identifying, prioritizing and implementing improved data quality and additional data capture opportunities in partnership with HR Technology, IT and Finance teams</li><li>Working closely with colleagues to build and integrate people data and HR analytical capability</li></ul><p>This job might be for you if:</p><ul><li>You have high attention to detail and can easily shift gears between ongoing work and ad hoc requests</li><li>You have the ability to balance multiple projects, while informing key partners of progress and outcomes</li><li>You can handle ambiguity and are highly adaptable and flexible to changing requirements and business demands</li><li>You are adept with large and complex datasets to answer business questions</li></ul><ul><li>You possess the demonstrated ability to tell a story through data and communicate effectively with key partners through advanced visualization techniques</li></ul><ul><li>You have learning agility and a desire to keep up with the latest developments in the field of HR reporting, analytics and related technology</li></ul><p>To be considered for this opportunity, you must have a minimum of an Advanced Degree (Masters, PhD) in an applied social science or quantitative field. Preferably with 7+ years of experience (for PhD, 3+ years) working with HR, People and Business data to generate critical insights for leaders and decision makers (including working with big data, integrated business data, global data, labor market data and third-party data). This includes expertise in managing data collection, organization and quality assurance for the purposes of building statistical models, leading metrics and sustainable reporting.</p><p>We need someone who is experienced in building supervised and unsupervised machine learning models, including understanding of use cases for alternative modeling methodologies. Advanced proficiency in statistical software packages (e.g., R, Python, SAS, SPSS) and data visualization tools (e.g., Tableau, Qlik) is required. Experience with global HR technology systems and human capital platforms (e.g., Workday) is also required. We would love to find someone with both quantitative and qualitative research, design and analysis experience, including natural language processing and sentiment analysis.</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development Quality Lead Japan (GDQL-J)]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45173]]></requisitionid>
    <referencenumber><![CDATA[R45173]]></referencenumber>
    <apijobid><![CDATA[r45173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45173/senior-manager-global-development-quality-lead-japan-gdql-j/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a passionate and experienced Senior Manager to join our Global Development Quality & Regulatory Compliance team as the Global Development Quality Lead for Japan (GDQL-J). In this key role, you will lead quality and compliance initiatives within our local affiliate operations, supporting GCP, GVP, Medical, and Regulatory Affairs. This position offers an exciting opportunity to create strategic partnerships, drive proactive, risk-based quality activities, and foster a culture of continuous improvement. If you are ready to make a meaningful impact and grow with us, we encourage you to apply.</p><p><strong>A Typical Day:</strong><br>In this dynamic role, you will:</p><ul><li>Lead GVP-compliant quality activities in collaboration with the business and GDQM team.</li><li>Provide expert guidance on inspection readiness, preparation, and management at the local affiliate level.</li><li>Partner with cross-functional teams to implement and sustain quality processes.</li><li>Conduct audits and support issue management related to GVP, GCP, Regulatory, and Medical Affairs.</li><li>Mentor, coach, and manage junior team members, fostering their professional growth.</li><li>Collaborate with local and global stakeholders to align quality strategies and operations.</li><li>Act as a subject matter expert in GCP and GVP, providing training and consultations.</li><li>Drive process improvement initiatives to enhance efficiency and compliance.</li></ul><p><strong>This Role May Be For You If:</strong><br>You are someone who:</p><ul><li>Thrives in a collaborative environment and builds strong stakeholder relationships.</li><li>Has a proactive approach to quality management and risk assessment.</li><li>Excels in managing complex quality issues and compliance activities.</li><li>Enjoys mentoring and developing team members to achieve their full potential.</li><li>Is detail-oriented and committed to maintaining the highest standards of quality.</li><li>Values innovation and continuous learning to stay ahead in the pharmaceutical industry.</li><li>Communicates effectively and influences peers and senior leaders alike.</li><li>Is adept at managing multiple priorities and delivering results under tight deadlines.</li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor’s degree and at least 8 years of relevant experience in the healthcare or pharmaceutical industry, with a strong background in quality management or clinical development. Advanced knowledge of GCP and GVP guidelines, along with experience in regulatory inspection management, is essential. Preferred qualifications include expertise in risk-based quality management and proficiency in Microsoft Office tools. Native level Japanese proficiency and business level English proficiency is required.</p><p>This is your chance to be part of a team that values integrity, innovation, and excellence. Join us in shaping the future of quality and compliance in the pharmaceutical industry. Apply today!</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Utilities Technician, Saturday - Wednesday Shift]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45762]]></requisitionid>
    <referencenumber><![CDATA[R45762]]></referencenumber>
    <apijobid><![CDATA[r45762]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45762/utilities-technician-saturday-wednesday-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>We are currently looking to add a Utilities Technician to our growing team with a Saturday - Wednesday 10:00pm-8:30am shift. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Utility Technicians are responsible for operations and maintenance of High Purity Water/Steam systems and Plant Utility systems that support that manufacturing process. This is a diverse maintenance position with growth potential in a growing company.</p><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for the first few weeks. Working hours thereafter will be Saturday - Wednesday 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>As a Utilities Technician, a typical day might include the following:</strong></p><ul><li>Maintaining water room and boiler room related equipment, including pumps, motors, clean and plant utilities pre-treatment systems, Water for Injection (WFI) stills, Clean Steam Generators, high pressure steam, plant steam boilers, boiler controls, condensate return, natural gas, domestic potable water, tepid water, wastewater, and related piping</li><li>Performing activities such as troubleshooting and hands on repairs on Clean Utility and Plant Utility equipment and systems</li><li>Following current good manufacturing practices (cGMPs)</li><li>Participating in rotational on-call schedule for site emergency work</li></ul><h3><strong>This role might be for you if you:</strong></h3><ul><li>Are adept at reading and/or understanding piping, electrical, and instrumentation drawings</li><li>Possess basic troubleshooting skills and mechanical aptitude as related to the utilities being maintained</li><li>Are capable of lifting, pushing, and/or pulling at least 50lbs</li><li>Are comfortable and flexible working in a changing environment</li><li>Can learn and follow routine procedures</li></ul><p>To be considered for the Utilities Technician position you must be willing and able to work Saturday - Wednesday 10:00pm-8:30am. Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies subject area and the following minimum amounts of relevant experience for each level, preferably in a cGMP environment:</p><ul><li>Utilities Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Utilities Technician III: 5+ 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>#REGENTOSK</p><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 (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor, Quality Assurance (Shop Floor)]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45631]]></requisitionid>
    <referencenumber><![CDATA[R45631]]></referencenumber>
    <apijobid><![CDATA[r45631]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45631/supervisor-quality-assurance-shop-floor/]]></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>Regeneron is currently looking for a Sr Quality Assurance Specialist (Supervisor) position. This position performs and leads activities “on the floor” in support of dispositioning product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.</div><div><div><p>Work Schedules:</p><ul><li><p>Wednesday-Saturday, 1st shift, 6am-4:30pm</p></li></ul><p>In this role, a typical day might include the following:</p><ul><li><p>Represent Quality Assurance in support of complex and/or significant Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</p></li><li><p>Represents the organization on behalf of QA with external partners to communicate QA policy and procedures; liaise with external partners and provide input on regulatory communication</p></li><li><p>Train and/or mentor employees, including providing insights and education on processes and procedures, and conveying expectations of QA organization</p></li><li><p>Provides consultation or advice in alignment with QA policies through a continuous on the floor presence, working with stakeholders by providing QA guidance to events or questions that may arise</p></li><li><p>Perform activities associated with disposition of product (e.g., manufacturing record review, document review, source data review etc.). </p></li><li><p>Review, edit, or approve Regeneron controlled documents</p></li><li><p>Review and approve investigations associated with product or processes</p></li><li><p>Continually evaluating Regeneron processes and procedures with an eye toward continuous improvement</p></li><li><p>Supervising direct reports</p></li><li><p>Participates with employee training to ensure that all requirements are met.</p></li><li><p>Performs, minimally, monthly performance feedback meetings with direct reports.</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have an understanding of biologics manufacturing operations</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li><li><p>Are able to stand for periods of time when performing tasks on the floor</p></li></ul><p>Gowning and Environment:</p><ul><li><p>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>To be considered for this role you must hold a Bachelor’s degree and 6+ years of relevant experience. May substitute proven experience for education requirement.</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 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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Facilities Maintenance Technician, 2nd shift Monday-Friday]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45254]]></requisitionid>
    <referencenumber><![CDATA[R45254]]></referencenumber>
    <apijobid><![CDATA[r45254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45254/facilities-maintenance-technician-2nd-shift-monday-friday/]]></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 looking for a Facilities Maintenance Technician to join our team based at our <strong>Menands, NY</strong> location. This role involves hands-on maintenance, solving, and repair of facilities systems and equipment to support the manufacturing of life-changing biopharmaceuticals. Initial training will take place at our Rensselaer site, with work locations varying across sites in Rensselaer and Menands, NY, as needed.</p><p><strong>Please note training will take place Monday-Friday 1st shift 8:00am-4:30pm for approximately 2 months. Working hours thereafter will be 2nd shift Monday-Friday 2:00pm-10:30pm.</strong></p><p>As a Facilities Maintenance Technician, a typical day might include:</p><ul><li><p>Performing preventative maintenance (PMs) and work orders (WOs) on HVAC systems, chilled water systems, air compressors, and other facilities equipment.</p></li><li><p>Troubleshooting and repairing industrial HVAC systems, air handler units, and utility systems.</p></li><li><p>Assisting with utility operations, including boilers, water systems, compressed gases, and cleanroom maintenance.</p></li><li><p>Monitoring and responding to alarms from Building Automation Systems (BAS) or Programmable Logic Controls (PLC).</p></li><li><p>Supporting pest control, inspection readiness, and general building maintenance tasks.</p></li><li><p>Coordinating and supervising contracted maintenance services.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have a solid understanding of industrial HVAC systems and can read piping, electrical, and instrumentation drawings.</p></li><li><p>Enjoy working across a range of systems in a cGMP environment.</p></li><li><p>Are committed to safety and quality standards.</p></li><li><p>Are flexible, thorough, and comfortable working in a dynamic environment.</p></li><li><p>Can lift, push, and pull up to 50 lbs and have basic computer skills (e.g., Microsoft Office).</p></li></ul><p>To be considered for the Facilities Maintenance Technician position you must be willing and able to work Monday-Friday 2:00pm-10:30pm. You ideally should have an AAS degree in Engineering, Construction Technologies, or a related field (preferred) and the following minimum years of experience for each level:</p><ul><li><p>Facilities Maintenance Technician II: 2+ years of related experience or HSD/GED with 8+ years of experience</p></li><li><p>Facilities Maintenance Technician III: 5+ years of related experience or HSD/GED with 8+ years of experience</p></li><li><p>Facilities Maintenance Technician IV: 8+ years of related experience or HSD/GED with 10+ years of experience</p></li></ul><p>Prior experience with large-scale utilities plants is preferred.</p><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 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 (hourly)</strong></strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Business Operations Specialist]]></title>
    <date><![CDATA[Sat, 14 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45598]]></requisitionid>
    <referencenumber><![CDATA[R45598]]></referencenumber>
    <apijobid><![CDATA[r45598]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45598/senior-it-business-operations-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>Within this role you will be a vital part of the IOPS IT Business Operations function supporting core business services such as Procurement Management, Financial Management, License Management & Process Improvement.</p><p>As a Senior IT Business Operations Specialist, a typical day might include, but is not limited to, the following:</p><ul><li>Coordinating & Supporting Procurement activities for IOPS IT in collaboration with our IT user base</li><li>Building partnerships with SS&P to ensure alignment with their procedures and adhering to spending controls</li><li>Maintaining appropriate financial data to allow for data driven insights and analysis</li><li>Providing support to the Budget and Forecasting Planning cycles</li><li>Working with developers on our financial reports to ensure data is accurate and available</li><li>Maintaining the License Management database to ensure on-time renewals occur</li><li>Contributing to reports on IT Business Management progress to​ procurement, contractor management, project managers, and/or operations​ teams as necessary</li><li>Implementing and maintaining processes and documentation to support efficiencies within the group</li><li>Supporting the IT Business Operations Manager as required in continuous improvement initiatives.</li></ul><p>This role might be for you if you:</p><ul><li>Have broad experience in administering business practices to create the highest level of efficiency</li><li>Have steered purchasing procedures and activities</li><li>Have in-depth experience with financial management practices</li><li>Are proficient in using asset management applications</li><li>Have experience with developing and maintaining business processes and suggest improvements</li><li>Have demonstrated experience of working on your own initiative and having work across diverse and global teams</li><li>Are detail oriented and focused on maintaining data to a high standard & accuracy.</li></ul><p>To be considered for this opportunity you should have a BA/BS in Business, Financial, Management, or related field and 5+ years of Business Operations experience.</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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 15 Mar 2026 08:56:37 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists  - Hematology-Charlotte, NC]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46211]]></requisitionid>
    <referencenumber><![CDATA[R46211]]></referencenumber>
    <apijobid><![CDATA[r46211]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46211/medical-account-specialists-hematology-charlotte-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Charlotte]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Hematology Oncology Account Specialist, is responsible for engaging Hematologist/Oncologists 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 Hematology 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 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 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><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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45803]]></requisitionid>
    <referencenumber><![CDATA[R45803]]></referencenumber>
    <apijobid><![CDATA[r45803]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>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><strong>In this role, a typical day might include:</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></ul><p><strong>This role might be for you if can/have:</strong></p><ul><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>To be considered for this opportunity, you must have the following:</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><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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Training, Market Access & Reimbursement (Neurology)]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46252]]></requisitionid>
    <referencenumber><![CDATA[R46252]]></referencenumber>
    <apijobid><![CDATA[r46252]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46252/senior-manager-commercial-training-market-access-reimbursement-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Commercial Training, Market Access & Reimbursement is responsible for developing, delivering and coordinating training materials for market access, specialty pharmacy, patient support and access programs and reimbursement-specific teams. Focus areas include product launch and competitive readiness training, market access, customer interaction skills, and national field meeting preparation including workshop development for the Neurology field reimbursement teams.</p><p>Additional areas of responsibility may include logistical support and coordination of the training of Neurology colleagues, as needed, in international markets. Training support includes all areas of commercialization for the Neurology business unit including sales, marketing, and reimbursement. This position reports to the Director, Commercial Training, Neurology.</p><br><h3><strong>A typical day may include the following:</strong></h3><p><em>Develop</em></p><ul><li>Design and development of product training for pre-launch, post-launch, POA and advanced training including conducting needs assessment with relevant collaborators</li><li>Creates and facilitates workshops for launch, POA and other training meetings, using best-in-class means of training delivery including eLearning, self-study, computer-based training, audio/video, classroom, and experiential learning to ensure the relevant teams are trained to effectively and compliantly deliver the access and acquisition related attributes of our products and services</li><li>Develops content for and facilitates new hire, Phase II, and advanced training</li><li>Responsible for developing training activities, including backgrounders and FAQs on payer landscape and pull-through associated with promoting and driving brand strategies and tactics</li></ul><p><em>Operate</em></p><ul><li>Collaborates and aligns with field force effectiveness, medical, commercial operations, market access, and brand marketing to develop and deliver high-impact training</li><li>Provides courses that will engage and motivate attendees, using a variety of media</li><li>Assists in the development of Regeneron Field Trainers</li><li>Partner with commercial leadership and department of Learning and Leadership Development to determine performance models and identify gaps in order to provide recommendations on appropriate representative, market access and management training to enhance performance and business results</li><li>Monitors the effectiveness of training programs through testing and metrics platforms, employing data to enhance the development and execution of Neurology market access training</li></ul><p><em>Execute</em></p><ul><li>Ensures all training is provided in accordance with company policies and procedures and is conducted in strict compliance with all applicable laws and regulations</li><li>Ensure the field force is educated and effectively trained to align with all legal and regulatory requirements, including HIPPA, PhRMA Code, OIG Compliance, PDMA, etc. This requires coordination of key internal functions for training materials and workshop development as well as certification of sales and other commercial personnel</li><li>Ensures all developed materials are appropriately approved through the Medical/Legal/Regulatory process.</li><li>Remains abreast of the industry, life sciences, and training related topics. Maintain familiarity with the Neurology space and competitive products.</li><li>Conducts field visits with Field Reimbursement Managers to keep abreast of current trends and identify training opportunities</li></ul><h3><strong>This May Be the Right Role for You If you:</strong></h3><ul><li>You have success in Access & Reimbursement, Reimbursement Leadership, Commercial or Reimbursement Training & Development</li><li>You bring strong communication skills, ability to work across multiple departments and create effective teams</li><li>You can manage multiple priorities, with strong organizational, planning, and project management skills are necessary</li><li>You have mastery in presentation, facilitation, collaboration and influencing skills are required</li></ul><p>To be considered, we are expecting you to have a Bachelor’s degree required and 8+ years of progressive experience within the pharmaceutical/ biotech industry. With at least 2 years formal training or regional training experience preferred. You bring product launch, buy & bill, and infusion experience as well. We are hopeful you have experience in the Neurology space. This is a remote role with frequent travel.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 14:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Digital Health Technologies  (eCOA)]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44631]]></requisitionid>
    <referencenumber><![CDATA[R44631]]></referencenumber>
    <apijobid><![CDATA[r44631]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44631/senior-manager-digital-health-technologies-ecoa/]]></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>As a Senior Manager, Digital Health Technologies (DHT) you will be accountable for implementation of digital tools and technologies (e.g. electronic COA (eCOA), eConsent, wearables, sensors, spirometry, ECG) in individual clinical research studies from study design to close out. We support digital tool and technology project timelines, translation, specifications, implementing UAT, and ensuring collection of such data in accordance with our SOPs and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs). </p><p>This position is on-site either in Sleepy Hollow, NY or Warren, NJ locations. If eligible, we can offer relocation assistance. We cannot offer a remote work option. </p><p><strong>A typical day may include the following:</strong> <br>• Responsible for reviewing and approving various project related digital tool and technology study documentation during the course of the project lifecycle.<br>• Applies patient technology expertise on day-to-day activities when issues are brought up.<br>• Communicates with internal and external partners and raises risks.<br>• Provides input into protocol development as it relates to digital tools and technologies.<br>• Support the integration of all supported digital tools and technologies into existing systems and workflows to minimize disruption and improve efficiency. <br>• Oversee or supports license acquisitions and purchasing of digital tools and technologies.<br>• Responsible for the selection of the digital tool and technology vendor selection, in collaboration with study team.<br>• Oversee vendor performance at the clinical trial level, performing root cause analysis and identifying corrective actions, and serving as point of escalation for issues. <br>• Project plan development, execution, and change control. Coordinates resolution & risk mitigation of all supported technology systems related issues and end of study vendor deliverables <br>• Provides support for problem resolution between vendors and Regeneron study team. <br>• Monitor financial components related to digital tools and technologies for each study. <br>• Collaborate with study team members on medical monitoring plan. <br>• Collaborate with data management on all digital tool data specifications, standards, and transfers. <br>• Provides training and mentor new staff.<br>• Apply problem solving strategies to issues and maintain issue tracking documentation to monitor progress and ensure timely resolution to escalations.<br>• Develop strategy & processes for expansion of eSource modalities to enable data availability in a virtual clinical trial environment.<br>• Communicates clinical innovations in eSource modalities to stakeholders and broader organization.<br>• Develop trial strategy for implementation of innovative clinical trial technologies and radical innovations.<br>• Provide consultation on all digital tool modality benefits, risks, costs and process.<br>• Facilitates and contributes to study level lessons learned.<br>• Recommends and participates in cross-functional and departmental process improvement initiatives.<br>• May require up to 25% travel.</p><p><strong>This may be for you if you: </strong><br>• Want to have an impact on patient lives.<br>• Have a data driven approach to planning, executing, and problem solving<br>• Can demonstrate effective project management skills, cross-functional team leadership and organizational skills.</p><p>To be considered you are to have a bachelor’s degree and minimum of 8+ years’ relevant industry experience. Demonstrate knowledge of digital tools and technologies within the eCOA systems development processes. Ability to understand and implement our strategic direction and guidance for respective clinical studies. Technical proficiency in trial management systems and Microsoft Project Server. Knowledge of ICH/GCP and regulatory guidelines/directives<br> </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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Research Informatics]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45670]]></requisitionid>
    <referencenumber><![CDATA[R45670]]></referencenumber>
    <apijobid><![CDATA[r45670]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45670/manager-clinical-research-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[<div><p>The Regeneron Genetics Center uses data on millions of people to understand human disease and guide Regeneron’s therapeutic programs. Essential to these efforts is our ability to organize and interpret the health history of each individual we study. In our Clinical Informatics and Data Science team, you will join a talented team of individuals and play a central role in our research efforts across diverse therapeutic areas – ranging from cancer, to immunology, to neuroscience.</p><p>You will help us to organize, analyze and interpret health information aggregated from health records, surveys, and digital devices across multiple collaborators. You will participate in designing data and software solutions, use cutting edge cloud infrastructure and data engineering tools, and interact with Regeneron scientists and leaders. This will be a dynamic, challenging position with lots of work and lots of opportunities for learning and advancement.</p><p><strong>As a Manager Clinical Research Informatics, a typical day might include</strong>:</p><ul><li><p>Developing and maintaining software tools and building blocks that allow Regeneron scientists to understand, interpret, and interact with health data. Familiarity with Python and/or C++ is expected.</p></li><li><p>Automating the processing, QC and harmonization of electronic health records, surveys, and other data for thousands of individuals. Familiarity with Python’s data science libraries such as pandas, Polars, scikit, TensorFlow and pyTorch will be extremely handy.</p></li><li><p>Discussing the challenges, opportunities and pitfalls of using health data to understand human disease and biology and guiding Regeneron scientists as they use health data to truly understand human disease. You will need an understanding of epidemiology and data analysis principles.</p></li><li><p>Working with modern cloud environments and platforms. A knowledge of Amazon Web Services and related toolkits will be useful, but we can help you learn.</p></li><li><p>Presenting results and summaries of health datasets, data processing and data analysis plans to a variety of technical audiences, ranging from experts in statistics, epidemiology, genetics, and computation to experts in biology, drug design, and medicine. You will need outstanding communication skills!</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>A demonstrated knowledge of Python and key data science libraries is a must. Knowledge of R, SQL and/or C/C++ is also highly valued. If you have contributed to code in GitHub or another public repository, let us know.</p></li><li><p>Understanding strategies for working with structured health data and related ontologies.</p></li><li><p>Experience with data quality control, summarization and visualization.</p></li><li><p>A passion for learning. We are a fast-moving team in a fast-moving company. You should expect to encounter challenging work and to learn many new skills.</p></li></ul><p><strong>To be considered for this position </strong>you should have a PhD (or a MS/BS degree with demonstrated relevant experience) in Computer Science, Health Informatics, Clinical Informatics, Biostatistics, or a related field with at least 3 years of relevant experience organizing large datasets in a research setting, whether in academia or industry.</p></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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist Global Procurement - Buyer]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45919]]></requisitionid>
    <referencenumber><![CDATA[R45919]]></referencenumber>
    <apijobid><![CDATA[r45919]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45919/specialist-global-procurement-buyer/]]></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>We are currently looking to fill a Buyer role works within our Global Procurement organization and will be part of a team of professionals focused on the requisitions of goods, supplies and services within a specific scope and/or category of spend. The position provides daily support to Regeneron employees and suppliers and applies company purchasing policies and procedure.</p><h3>As a Buyer a typical day may include:</h3><ul><li><p>Manage daily order requests submitted by internal clients in support of their functions. Orders will be reviewed, disseminated and placed in a timely manner to meet end user needs. This will include requesting supplier quotes, issuing and approving orders in the Oracle database, reviewing requisitions for completeness and accuracy inclusive of all documentation, such as competitive bids or exception forms. Ensure proper tax exemption certificates are completed and provided to suppliers, as applicable.</p></li><li><p>Partners with internal departments to accomplish procurement-specific projects/tasks; starts to build effective relationships with internal and external customers/vendors/suppliers</p></li><li><p>Executes work under general direct supervision such as purchasing materials, scientific equipment, services, and office/business supplies. Uses requisition authorizations, engineering and production schedules to maintain inventory at planned levels.</p></li><li><p>Issues and monitors Blanket Purchase Orders and conducts scheduled reviews of activity. Communicates to end users regarding status of funds, as required.</p></li><li><p>Assist in coordinating purchasing activities with other departments to maintain inventory at planned levels.</p></li><li><p>Reconcile P-card orders in Concur monthly</p></li><li><p>Executes procurement-related projects and tasks based on specific instructions and with limited discretion</p></li><li><p>Support Audits, Compliance & Investigations, as required</p></li></ul><br><h3>This might be a good fit if you have:</h3><ul><li><p>Command of daily transactional issues and problem resolution using excellent organizational and communication skills with internal clients and suppliers</p></li><li><p>Ability to exercise sound judgment within defined procedures and practices to support Procurement Operations as required, including workload balancing during increased volume periods, working with other Procurement staff on special projects, generating reports, and performing office duties as assigned, including site specific requirements, committees, SCC walks, etc.</p></li><li><p>Experience with invoice resolution, to ensure timely and accurate closure of outstanding invoices and escalation of any issues that are not resolved in a timely manner.</p></li><li><p>Ability to create collaborative working relationships with suppliers and internal customers and train them on proper iPro requisition and PO issuance procedures to conform with established policies and procedures.</p></li></ul><p>To be considered for this role you must possess a Bachelors degree in a relevant field of study plus relevant, dynamic experience in procurement. 2-4 years' experience in similar roles within purchasing, finance, AP within a Pharma/Life Sciences/Regulated industry preferred but not required.</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>$67,400.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 13:56:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Supply Operations]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46090]]></requisitionid>
    <referencenumber><![CDATA[R46090]]></referencenumber>
    <apijobid><![CDATA[r46090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46090/manager-clinical-supply-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Clinical Supply Operations is a key member of the team, responsible for leading clinical supply activities that support the development and operation of clinical supply logistics processes. Partnering with cross‑functional teams and external vendors, you will provide operational oversight, identify and implement improvements, and drive continuous optimization using data‑driven insights.</p><p><strong>A Typical Day</strong></p><ul><li><p>Coordinate Clinical Logistics Vendors in the execution of distribution; supervise performance, drive improvements, and resolve issues to meet study timelines and quality expectations.</p></li><li><p>Collaborate with cross‑functional partners (e.g., Clinical Operations, CMC, Quality, Regulatory, Finance) to develop and improve Clinical Supply operational processes that ensure timely, in‑full delivery of clinical trial materials.</p></li><li><p>Lead cross‑functional improvement initiatives to optimize operational efficiencies, streamline handoffs, and support strategic decision‑making and problem‑solving.</p></li><li><p>Represent the needs of the team in cross‑functional forums and initiatives; champion organisational change and adoption of new or improved processes and tools.</p></li><li><p>Create and lead performance metrics and dashboards to provide clarity into operational performance, trends, and opportunities; translate insights into action plans.</p></li><li><p>Act as an advisor to team members on operational tasks, process issues, projects, and initiatives; mentor and train others to achieve high‑quality results.</p></li><li><p>Maintain standardized SOPs, work instructions, playbooks, and templates; drive continuous improvement in planning processes and vendor management.</p></li><li><p>Identify and mitigate supply risks and dependencies early; propose pragmatic solutions and secure alignment on course corrections across collaborators.</p></li><li><p>Partner with digital/data and systems teams to harness IRT/RTSM, ERP/WMS, and analytics tools for planning and tracking; ensure data integrity and audit readiness.</p></li><li><p>May directly supervise staff; set priorities, coach performance, and support development.</p></li></ul><p><strong>This Role Might Be for You If You Have</strong></p><ul><li><p>Hands‑on experience leading clinical trial supply operations and distribution, including oversight of third‑party logistics providers and pack/label/ship activities.</p></li><li><p>Strong project management skills with the ability to lead multiple concurrent workstreams, deadlines, and collaborators in a matrixed environment.</p></li><li><p>Proven vendor management expertise, including service level oversight, performance management, and continuous improvement.</p></li><li><p>Excellent communication and relationship‑building skills; adept at influencing across functions and levels.</p></li><li><p>High attention to detail with creative, data‑driven problem‑solving.</p></li><li><p>Proficiency with clinical supply and data tools (e.g., IRT/RTSM, ERP, WMS) and Microsoft Excel, PowerPoint, and Word.</p></li><li><p>Familiarity with GxP/GDP requirements and best practices for clinical supply, distribution, and documentation.</p></li></ul><p><strong>To Be Considered</strong></p><p>Bachelor’s degree in supply chain, life sciences, engineering, or a related field with 6+ years of professional experience. Experience supporting global or multi‑region clinical studies is advantageous; . Fluency in English; additional languages are a plus.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Genetics Medicines, Auditory]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45891]]></requisitionid>
    <referencenumber><![CDATA[R45891]]></referencenumber>
    <apijobid><![CDATA[r45891]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45891/senior-medical-director-clinical-development-genetics-medicines-auditory/]]></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>The Senior Medical Director, Regeneron Genetic Medicines Clinical Development Unit (RGM CDU) is a qualified physician scientist with significant pharmaceutical/biotechnology sector and exceptional clinical trials experience. With oversight from Vice President manager, the Senior Medical Director works with other members of the cross-functional team to deliver translational and clinical programs from target nomination to registration. </p></div><div><p>A typical day in the life may include the following responsibilities: </p></div><div><ul><li><p>Serves as the clinical champion for research programs from target nomination to clinical candidate selection and contributes to the evaluation of novel targets and modalities </p></li></ul></div><div><ul><li><p>Leads the Global Clinical Sub-Team to deliver clinical programs from development candidate selection to registration </p></li></ul></div><div><ul><li><p>Designs human studies, including first-in-human, proof-of-concept, and registrational studies </p></li></ul></div><div><ul><li><p>Leads Cross-Functional Study Teams to deliver human studies </p></li></ul></div><div><ul><li><p>Maintains a high-trust, collaborative environment with team members at partner biotech companies across co-development programs </p></li></ul></div><div><ul><li><p>Mentors and develops team members </p></li></ul></div><div><ul><li><p>Contributes to RGM activities by interacting with scientists across the RGM Clinical Development Unit, Regeneron Genetics Center, and RGM Therapeutic Functional Area, presenting project work, fostering cross-project learning, best-practice adoption, and a culture of scientific excellence </p></li></ul></div><div><p>This job may be for you if you have the following: </p></div><div><ul><li><p>M.D. degree. (MD/Ph.D. preferred) Board Certification/Eligibility in a relevant therapeutic area (Neurology, NeuroPsychiatry, Pediatric Neurology) preferred </p></li></ul></div><div><ul><li><p>At least 4 – 8 years of clinical development pharmaceutical industry experience </p></li></ul></div><div><ul><li><p>Has authored and published in medical/scientific peer-reviewed journals. Interactions with Regulatory agencies or Common Technical Document (CTD or “dossier”) submission in any ICH region are an advantage </p></li></ul></div><div><ul><li><p> Effective communications (verbal & written) and presentation skills are essential </p></li></ul></div><div><ul><li><p> Must be able to work productively in a fast-paced collaborative environment </p></li></ul></div><div><ul><li><p>Demonstrated critical thinking skills and sound decision-making </p></li></ul></div><div><ul><li><p>Prior experience with mentoring and leading cross functional teams </p></li></ul></div><div><p>This role is based on-site in Tarrytown 4 days/week. </p></div><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</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>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Dallas E, TX]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46130]]></requisitionid>
    <referencenumber><![CDATA[R46130]]></referencenumber>
    <apijobid><![CDATA[r46130]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46130/medical-specialist-i-pulmonology-dallas-e-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[<p><strong>Geography: Dallas East (Rockwall, Tyler, Long View, Shreveport)</strong></p><p>The Medical Specialist (MS) will report to the District Manager and be responsible for engaging customers in the Pulmonary therapeutic area within an assigned geographical universe, presenting clinically focused selling messages to create and drive growth, and consistently delivering product goals.<br><br><strong>A Typical Day Might Look Like This</strong></p><ul><li><p>Demonstrate strong and consistent sales performance related to product goals 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></li><li><p>Develop strategy and execute tactics within key accounts in the Pulmonary therapeutic area to generate product utilization.</p></li><li><p>Develop strong working relationships with Pulmonologists and Midlevel experts in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p></li><li><p>Collaborate with their regional 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.</p></li><li><p>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).<br> </p></li></ul><p><strong>This Position Might Be For You If</strong><br> </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<br> </p></li></ul><p>To be considered for this role you must have a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Pulmonary market or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Market Access Strategy (Neurology)]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46291]]></requisitionid>
    <referencenumber><![CDATA[R46291]]></referencenumber>
    <apijobid><![CDATA[r46291]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46291/executive-director-market-access-strategy-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><em>This position is on-site 4 days per week and 1 day from home. A fully remote role is not possible for this position. Basking Ridge, NJ is not an option for this role.</em></p><p>The Executive Director, Market Access Strategy leads Neurology channel assessment and access strategy development, in support of the commercialization efforts of our novel siRNA C5 inhibitor being developed for Myasthenia Gravis. Focus will be on leading access initiatives in the US as well as above-brand Market Access Marketing, providing positive leadership and influence with cross-functional partners to ensure market access insights are built into brand strategies and execution. Responsibilities will also include providing strategic support and cross-functional direction to extended market access teams and external partners. This individual will report to the Senior Vice President, Global Market Access, and is expected to demonstrate independent critical thinking, and is expected to work with minimal supervision.</p><h3>In a typical day, you will:</h3><ul><li>Lead overall market access strategy for launch readiness and indication expansions. Develop strategies and tactics across channels to optimize broad access</li><li>Serve as the market access point person for brand leads. Attend all pertinent meetings, take ownership of projects/initiatives</li><li>Lead the market access launch readiness workstream to support the brand strategy, including payer landscape insights, access/channel/contracting strategy recommendations, value messaging development, and field team tactical material developments</li><li>Lead annual brand planning including market access strategy recommendations, initiative planning, and budgeting</li><li>Lead and develop payer value and communication platforms, in coordination with HEOR, marketing, medical teams, etc.</li><li>Lead the tactical material development for all field teams (as appropriate) to support the brand strategy</li><li>Develop and coordinate training efforts in support of payer facing teams</li><li>Serve as the market access point person for home office based cross-functional teams (e.g., pricing, HEOR, etc.) and all field teams, conducting regular touchpoints to discuss ongoing workstreams and future needs</li><li>Oversee tracking, initiatives and analytics around clinical pathways and guideline updates</li><li>Monitor all market access resources available for field teams and conduct reviews of current resource utilization</li><li>Developing benchmarks and metrics to assess impact of key initiatives</li><li>Managing market access budget aligned with key responsibilities</li><li>Vendor management: oversee relationship and budget with vendors pertinent to scope of work</li><li>Stay in sync with all laws, regulations and policies that govern the conduct of Regeneron activities</li></ul><br><h3>This May Be the Right Role for You If you:</h3><ul><li>You have a strong of pharmaceutical selling process, market access and pricing landscape, and state/federal policy initiatives</li><li>You can comprehend complex brand strategies and help identify market access opportunities to employ them</li><li>You can implement tactical plans while managing multiple projects simultaneously and excellent ability to prioritize work and meet deadlines.</li><li>You can work on teams and independently, multi-task and prioritize in a fast paced environment</li></ul><p>To be considered, we expect you to have a bachelor's degree at a minimum and 15+ years of industry or relevant professional experience (i.e. Physician practice, pharma consulting, patient support) and 10+ years of Market Access experience. We are seeking Rare Disease, Neurology and gMG experience.</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Administrative Coordinator]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46283]]></requisitionid>
    <referencenumber><![CDATA[R46283]]></referencenumber>
    <apijobid><![CDATA[r46283]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46283/senior-administrative-coordinator/]]></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 Administrative Coordinator is primarily responsible for managing and providing high-level administrative support to the Vice President, Neurology CBU<strong> </strong>as well as the Sales and Marketing Leads. The interim hiring manager for role this will be the Vice President of New Products.</p><p>Responsibilities include, but are not limited to, heavy calendar management, coordination of in-house and offsite meetings (sourcing, planning, execution), expense reconciliation, and arranging US and International travel. The coordinator should exercise considerable judgment and initiative with the ability to influence partners and understand key relationships, while ensuring sensitive data is held in strict confidence.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Proactively manage calendars for the VP using a thorough understanding of department and leadership priorities. Ability to anticipate the needs of leaders and teams to manage and solve problems when scheduling conflicts occur.</li><li>Arrange and coordinate heavy travel logistics for VP which may include conference registrations, travel and meeting itineraries, air, hotel, and ground transportation.</li><li>Responsible for on and offsite meeting planning, including catering, rooming lists, audio visual requests, and team builders, while ensuring adherence to budgetary guidelines.</li><li>Occasional domestic travel may be required in support of the Annual National meeting, Brand Planning meetings, and various department team builders.</li><li>Work closely with our external collaborators to coordinate meetings and events.</li><li>Demonstrates a working knowledge of company policies, procedures, resources and where to find them.</li><li>Implements a highly organized and efficient administrative workflow. Identifies, develops, and/or supports administrative process improvements.</li><li>As CBU administrative brand lead, act as a key point of contact for the department while working closely with the other administrative coordinators.</li><li>Weekly or bi-weekly touchpoints with VP and key stakeholders to review priorities and important brand activities.</li><li>Process and submit purchase requisitions and enter information into the contract management system.</li><li>Reconcile expenses for VP as well as expenses incurred for offsite meetings and department purchasing card.</li><li>Actively manage customized email distribution lists. Manage and update content on department’s SharePoint site.</li><li>Proof, edit and send email field communications on behalf of VP and Marketing Lead.</li><li>Any other ad hoc administrative assignments such as ordering birth/bereavement gifts, holiday field and inhouse gifts.</li></ul><h3><strong>This job might be for you if you have:</strong></h3><ul><li>Highly collaborative with strong written and verbal communication skills; ability to interact across all levels of employees and management while maintaining confidentiality. Ability to understand departmental and/or leader priorities and adjust work accordingly while maintaining a high level of accuracy and attention to detail.</li><li>Increased level of independence, judgment, and basic problem-solving skills. Comfortable acting as a point person for projects. Ability to work independently but also collaborate with team members.</li><li>Is a quick learner, can cope with change and ambiguity; can handle risk and uncertainty with composure and shifts gears comfortably.</li><li>Builds effective relationships up, down, and sideways. Is coachable and open to challenge and development from bosses; gains the trust and support of peers.</li><li>Proficient in MS Office, SharePoint, Concur and teleconference systems with the ability to assist with basic troubleshooting. May be responsible for training new employees on internal systems.</li></ul><p>To be considered for this role, Associates or BA preferred; 10+ years administrative experience with 2 years of (business function) industry experience desirable. Years of experience may be considered in lieu of degree.</p><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 (hourly)</strong></strong></p>$33.80 - $52.93]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Allergy-ENT - Salt Lake City N, UT]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46245]]></requisitionid>
    <referencenumber><![CDATA[R46245]]></referencenumber>
    <apijobid><![CDATA[r46245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46245/medical-specialist-i-allergy-ent-salt-lake-city-n-ut/]]></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>Geography: Salt Lake City North Allergy/ENT territory</strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p><strong>Key Markets include: </strong>Bountiful, Farmington, Idaho Falls, Logan, Layton, Ogden, Park City, Pocatello, Salt Lake City, and West Valley City.</p><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with <strong>a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Engineer, Synthetic and Bioconjugation Scale-Up Technologies (PMPD)]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44429]]></requisitionid>
    <referencenumber><![CDATA[R44429]]></referencenumber>
    <apijobid><![CDATA[r44429]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44429/staff-engineer-synthetic-and-bioconjugation-scale-up-technologies-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>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking and dynamic <strong>Staff Engineer </strong>for its Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will provide scientific leadership and support for synthetic oligonucleotide process development using the principles of Quality by Design (QbD), process scale-up, and technology transfer of manufacturing-related workflows at Contract Development and Manufacturing Organizations (CDMOs) to ensure timely and reliable entrance to the clinic through product commercialization.</p><p><strong>A Typical Day in the Role of Staff Engineer might include:</strong></p><ul><li>Designing and developing scalable, robust and controlled GMP-ready processes for chemical synthesis of small-molecules. This includes purification development and establishing supporting analytical characterization techniques.</li><li>Proactively complying to lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</li><li>Ensuring a team-based evaluation of processes by working closely with several groups such as R&D chemistry, Formulations Development, Analytical Chemistry, and Protein Biochemistry to ensure integrated program success.</li><li>Generating robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to vet CDMO’s and successfully transfer processes with immediate, first-time success.</li><li>Developing new technologies for process improvements and predictive process models, and pioneering novel at-line/in-line process analytical technologies to ensure robust processing.</li><li>Reviewing and providing domain expertise for all regulatory submissions.</li><li>Authoring publications, reports, tech transfer documents, regulatory support documents, patents.</li><li>Performing long-term planning for laboratory related personnel, supplies and equipment.</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Have strong initiative and aim to complete challenging tasks and learn new technologies.</li><li>Are capable of multi-tasking, working both independently and within a team environment.</li><li>Have excellent interpersonal, verbal and written communication skills.</li><li>Can think critically and demonstrate problem-solving skills.</li></ul><p>This role requires a Ph.D. or Master’s in organic chemistry or a related field. At least 3-6+ years of industrial experience post-PhD or a MS w/10+ years, or BS with 15+years in active pharmaceutical ingredient (API) process development is preferred. Experience with small-molecules in the bioconjugates space will be highly preferable. Hands on experience with organic molecule synthesis and characterization tools such as mass spectrometry, nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, high-performance liquid chromatography (HPLC) etc. is preferred. Candidate must be well-versed with purification techniques such as crystallization, extraction, chromatography etc. Experience with solid-phase and liquid phase peptide synthesis is preferable. Proven experience in scaling-up synthetic small-molecule reactions and technology transfer to a GMP manufacturing facility is a plus. Candidate should be well-versed with International Council for Harmonization (ICH)/regulatory guidelines and their impact on process development of synthetic</p><p><strong>A typical day in the role of Staff Engineer might include:</strong></p><ul><li>Designing and developing scalable, robust and controlled cGMP-ready processes for the chemical synthesis, purification, and isolation of oligonucleotides across early and late-stage process development.</li><li>Ensuring a team-based evaluation of processes by working closely with several groups such as R&D Chemistry, Formulations Development, Analytical Chemistry, Protein Biochemistry, CDMOs, and other key stakeholders to ensure integrated program success.</li><li>Generating robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Partnering with the External Manufacturing group and other key partners at Regeneron’s Industrial Operations and Product Supply (IOPS) organization to vet CDMOs and successfully transfer processes with immediate, first-time success.</li><li>Promote new technologies for process improvements, predictive process models, and novel at-line/in-line process analytical technologies to ensure robust processing.</li><li>Reviewing and providing domain expertise for regulatory submissions.</li><li>Authoring publications, reports, tech transfer documents, regulatory support documents, patents.</li><li>Scientifically up-to-date on advances in process chemistry and related disciplines</li><li>Requires up to 20% travel</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Have strong initiative and aim to complete challenging tasks and learn new technologies.</li><li>Are capable of multi-tasking, working both independently and within a team environment.</li><li>Have excellent interpersonal, verbal and written communication skills.</li><li>Can think critically and demonstrate problem-solving skills.</li></ul><p>This role requires a Ph.D. or Master’s in organic chemistry or a related field. At least 5 years of industrial experience post-PhD or at least 7 years of experience post-Masters in active pharmaceutical ingredient (API) process development is preferred. Experience with small-molecules in the bioconjugates space will be highly preferable. Hands-on experience with solid-phase oligonucleotide synthesis, purification, and characterization using techniques such as mass spectrometry (MS), nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, and high-performance liquid chromatography (HPLC) is preferred. Proven experience in scaling-up synthetic oligonucleotide syntheses and technology transfer to a GMP manufacturing facility is a plus. Candidate should be well-versed with International Council for Harmonization (ICH)/regulatory guidelines and their impact on process development of synthetic molecules and bioconjugates. Experience in working with multi-functional Chemistry, Manufacturing and Control (CMC) teams and experience in authoring publications, reports, technical transfer documents, regulatory support documents, patents is a plus.</p><p>Note: title will be commensurate with experience</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 16:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Physician Scientist – Obesity and Liver Disease Human Genetics]]></title>
    <date><![CDATA[Sun, 21 Sep 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39319]]></requisitionid>
    <referencenumber><![CDATA[R39319]]></referencenumber>
    <apijobid><![CDATA[r39319]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r39319/physician-scientist-obesity-and-liver-disease-human-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[<p>We are looking for an exceptional Physician Scientist to join our Cardiometabolic Therapeutic Area Genetics (TAG) team at the Regeneron Genetics Center (RGC). Within the RGC, the Cardiometabolic TAG team is using massive scale human exome sequencing for discovery and validation of new therapeutic targets in obesity and obesity associated metabolic disease. The position holder will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to accelerate therapeutic development for genetically-validated targets in obesity and metabolic disease via the generation of new human genetics and epidemiological insights.<br> </p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Accelerate therapeutic development for genetically-validated targets via the generation of new human genetics and epidemiological insights.</p></li><li><p>Generate key research questions and then design and execute studies and analyses to help address these questions, interpret the results of these studies and summarize ensuing insights in a variety of formats for different audiences (e.g. documents, presentations, patent applications, publications, etc.).</p></li><li><p>Understand and leverage RGC and Regeneron datasets, external resources and the scientific/medical literature to address key research questions at hand and summarize results giving appropriate weight to quantitative and qualitative strength of evidence.</p></li><li><p>Support target nominations and validation utilizing the RGC’s human genetics capabilities and leveraging Regeneron’s extensive internal therapeutics platforms and development modalities.</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><li><p>Participate in the intellectual life of the Cardiometabolic TAG, the RGC and Regeneron at large and help build an inclusive work culture where everyone can perform at their best and fully develop their talent and potential.</p></li><li><p>Represent the Therapeutic Area Genetics team in cross-functional initiatives within RGC and Regeneron.</p></li></ul><p><strong>This job might be for you if you have:</strong></p><ul><li><p>Demonstrated ability to design and lead human genetics and epidemiological studies delivering medically-relevant findings in a team-based environment.</p></li><li><p>Ability to use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions. Familiarity with clinical genetics concepts and various genetic models of disease.</p></li><li><p>Strong computational and quantitative skills including ability to design and execute complex analyses using large scale datasets both with individual-level as well as result-level data (e.g. UK Biobank, All of US, MVP, Biobank Japan, meta-analysis of genome-wide summary statistics, etc). This includes proficiency with R or similar software and familiarity with high performance computing environments.</p></li><li><p>Experience leading complex human genetics research endeavors. Knowledge of different study designs and analyses including GWAS, exome or genome sequencing in cohort, case-control or family-based studies. Ability to integrate different data resources to translate initial findings.</p></li><li><p>Familiarity with the applications of genetics to gain medically-actionable insights including polygenic risk scores, quantitative traits analyses and Mendelian randomization.</p></li><li><p>Understanding of drug development and clinical trial design and execution. Experience as investigator in Randomized Controlled Trials is a plus. Experience in the clinical management or medical research relating to cardio-metabolic disease is not strictly required but is a plus.</p></li></ul><p>.</p><p><strong>To be considered for this role,</strong> you must have a MD with strong background in and knowledge of human genetics and genetic epidemiology. An outstanding candidate will be an MD/PhD with training and experience in translational human genetics, genetic epidemiology, epidemiology (or related disciplines) and strong quantitative skills.</p><p>#MDJOBSGG #MDJobs</p><ul></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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$173,500.00 - $283,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Health Economics & Outcomes Research- Hematology Oncology]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41693]]></requisitionid>
    <referencenumber><![CDATA[R41693]]></referencenumber>
    <apijobid><![CDATA[r41693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41693/director-health-economics-outcomes-research-hematology-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>We’re seeking a strategic and scientifically insightful leader to join our Global HEOR team supporting Regeneron’s hematologic oncology portfolio. This newly created position within our expanding team you will build us HEOR strategies that help shape clinical development, regulatory decisions, and global market access for novel therapies. In this strategic role, you’ll partner with colleagues worldwide to bring significant innovations to patients while influencing the evolving landscape of value-based healthcare.</p><p>This position will be located at our Sleepy Hollow, NY location requiring you to be on-site 4 days/week. We are unable to provide a hybrid or fully remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following: </strong><br>• Developing and implementing global HEOR strategies for our leading hematologic oncology assets.<br>• Collaborating with cross-functional partners to strengthen product value propositions and support patient access.<br>• Leading design and execution of health economic models, value dossiers, and HTA submissions.<br>• Coordinating regulatory-grade real-world evidence studies and innovative RWD partnerships.<br>• Guiding development and validation of clinical outcomes assessments for integration into trials.<br>• Driving epidemiology analyses and observational studies to support development and commercial goals.<br>• Communicating HEOR insights to international teams, HTA bodies, and reimbursement decision-makers.<br>• Leading vendors and external experts to ensure high-quality HEOR results.</p><p>This role may be for you if you:<br>• Want to make a meaningful impact on patient lives through your work.<br>• Thrive in a fast-paced, collaborative environment.<br>• Enjoy a highly visible role that influences critical decisions.<br>• Work on ground breaking therapies in malignant hematology and oncology.<br> </p><p>To Be Considered<br>You will need an advanced graduate degree (Ph.D., MS, MD, PharmD, B. Pharm, or RN with master’s) in a HEOR-related subject area such as health economics, outcomes research, health services research, pharmacoepidemiology, epidemiology, or statistics. You should bring 7+ years of HEOR or related experience with a PhD, or 9+ years with an MS, including expertise in study design, health economic modeling, and COA development. Experience engaging with regulatory authorities and HTA agencies is essential, along with a strong publication record. Oncology HEOR experience (minimum 2 years) and familiarity with regulatory-grade RWE are highly preferred.<br> </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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$202,000.00 - $336,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Sun, 16 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43733]]></requisitionid>
    <referencenumber><![CDATA[R43733]]></referencenumber>
    <apijobid><![CDATA[r43733]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43733/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>The Senior Manager Statistical Programming provides technical leadership and support to the project teams on all statistical programming matters according to the project strategies within therapeutic area(s). The incumbent manages the programming aspect of a project in collaboration with partnering functions, stakeholders, and external functional service providers for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards, regulatory safety reports, and other requests. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. The incumbent will lead or participate in process and methodology development for department goals and SME topics. Maybe responsible for goal setting and performance management.</p><p><strong>In this role, a typical day might include: </strong><strong>​</strong></p><ul><li>Manage and lead programming support within multiple studies/projects in various study activities to ensures timely and high-quality programming deliverables in assigned projects and areas. Lead and coordinate programming documentation including specifications, as appropriate, for multiple studies following programming standards and processes</li><li>Demonstrate company values and act as a role model by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability</li><li>Ensure the commitment and reinforcement of the roles and responsibilities of the statistical programming function</li><li>Proactive communication with study and project teams to clarify requirements and specifications, guide direct reports or support programmers on assignment status</li><li>Lead and support global regulatory authority submissions including preparing programming deliverable for submission and working closely with partnering functions to address health authority requests.</li><li>Lead and manage department goals and SME topics</li><li>May oversee development of direct reports by setting goals, managing performance, evaluating, and monitoring training needs, supporting development plans, mentoring, and coaching</li><li>May participate in screening and interviewing candidates for contractor and permanent positions.</li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 10+ (12+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience.</li><li>Advanced SAS programming skills in a clinical data environment with expertise in at least one, preferably multiple, therapeutic areas. Knowledge of other programming languages such as R, Python etc. is a plus.</li><li>Understanding of pharmaceutical clinical development across multiple therapeutic areas (i.e. understanding of statistical concepts, techniques and clinical trial principles) and good knowledge of regulatory submissions and requirements</li><li>Ability to work on global interdisciplinary teams. Good organizational, interpersonal, communication, and leadership skills. Establish and maintain effective working relationships with coworkers, managers, and clients</li><li>Ability to effectively manage multiple tasks and projects</li><li>Problem solving and innovative skills that demonstrate initiative and motivation</li><li>Ability to influence others, mentor, and coach junior programmers to achieve results</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences, Hematology]]></title>
    <date><![CDATA[Mon, 24 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43843]]></requisitionid>
    <referencenumber><![CDATA[R43843]]></referencenumber>
    <apijobid><![CDATA[r43843]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43843/medical-director-clinical-sciences-hematology/]]></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 Medical Director, Clinical Sciences functions as clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), under leadership of Program Lead Medical Director (Program Lead MD) or Sr. Medical Director.</p><p>A day in the life may include the following responsibilities:</p><ul><li><p>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program with minimal supervision from Program Lead MD. </p></li><li><p>Manages all operational aspects and drives execution of the section of the clinical program in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates.</p></li><li><p>Supports Program Lead MD (and/or Sr. MD) and frequently lead interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards.</p></li><li><p>Serves occasionally as member for Global Clinical Development training programs, author or reviewer for clinical SOPs and may contribute to GCD strategy by serving on taskforces or other panels.</p></li></ul><p>This job may be for you if:</p><p>· You are passionate about impacting entire populations of patients</p><p>· You want to develop innovative new therapies</p><p>· You enjoy collaborating with team members towards a common goal.</p><p>In order to be considered for this position, you must have an MD or equivalent, ideally with Hematology Oncology fellowship training. More than 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV is strongly preferred. Medical/scientific expertise in disease area of assigned program is preferable. </p><p>#MDJOBS #heme</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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Integration Engineer]]></title>
    <date><![CDATA[Wed, 17 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44178]]></requisitionid>
    <referencenumber><![CDATA[R44178]]></referencenumber>
    <apijobid><![CDATA[r44178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44178/senior-automation-integration-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems.</p><p><strong>As a Senior Automation Systems Integration Engineer, a typical day might include the following:</strong></p><ul><li>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures.</li><li>Integration of industrial automation systems, business applications and enterprise data platforms.</li><li>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems.</li><li>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines.</li><li>Supporting small manufacturing, engineering, and validation projects.</li><li>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action.</li><li>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols.</li><li>Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure</li><li>Creation, modification, and maintenance of automation system documentation</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have experience with OT applications, including SCADAs, HMIs, Historians, etc.</li><li>Experience working with advanced technologies such as OPC UA, MQTT, IIOT platforms, and data integration tools to create a centralized, real-time data architecture that supports Industry 4.0 initiatives.</li><li>Are familiar with standing up large systems at the enterprise level</li><li>Have core knowledge related to ISE S95, S88 principles and IT/Automation integration</li><li>Have familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better</li><li>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly</li><li>Can balance changing priorities with increasing workload by making/communicating timely decisions</li></ul><p>To be considered for this position you ideally should have a bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level:</p><ul><li>Senior Engineer: 5+ years</li><li>Principal Engineer: 8+ years</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>#IRELIM #JOBSIEPR #LI-Onsite #REGNIRLTO </p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assistant General Counsel - FDA Regulatory & Commercial]]></title>
    <date><![CDATA[Tue, 13 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43371]]></requisitionid>
    <referencenumber><![CDATA[R43371]]></referencenumber>
    <apijobid><![CDATA[r43371]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43371/assistant-general-counsel-fda-regulatory-commercial/]]></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>This position with the Regeneron Regulatory and Commercial Law team will provide collaborative legal advice and counsel in connection with the commercialization of Regeneron’s products. They will also be part of a legal team supporting cardiovascular, hematology, rare disease, oncology, obesity, and new products. Counsel will be embedded as a core team member, serving as a strategic legal advisor to multiple internal collaborators, including the commercial, medical affairs, regulatory, HEOR, corporate affairs, and compliance teams.</p><p><strong>This role is based at Regeneron's offices in Sleepy Hollow, NY (4 days a week onsite) - it is not open to hybrid or fully remote assignments</strong></p><p><strong>As an Assistant General Counsel a typical day may include:</strong></p><ul><li><p>Providing day-to-day strategic and business-focused legal and risk counseling for Regeneron’s products/product candidates, from development through commercialization. Advising on a broad range of healthcare regulatory matters, including regulatory labeling discussions, advertising and promotion, drug safety, market research, scientific exchange, and interactions with healthcare professionals and patients.</p></li><li><p>Demonstrating a solid understanding of the strategic and tactical objectives of the client teams supported, and advising on strategic brand and medical planning, developing creative and innovative solutions to key initiatives, considering the business objectives and priorities, as well as the US and/or international legal and regulatory landscape.</p></li><li><p>Counseling on all aspects of product commercialization, including launch preparation, launch execution, market development, disease awareness, product communication, advertising and promotion, and strategic brand planning.</p></li><li><p>Ensuring compliance with all relevant laws, regulations, policies, procedure and controls within relevant business areas supported</p></li><li><p>Advising on data disclosures following clinical development milestones via press releases and US or international medical congresses and scientific exchange compliant with applicable laws and regulations.</p></li><li><p>Liaising with other Law Department functions both in the US and globally, including litigation, IP, Compliance, and Transactions, to ensure integrated legal support and timely updates and information sharing.</p></li></ul><br><h3><strong>This role may be for you if you have</strong>:</h3><ul><li><p>Previous experience as a product attorney at a pharmaceutical or biotechnology company preferred</p></li><li><p>Ability to handle multiple priorities in a dynamic and evolving environment</p></li><li><p>Excellent oral and written communication skills with a shown ability to present complex information accurately and concisely to influence others at all levels of management</p></li><li><p>Proven capacity to cultivate strong client relationships and influence leadership, including ability to assess and help business colleagues handle risks in a highly regulated environment</p></li><li><p>Strong analytical skills and demonstrated learning agility and a deep aptitude for science and data analysis</p></li></ul><p><strong>To be considered for this role, we are looking for candidates with </strong>a JD with excellent law school credentials. Be licensed to practice law in New York or be eligible for licensure as a registered in-house counsel. Have 10+ years of legal experience, including positions as an in-house attorney at a biotech/pharmaceutical company, and at a nationally recognized law practice in the area of pharmaceutical and healthcare law.</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>$238,400.00 - $397,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 14 Jan 2026 19:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs - Japan]]></title>
    <date><![CDATA[Sun, 25 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44572]]></requisitionid>
    <referencenumber><![CDATA[R44572]]></referencenumber>
    <apijobid><![CDATA[r44572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44572/manager-regulatory-affairs-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>As part of our global expansion, we are now looking for in-country regulatory professionals to join our growing global regulatory team. This is an exciting opportunity to demonstrate your knowledge in leading regulatory processes for biological products and regenerative medicines in Japan, and to build Regeneron’s profile with key stakeholders locally.</p><p>In this unique position you will interact with a wide and diverse range of colleagues across Regeneron, both locally, and globally.</p><p><strong>Key duties:</strong></p><ul><li>Execute the timely submissions of marketing applications and post-approval changes for assigned projects</li><li>Work with Japan Regulatory Lead to manage and oversee interactions with Japanese regulatory authorities</li><li>Maintain extensive knowledge of Japan’s Submission Requirements</li><li>Ensure compliance with Japan’s regulatory requirements and all appropriate local standards</li><li>Lead/support the timely preparation and submission of clinical trial applications to PMDA</li><li>Collaborate with and represent regulatory as part of a local multi-disciplinary team including clinical, commercial, medical, and patient safety colleagues</li><li>Assist the development of local labelling and patient information for assigned programs</li><li>Co-ordinate regulatory review of promotional materials as and when needed</li></ul><p><strong>Essential:</strong></p><ul><li>Bachelors degree in an appropriate scientific discipline</li><li>Experienced (approx. 5 years) regulatory professional having managed major submissions and approvals in Japan</li><li>Knowledge of clinical trial requirements and ability to problem-solve local procedures</li><li>Ability to advise on clinical aspects of local requirements will be a major advantage</li><li>Ability to think strategically, sound commercial awareness and excellent communication skills, both verbally and in written form in English.</li><li>Ability to thrive in and foster strong matrix team working in a global environment</li><li>Negotiation skills with Japanese Health Authorities</li><li>High fluency in English</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 26 Jan 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs (MSL) – Oncology]]></title>
    <date><![CDATA[Mon, 19 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44235]]></requisitionid>
    <referencenumber><![CDATA[R44235]]></referencenumber>
    <apijobid><![CDATA[r44235]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44235/associate-director-field-medical-affairs-msl-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>We are seeking an <strong>Associate Director, Field Medical Affairs (MSL) – Oncology</strong> to join our team and strengthen our partnerships with experts in Oncology. In this role, you will engage with key opinion leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. You’ll play a meaningful role in crafting the understanding of Regeneron’s therapies, supporting clinical development and investigator-initiated research, and contributing to impactful product launches.</p><p>We are looking for our next team member to join our passionate & dedicated Medical Affairs team in France.</p><p><strong>Associate Director, Field Medical Affairs (MSL), Oncology</strong></p><p><strong>Région Paris - Ile de France </strong></p><p><strong>A Typical Day:</strong></p><ul><li>Building and handling relationships with KOLs in Oncology.</li><li>Acting as a primary clinical/scientific contact for HCPs and investigators.</li><li>Sharing medical insights to advise strategy and development plans.</li><li>Supporting clinical trial execution by identifying investigators and trial sites.</li><li>Collaborating on abstracts, posters, and manuscripts to communicate data.</li><li>Contributing to investigator-initiated study programs and research collaborations.</li><li>Attending medical congresses to gather and report competitive intelligence.</li><li>Partnering cross-functionally with Medical Affairs, Commercial, and Market Access.</li></ul><p><strong>This Role May Be For You:</strong></p><ul><li>You thrive on scientific exchange and are confident discussing complex data with KOLs.</li><li>You have established connections in Oncology and understand the Immuno-Oncology landscape.</li><li>You enjoy balancing independent field work with cross-functional collaboration.</li><li>You adapt easily to changing priorities and field-based challenges.</li><li>You are motivated by opportunities to contribute to drug launches and new research.</li><li>You value compliance and integrity while working with investigators and partners.</li><li>You are comfortable with frequent travel and engaging in high-level conversations.</li></ul><p>To be considered, you should bring at least 5+ years of relevant experience with a minimum of 3+ years working as Field Medical or Medical Manager experience in biotech or pharma, with a strong background in Oncology. You hold a PhD, PharmD, MD or Doctor of Veterinary Medicine (DVM), Board Certified MD. Strong communication, organizational skills, and the ability to travel up to 70% are essential, so a valid driving licence is required.</p><p>Knowledge of Oncology is required, and experience in Immuno-Oncology is preferred. Drug launch experience and established KOL relationships are highly valued. You should also have solid knowledge of treatment guidelines, clinical research, and EU regulations.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 20 Jan 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[District Manager-Field Access (Southeast)]]></title>
    <date><![CDATA[Thu, 22 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44751]]></requisitionid>
    <referencenumber><![CDATA[R44751]]></referencenumber>
    <apijobid><![CDATA[r44751]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44751/district-manager-field-access-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The District Manager, Field Access and Reimbursement (DM) will be responsible for leading and managing the reimbursement field team in the Southeast for Regeneron. We expect the Manager to lead, coach, and manage a Field Reimbursement Manager team responsible for calling on office personnel, ensuring optimal access, effective pull-through, and educating on reimbursement services and program support in collaboration with the HUB services organization as it relates to the Regeneron product portfolio. We believe the DM will be tasked for the execution of reimbursement initiatives in the various therapeutic markets. We assume the manager to work with internal and external partners to ensure optimal coverage within the defined customer base.</div><div><div><div><div><h3><strong>A Typical Day Might Look Like This:</strong></h3><ul><li>Work with the Sales and Access leadership teams within REGN and Sanofi counterparts to lead Regional and local strategy for payer and provider access.</li><li>Develop and implement local tactical plans for execution of all access initiatives and relevant to defined needs in each respective customer market.</li><li>Lead and coach to identified measurable performance parameters and monitor performance against these agreed parameters.</li><li>Proactively collaborate and communicate with Sanofi partners to achieve brand goals and performance metrics.</li></ul><br><h3><strong>This Position Might Be for You If:</strong></h3><ul><li>Successful leadership record of hiring, coaching, developing, promoting, and retaining top talent within span of control and ability to effectively manage performance of the team.</li><li>Strong understanding of Payer environment, reimbursement and challenges within National, Regional and local payer market including; government programs, managed health care and evolving health care systems.</li><li>Ability to partner and collaborate with other internal field teams and alliance partners.</li><li>You are able to navigate a global environment with minimal support</li></ul><p>To be considered, we are looking someone who has managed a field reimbursement or sales team for 3 years with a minimum of 5+ years of sales experience prior to that. We also require you to have worked with Biologics and/or specialty pharmaceutical products. Lastly this is a role that covers a large territory and it is expected for you to travel to cover the territory.</p></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>$188,100.00 - $233,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 23 Jan 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology - Little Rock, AR, Oklahoma City, OK and Tulsa, OK]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44479]]></requisitionid>
    <referencenumber><![CDATA[R44479]]></referencenumber>
    <apijobid><![CDATA[r44479]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44479/medical-account-specialists-hematology-little-rock-ar-oklahoma-city-ok-and-tulsa-ok/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Arkansas]]></city>
    <state><![CDATA[Arkansas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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>A typical day may include the following:</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 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><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 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><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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Engineer, Data Science (PMPD)]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41337]]></requisitionid>
    <referencenumber><![CDATA[R41337]]></referencenumber>
    <apijobid><![CDATA[r41337]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41337/staff-engineer-data-science-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>The Data Enablement and Analytics (DEA) team within the PAPD (Product, Analytics and Process Development) organization drives PAPD’s digital transformation by making data usable, useful, and impactful in support of our mission of Transforming Therapeutic Molecules into Products for a Diversified Pipeline.</p><p>We are seeking a <strong>Staff Engineer, AI and Data Science </strong>to join our Artificial Intelligence and Advanced Analytics (AA) team in DEA, who pairs deep bioprocess‐engineering expertise with sophisticated AI/ML and Data Science (DS) capabilities to accelerate biologics development and manufacturing.<br> </p><p>You will design, implement, and operationalize AI and DS models for upstream (cell-culture/bioreactor), downstream (purification) operations, Formulation Development and multiple Analytics teams while partnering closely with process-development, manufacturing-sciences, and digital teams. You will turn data into prescriptive guidance, deploy production-grade models, and build innovative AI solutions that enhance process understanding, optimization, and automation.</p><p><br><strong>A Typical Day in the Role of Staff Engineer Might Look Like:</strong></p><ul><li>Build and deploy AI/ML-powered solutions to accelerate our digitalization journey.</li><li>Advance PAPD’s broader AI, DS and related digital-maturity initiatives.</li><li>Collaborate with process engineers, citizen data scientists, IT, and manufacturing colleagues to coordinate AI and Advanced modeling efforts enterprise wide.</li><li>Explore, prototype and implement GenAI approaches and solutions (e.g., Retrieval-Augmented Generation) to enhance knowledge management, and decision support.</li><li>Develop, validate, and maintain mechanistic, hybrid, and data-driven models for cell culture, purification, formulation and other processes.</li><li>Translate complex bioprocess questions into quantitative modeling strategies that inform scale-up, tech transfer, and continuous improvement.</li><li>Mentor citizen data scientists and champion best practices in model development, method selection, and code quality.</li></ul><p><strong>This Role Might Be For You If You Have:</strong></p><ul><li>Analytical rigor and creative problem solving</li><li>Ability to drive projects autonomously while thriving in cross-functional teams</li><li>Excellent written and verbal communication</li><li>Passion for innovation and continuous learning</li></ul><p>This role requires a Ph.D. in Chemical/Biochemical Engineering, Biotechnology, Applied Mathematics, Computer Science or related field with 2+ years of industrial experience OR- Master’s with 5+ years. Mechanistic understanding of upstream and/or downstream bioprocess unit operations, scale-up/down principles, and critical quality attributes is required. A demonstrated success modeling bioprocesses via first-principles, hybrid, or data-driven (ML) methods is preferred.</p><p>A strong foundation in AI/ML algorithms (regression, classification, Bayesian methods, deep learning, time-series, probabilistic modeling) is a plus, along with expertise in multivariate statistics for process modeling, real-time monitoring, and control. Expert programming proficiency in Python and SQL and experience with statistical/computational tools such as JMP, SIMCA, MATLAB is helpful. Proven ability to communicate technical concepts to multidisciplinary stakeholders a must. Experience with GenAI stacks (LLMs, vector databases, RAG pipelines) and multimodal techniques is necessary.</p><p><strong>Preferred Qualifications</strong></p><ul><li>Hands-on experience with cloud analytics platforms (e.g., Dataiku, Databricks).</li><li>Strong working knowledge of Quality-by-Design (QbD) principles and statistically rigorous Design-of-Experiments (DoE) for defining design space, optimizing critical process parameters, and informing robust control strategies.</li><li>Familiarity with PAT and chemometric modeling (e.g., Raman spectroscopy) for bioprocess monitoring and control.</li><li>Understanding of operation research techniques such as combinatorial optimization, linear programming, mixed integer programming is a plus.</li><li>Strong publication record in bioprocess modeling or AI for biomanufacturing.</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 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>$126,700.00 - $206,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I- Dermatology- Inland Empire, CA]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44981]]></requisitionid>
    <referencenumber><![CDATA[R44981]]></referencenumber>
    <apijobid><![CDATA[r44981]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44981/medical-specialist-i-dermatology-inland-empire-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[<p><strong>Medical Specialist, Dermatology, Inland Empire, CA (MS)</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Miami, FL]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45100]]></requisitionid>
    <referencenumber><![CDATA[R45100]]></referencenumber>
    <apijobid><![CDATA[r45100]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45100/medical-specialist-i-dermatology-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[<p><strong>Geography: Miami, FL</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.<br>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, CMC Regulatory Affairs (Hematology/Oncology)]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45185]]></requisitionid>
    <referencenumber><![CDATA[R45185]]></referencenumber>
    <apijobid><![CDATA[r45185]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45185/associate-director-cmc-regulatory-affairs-hematologyoncology/]]></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>As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.</p><p>For US locations Tarrytown,, NY this role is on-site 4 days in the office and 1 day from home. For Uxbridge, UK or Dublin, Ireland this role would be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position . If eligible, we can offer relocation benefits.</p><p><strong>A typical day may include the following: </strong><br>• Lead product development activities from a CMC regulatory standpoint with input from senior management.<br>• Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post-approval activities.<br>• Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work-arounds, and obtain consensus. <br>• Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.<br>• Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).<br>• Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents; <br>• Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.<br>• Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.<br>• Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.<br>• Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.<br>• Find opportunities to initiate operational changes and policy modifications.<br>• Manage and coach team member(s). </p><p><strong>This may be for you if you: </strong><br>• Have a strong grasp of CMC worldwide regulations and guidelines.<br>• Have been successful in building collaboration and teamwork across cross-functional teams.<br>• Can demonstrate a proven track record managing and mentoring people.<br>• Demonstrated skill in managing multiple priorities.</p><p><br>To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred. Proven track record supporting small molecule drugs and/or biological products through development and approval is a distinct advantage. It is required to have a good understanding of current CMC worldwide regulations and guidelines. Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.<br> </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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HEOR (Classical Hematology)]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45181]]></requisitionid>
    <referencenumber><![CDATA[R45181]]></referencenumber>
    <apijobid><![CDATA[r45181]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45181/associate-director-heor-classical-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>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 of our classical hematology portfolio. </p><p>This position is at our Sleepy Hollow, NY location and will require you to be onsite 4 days/week. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Develop and implement global HEOR strategies and programs for our portfolio 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 future patient access to our therapeutics<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 in support of development and regulatory goals.<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 future patient access. <br>• Develop and implement Clinical Outcomes Assessment (COA) measurement strategies and plans in support of product labeling, patient access and product differentiation. Develop and validate COA endpoints for integration in clinical studies; analyze and communicate data from clinical trials. Produce COA evidence dossiers for regulatory submissions. Interact as necessary with Agencies on those matters and keep track of competitor PRO developments with regulators and payers. <br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.</p><p><strong>This may be for you if you: </strong><br>• Want to have an impact on patient lives<br>• Enjoy working in a ‘rapid response’ environment<br>• Would like an opportunity to present to senior leaders<br>• Want to be part of a growing high performing team</p><p>To be considered it is required to have an Advanced graduate degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field (e.g. pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health). 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. Strong technical expertise required in design and conduct of HEOR studies and models. Solid understanding of regulatory (e.g. FDA, EMA) considerations. Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data.<br> </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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III Analytics Automation]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44817]]></requisitionid>
    <referencenumber><![CDATA[R44817]]></referencenumber>
    <apijobid><![CDATA[r44817]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44817/process-development-engineer-iii-analytics-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>The Preclinical Manufacturing and Process Development department is seeking an experienced professional to operate, maintain, and repair automated low- and ultra-low-temperature biobanks with a total capacity of approximately 4.3 million samples, supporting research and development efforts. In this exciting role, you will be collaborating with teams to manage and distribute large collections of research samples using both manual and automated cold storage technologies. You will also propose innovative ways to sample management workflows, implement preventative maintenance strategies, utilize data-driven decision-making, and evaluate new technologies to advance the collaborative automation of cold storage systems.</p><h3>A Typical Day in the Role Might Look Like:</h3><ul><li>Operate, maintain, and repair automated low- and ultra-low-temperature biobanks, ensuring continuous functionality and adherence to operational specifications.</li><li>Collaborate with sample management teams, Facilities Operations, and HVAC teams, vendor, and additional stakeholders to support uninterrupted operation of automated biobanking technologies and timely resolutions when technical troubleshooting is required.</li><li>Assist sample management teams with routine automated sample handling, distribution, and inventory management activities, which includes training team to troubleshoot equipment if/as needed.</li><li>Proactively supervise, document, and analyze equipment performance to ensure systems operate within defined specifications and performance thresholds.</li><li>Develop and prioritize recurring equipment maintenance schedules to minimize downtime and maintain system reliability.</li><li>Identify and implement new strategies and technologies to improve sample management workflows, including automation improvements and novel approaches to data integration.</li><li>Collaborate with IT groups to maintain and optimize existing software interfaces that support sample management capabilities, as well as platforms for acquiring, monitoring, and analyzing system performance data.</li></ul><h3>This Role Might Be For You If You Have:</h3><ul><li>Extensive expertise in automated biobanking cold storage technologies, with a strong understanding of mechanical, electrical, refrigeration, and control systems used in ultra-low-temperature environments.</li><li>Proven ability to operate, maintain, troubleshoot, and repair sophisticated automated biobanking cold storage systems, including robotic sample handling systems and associated software interfaces; experience with laboratory robotics and automation platforms is highly desirable.</li><li>Strong written and oral communication skills, with the ability to effectively engage and collaborate with stakeholders at all levels within a matrixed organization, including technical teams, management, and external vendors.</li><li>Preferred qualifications include demonstrated leadership abilities, prior mentorship experience, and a track record of successfully managing cross-functional projects or teams.</li></ul><p>This role requires a PhD with 0-3 years, a MS with 8+ or a BS with 10+ years proven experience. Experience with Liconic cold storage technologies and BiOLiX software is highly desirable.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 08:56:53 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Ancillary Supply Management]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45268]]></requisitionid>
    <referencenumber><![CDATA[R45268]]></referencenumber>
    <apijobid><![CDATA[r45268]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45268/senior-manager-ancillary-supply-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>As the <strong>Senior Manager of Ancillary Supply Management (ASM)</strong> you will be responsible for managing clinical ancillary supply and sourcing strategies at the asset, program, and study levels for Regeneron clinical trials. The Senior Manager will be part of an operational team that drives best practices, standardization, and optimization of ancillary supply strategies and purchasing processes. As part of Pharmacy Support Services team, the Senior Manager will collaborate with both internal and external stakeholders, including Global Development, Formulations Development, Industrial Operations, and Clinical Purchasing as well as external vendors to develop and drive the implementation of ancillary supply strategies in clinical trial settings as well develop innovative ancillary supply solutions. </p><p><strong>A typical day in this role looks like: </strong></p><p><strong>Lead Ancillary Supply Strategy & Planning</strong></p><ul><li>Serve as the lead ASM for assigned programs and studies, overseeing ancillary supply planning from early strategy through execution.</li><li>Drive cross‑portfolio ancillary supply planning, ensuring alignment with clinical development plans, study timelines, and operational needs.</li><li>Collaborate with external suppliers and vendors to perform financial evaluations of cost-effective sourcing alternatives for study-specific supply strategies. </li><li>Collaborate with Pharmacy Support Services, Clinical Study Teams, and Formulations Development to understand compatibility requirements and design optimized ancillary supply strategies.</li><li>Monitor supply availability, expiries, recalls, calibration and inspection needs, and risk‑mitigation activities.</li></ul><p><strong>Study Team & Cross‑Functional Leadership</strong></p><ul><li>Represent Ancillary Supplies on cross‑functional study teams.</li><li>Build strong, solutions‑oriented partnerships with key stakeholders and act as an escalation point for ancillary supply matters.</li><li>Support internal and external regulatory inspections; may represent the function during audits.</li><li>May mentor or coach junior Clinical Drug Supply & Logistics staff. May supervise staff.</li></ul><p><strong>Vendor & Budget Oversight</strong></p><ul><li>Lead vendor management including performance oversight, timelines, deliverables, and cost controls.</li><li>Partner with Global Procurement and Vendor Relationship Management to support SOWs, budgets, contracts, and KPI/KQI tracking.</li><li>Conduct financial assessments to identify cost‑effective sourcing alternatives.</li></ul><p><strong>Process Innovation & Functional Excellence</strong></p><ul><li>Lead or contribute to continuous improvement initiatives to meet business needs, SOP/WI development, and internal standards.</li><li>Create and support training of clinical teams and CDS&L team members on procedures and improvements.</li><li>Contribute to database and tracking system enhancements to improve operational transparency and performance.</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><strong>8+ years</strong> of relevant biotech/pharmaceutical industry experience, including <strong>5+ years</strong> specifically in clinical supply chain management with expert knowledge of medical/ancillary supply chains.</li><li>Proven experience translating complex clinical protocols into scalable, compliant supply strategies.</li><li>Strong understanding of global supply chain operations, clinical regulations, timelines, and logistics.</li><li>Exceptional communication, influencing, negotiation, and problem‑solving skills across diverse functional and geographic teams. Ability to work independently as well as a collaborative team environment.</li><li>Demonstrated integrity, decision‑making capability, and ability to perform under pressure.</li><li>Ability to generate trust by demonstrating the highest level of consistency between communications and associated output.</li></ul><p><strong>In order to be considered qualified for this role, </strong>a minimum of a Bachelor’s degree and <strong>8+ years</strong> of relevant biotech/pharmaceutical industry experience, including 5+ years specifically in clinical supply chain management with expert knowledge of medical/ancillary supply chains.</p><ul><li>A Master’s, MBA, or PharmD preferred; candidates with an advanced degree may qualify with <strong>5+ years</strong> relevant industry experience.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Market Access]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42974]]></requisitionid>
    <referencenumber><![CDATA[R42974]]></referencenumber>
    <apijobid><![CDATA[r42974]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42974/senior-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[<p>As a <strong>Senior Manager, Market Access</strong>, you will play a pivotal role in ensuring rapid and sustainable patient access to life-changing treatments in Japan. Your expertise in pricing and reimbursement strategy will shape national payer strategies and guide NHI price negotiations, bridging global market access insights with Japan-specific needs. This is an opportunity to make a meaningful impact while collaborating with cross-functional teams and driving innovation in the healthcare landscape.</p><p><strong>A Typical Day:</strong><br>As a Senior Manager, Market Access, your daily responsibilities will include:</p><ul><li>Leading local-level market access strategies for rare disease portfolios, ensuring alignment with global and regional priorities.</li><li>Acting as the interface between global and Japan affiliates to ensure seamless communication on strategy, evidence, and policy.</li><li>Driving pricing and reimbursement submissions to NHI price listings, including preparing reimbursement dossiers and executing price negotiations aligned with product strategies.</li><li>Monitoring policy shifts and pricing/HTA rules changes to assess potential impacts on business and providing Japan-specific insights to shape value and evidence plans.</li><li>Developing and maintaining reimbursement tracking tools to monitor progress and outcomes.</li><li>Establishing trade and distribution approaches in Japan that align with patient needs and local regulations.</li><li>Building and nurturing external relationships with key stakeholders such as MHLW, HTA bodies, and KOLs.</li><li>Representing Japan in global governance forums, access strategy teams, and launch readiness reviews to ensure country-specific needs are reflected in global planning.</li></ul><p><strong>This Role May Be For You If:</strong><br>You are someone who:</p><ul><li>Thrives in a collaborative environment and values cross-functional teamwork.</li><li>Has a strategic mindset and enjoys shaping policies that drive impactful outcomes.</li><li>Demonstrates strong project and process management skills, effectively prioritizing critical tasks in a dynamic setting.</li><li>Possesses in-depth knowledge of Japan’s reimbursement environment, payer systems, and policy trends.</li><li>Excels in negotiation and has experience interacting with authorities in Japan.</li><li>Is detail-oriented and adept at developing actionable insights from complex data.</li><li>Has experience in rare disease, cell, or gene therapy launches and understands the nuances of trade and distribution channels.</li><li>Communicates fluently in both Japanese (native level) and English (business level).</li></ul><p><strong>To Be Considered:</strong><br>We are looking for candidates with:</p><ul><li>A bachelor’s degree and at least 8 years of in-country market access experience.</li><li>Proven expertise in cost comparator pricing methodology and familiarity with HTA processes in Japan.</li><li>Strong initiative, critical thinking skills, and the ability to navigate a complex and evolving environment.</li><li>Preferred qualifications include rare disease, cell, or gene therapy launch experience, and familiarity with trade and distribution channels.</li></ul><p>Join us in shaping the future of healthcare and making a difference in the lives of patients. Apply today to be part of a team that values innovation, collaboration, and impact</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Data Management Portfolio Delivery - Oncology/Hematology]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45424]]></requisitionid>
    <referencenumber><![CDATA[R45424]]></referencenumber>
    <apijobid><![CDATA[r45424]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45424/senior-director-data-management-portfolio-delivery-oncologyhematology/]]></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 is seeking a Senior Director, Data Management Portfolio Delivery for our Oncology/Hematology therapeutic areas.</p><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>The Senior Director, Data Management Portfolio Delivery is a member of the Data Management Senior Leadership Team (DMSLT) and contributes to the vision, direction and strategy of the line function in support of the advancement of Regeneron’s clinical pipeline globally. The incumbent will be responsible for leading, managing and developing a team of highly engaged data managers and portfolio leads. Additionally, this role is accountable for effective oversight and timely delivery of all clinical data management activities from study start-up through archival across multiple studies in one or more therapeutic area(s) ensuring fit-for-purpose clinical data and compliance with Regeneron procedures and applicable regulatory requirements. </p></li><li><p>This position requires advanced knowledge of Electronic Data Capture systems, related applications, industry standards and regulatory requirements as well as progressive experience working on Phase I-IV studies and participating in regulatory submissions and health authority inspections within the medical device and/or pharmaceutical industry. </p></li><li><p>The Senior Director, Data Management Portfolio Delivery will collaborate closely with the Clinical Data Management Central Services, Clinical Data Operations and External Data Acquisition and Delivery Teams along with internal stakeholders and external vendors at different levels to ensure continuous improvement and successful outcomes for studies/programs. </p></li></ul><p><strong>This role might be for you if you can/have: </strong><strong>​</strong></p><ul><li><p>Contribute to the overall vision, direction and strategy for Data Management line function and assigned therapeutic area(s). </p></li><li><p>Accountable for operational execution and delivery of quality, fit-for-purpose data in support of statistical analyses across studies within assigned therapeutic area(s); provide comprehensive and effective oversight of FSPs and external partners. </p></li><li><p>Perform evaluation of resource demand and allocation across studies/programs to ensure adequate staffing and high levels of productivity in support of departmental objectives and corporate level portfolio delivery goals; select and recruit top industry talent and provide constructive performance appraisals to ensure professional growth and development. </p></li><li><p>Monitor group’s performance with respect to quality, adherence to standards, compliance with the established SOPs, WIs and applicable regulations; ensure continuous inspection readiness. </p></li><li><p>Proactively identify issues and propose solutions to mitigate operational risks and/or escalations for the function; provide strong leadership support for critical study data management milestones. </p></li><li><p>Lead strategic cross-functional initiatives to promote increased process efficiency and operational excellence; drive optimization of technology, systems and processes focusing on decreased cycle times, improved quality and inspection readiness. </p></li><li><p>Liaise with internal and external stakeholders to foster strong relationships and ensure effective cross-functional collaboration and communication throughout drug development process. </p></li><li><p>Author and contribute to the development of global clinical data management SOPs/WIs and corresponding departmental training curricula. </p></li><li><p>Demonstrate company values and act as a role model by promoting competence, collaboration, innovation, respect, ownership and accountability. </p></li><li><p>Maintain awareness of Clinical Data Management emerging trends, technology solutions and industry best practices through peer relationships with thought leaders in the industry; represent Regeneron in professional associations and forums. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor's Degree required, Advanced degree desirable. </p></li><li><p>15+ years of clinical data management experience in a pharmaceutical or biotech setting. </p></li><li><p>10+ years of functional leadership </p></li><li><p>8+ years of people management, leadership and mentoring experience </p></li><li><p>Leadership experience in Clinical Data Management or related field, leading midsized global data management groups across various therapeutic areas. </p></li><li><p>Expertise in clinical data management processes, industry best practices and clinical data systems (EDC, eSource, eCOA, IRT, Clinical Data Repository, medical terminology coding solutions, laboratory normal range repositories). </p></li><li><p>Advanced knowledge of clinical data management principles, technologies, regulations and best practices, including 21 CFR Part 11, ICH-GCP Guidelines, GxP compliance and GDPR, related to data acquisition, processing, handling and reporting used in drug development. </p></li><li><p>Healthcare business acumen with a comprehensive understanding of the pharmaceutical industry. </p></li><li><p>Demonstrated success in solving complex business problems, strategic thinking, organizational design, leading through periods of significant change, i.e., operating model shifts, dynamic portfolio expansion, company and/or asset acquisitions. </p></li><li><p>Ability to build relationships with key internal and external stakeholders at leadership levels and across levels by negotiating effectively, managing conflicts, escalations and collaborating successfully. </p></li><li><p>Proven ability to establish highly motivated and performing teams with a focus on transformation, innovation and operational excellence. </p></li><li><p>Excellent interpersonal, oral, and written communication skills. </p></li><li><p>Ability to adjust in a fast-paced environment. </p></li><li><p>May require up to 25% travel.</p></li></ul><div><div><ul><li><div><div><div><p>#GDBDMJobs</p></div></div></div></li></ul></div></div><div><div><ul></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 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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-New Orleans (North), North Shore (Hattiesburg, MS, Meridian, MS)]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45102]]></requisitionid>
    <referencenumber><![CDATA[R45102]]></referencenumber>
    <apijobid><![CDATA[r45102]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45102/medical-specialist-i-dermatology-new-orleans-north-north-shore-hattiesburg-ms-meridian-ms/]]></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>Geography: New Orleans North (Hattiesburg, MS, Meridian, MS)</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 12:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Business Operations (IT)]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42096]]></requisitionid>
    <referencenumber><![CDATA[R42096]]></referencenumber>
    <apijobid><![CDATA[r42096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42096/vice-president-business-operations-it/]]></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>We are currently looking to fill a Vice President position in our Business Operations organization to lead both the strategic transformation and daily operational management of all information technology functions supporting Manufacturing operations at Regeneron. This role encompasses dual leadership responsibilities—managing established IT functional areas while simultaneously leading implementation of new critical and migration from old to new systems across global operations sites.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Global IT Leadership: Lead IT functions such as Application Management, Infrastructure, Data, Digital Products, Software Development, Compliance, and Security. Ensure high system performance for manufacturing-critical systems.</p></li><li><p>Strategic Transformation: Jointly with respective function leaders, plan transformation of key processes and coordinate implementation of core systems (MES, LIMS, eQMS, ERP, etc.) to deliver significant uplift in operational performance of respective functions and cross functional processes.</p></li><li><p>Digitization: Collaborate with core business functions to design and implement digital data solutions to enable business intelligence and advanced analytics</p></li><li><p>Compliance & Risk Management: Ensure alignment to FDA, cGMP, and global regulations while mitigating IT risks.</p></li><li><p>Corporate Collaboration: Partner with Corporate IT for enterprise alignment while maintaining operations-specific independence.</p></li><li><p>Organizational Development: Build and develop a high-performing global IT team, ensuring internal availability of critical development capabilities, while outsourcing occasional and non-critical work, encouraging continuous improvement.</p></li><li><p>Budget & Vendor Management: Manage IT budgets and vendor relationships for seamless system integration, selective outsourcing of non-core and temporary activities for cost and performance optimization</p></li><li><p>Executive Leadership: Represent IT in Site Management teams and communicate progress to collaborators.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have led implementation and migration of core IT systems in operations and other business-critical functions, enterprise applications.</p></li><li><p>Have solved major business challenges and significantly improved business outcomes through identification, design and successful deployment of the newest information technologies and solutions.</p></li><li><p>Led successful digitization and automation of processes, data integration, development of business intelligence and AI solutions.</p></li><li><p>Are able to lead global teams that include IT and business partners, to manage dual operational/strategic responsibilities, and to drive cross-functional change initiatives.</p></li><li><p>Have strong interpersonal skills to collaborate across all organizational levels.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in IT or related field, 20+ years of experience in IT and business operations / transformations; biotechnology/pharmaceutical experience is a plus.</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>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Scientific Communications (Neurology)]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45314]]></requisitionid>
    <referencenumber><![CDATA[R45314]]></referencenumber>
    <apijobid><![CDATA[r45314]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45314/associate-director-scientific-communications-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>As an Associate Director, Scientific Communications, you will drive the development and alignment of our scientific communications plans for our Neurology Global Medical Affairs strategy. The primary responsibilities are to develop global scientific communications platforms and implement comprehensive and integrated medical communication plans. This includes ensuring the value, quality, and impact of all projects and the alignment of medical communications with internal and external partners.</p><p>This position can be at our Warren, NJ or Sleepy Hollow, NY offices and will require you to be on-site 4 days/week. We cannot offer a remote work option. If eligible we can offer relocation benefits. </p><p>A typical day may include the following<br>• Identifying and prioritizing scientific educational opportunities to reach targeted partners in an impactful manner.<br>• Collaborating with the Scientific Communications Lead and Franchise Medical Affairs Director(s) driving quality control and endorsement of: Scientific Communication Platforms, Lexicons, Disease-State Education materials, Program Slides, Data/Publication updates, Congress materials.<br>• Collaborating to develop medical content for congresses, and leading some of these activities<br>• Leading projects through medical review committees for approval of materials<br>• Ensuring medical and scientific integrity and accuracy of all assets, ensuring materials have a fair and balanced representation<br>• Developing centralized, organized, and searchable resource repositories for internal teams<br>• Managing vendor interactions, ensuring the scientific quality of projects and that goals are met in a timely manner<br>• Working with Project Managers to supervise all materials are delivered within the allocated budget, and tracks budget spend in a systematic manner</p><p>This may be for you if: <br>• You have a “patient first” value system<br>• Understand the complexities of scientific communications<br>• Have made innovative contributions affecting healthcare</p><p>To be considered for this position, you are required to have a PhD, MD, or PharmD along with >6 years experience in the pharmaceutical industry, including >4 years in Scientific Communications. A strong background in Neurology or Rare Disease is preferred. Any experience with launch activities, congress strategy/management or digital content development and dissemination is helpful.<br> </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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Statistical Genetics]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45060]]></requisitionid>
    <referencenumber><![CDATA[R45060]]></referencenumber>
    <apijobid><![CDATA[r45060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45060/senior-manager-statistical-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[<p>We are seeking a highly motivated and talented Senior Manager, Analytical Genetics and Data Science (AGDS) to join the AGDS team at the Regeneron Genetics Center (RGC). In this individual contributor role, you will conduct analyses of large-scale human genetic and phenotypic datasets for the discovery and validation of new therapeutic targets. Your work will use both in-house and public data resources, and your responsibilities will include integrating genetic data with other multi-omics data, applying state of the art statistical tools and methodologies, performing QC, and identifying and interrogating data driven hypotheses related to analytic and translational genetics. In addition to designing and executing analytic studies, you will collaborate with groups across Regeneron’s R&D functions, including both pre-clinical and clinical development teams.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Demonstrated expertise in genetic association analyses using large-scale genetic data. </p></li><li><p>Strong understanding of multi-omic data integration and its application in therapeutic target discovery. </p></li><li><p>Experience in developing and implementing methods for data harmonization and normalization. </p></li><li><p>Experience with cutting edge genetic analysis approaches, such as genome-wide association analysis, exome-wide association analysis, rare variant analysis, Mendelian randomization, LD Score regression, polygenic risk score modelling, pleiotropy analysis, meta-analysis, and the use of functional data to prioritize variants and genes of interest.</p></li><li><p>Proven ability to independently lead and manage 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></ul><p><strong>This role might be for you if have:</strong></p><ul><li><p>A PhD in a relevant field (e.g., statistical genetics, bioinformatics, computational biology, genetics, or related disciplines). </p></li><li><p>5 years of post-PhD experience in analyzing large-scale omics datasets.</p></li><li><p>Outstanding communication skills and an ability to summarize and present the results of human genetic studies to a variety of technical audiences, ranging from specialists in statistical genetics and computation to specialists in biology, drug design, and medicine.</p></li></ul><p>​#RGC</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Staff Engineer, AI and Advanced Analytics]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45059]]></requisitionid>
    <referencenumber><![CDATA[R45059]]></referencenumber>
    <apijobid><![CDATA[r45059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45059/sr-staff-engineer-ai-and-advanced-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>The Data Enablement and Analytics (DEA) team within the PAPD (Product, Analytics and Process Development) organization drives PAPD’s digital transformation by making data usable, useful, and impactful in support of our mission of Transforming Therapeutic Molecules into Products for a Diversified Pipeline.</p><p><br>We are seeking a hands-on Artificial Intelligence (AI), Machine learning (ML) and Advanced Analytics Leader to design, build, and deploy cutting-edge AI/ML solutions that accelerate PAPD’s mission. The Senior Staff Engineer combines deep technical expertise with architectural leadership, cross-functional collaboration, and team mentorship. The ideal candidate thrives at the intersection of science, data, and technology, and is passionate about driving innovation across PAPD.</p><p><strong>A Typical Day in the Role May Involve Aspects Of:</strong></p><p><strong>AI/ML & GenAI Development</strong></p><ul><li>Design and develop end-to-end AI/ML and Generative AI solutions, including LLM applications, RAG pipelines, and multimodal Agentic AI systems. </li><li>Contribute <strong>hands-on</strong> to prototyping, experimentation, model development, and production deployment.</li><li>Evaluate emerging GenAI tools, frameworks, and architectural patterns, recommending their adoption where appropriate.</li></ul><p><strong>Deliver Data Science Solutions</strong></p><ul><li>Build and deploy advanced data science models for diagnostic, predictive, and prescriptive use cases supporting PAPD scientific and operational workflows.</li><li>Apply statistical modeling, multivariate analysis, machine learning, time-series forecasting, feature engineering, and optimization methods to solve complex scientific and process challenges.</li><li>Collaborate with process scientists to design experiments, analyze process data, and translate insights into actionable recommendations.</li><li>Promote rigorous scientific methodology and strong statistical foundations across modeling efforts.</li></ul><p><strong>Architecture & Cross-Functional Collaboration</strong></p><ul><li>Partner with IT, Data Engineering, Other teams and departments, PAPD scientists, and analytics teams to define solution architectures and integrate models into enterprise workflows.</li><li>Translate scientific and operational challenges into scalable AI/ML solutions with clear business value.</li><li>Influence PAPD’s digitalization roadmap and contribute to long-term AI strategy.</li><li>Establish and champion best practices for model development, validation, MLOps, and responsible AI.</li></ul><p><strong>Team Leadership & Mentorship</strong></p><ul><li>Manage and mentor a team of data scientists and AI engineers.</li><li>Provide technical guidance, project oversight, and code reviews.</li><li>Support decentralized analytics (e.g., citizen data scientists) by providing frameworks, tools, and best practices.</li></ul><p><strong>Thought Leadership & Innovation</strong></p><ul><li>Stay current with advancements in AI/ML and GenAI, bringing forward opportunities for automation, decision support, knowledge management, and efficiency gains.</li><li>Lead or contribute to ideation sessions, proof-of-concepts, and Agile delivery initiatives across PAPD.</li></ul><p><strong>Minimum Qualifications</strong></p><ul><li>Ph.D. with 6+ years OR Master’s with 10+ years in Computer Science, Data Science, Data Engineering, Applied Mathematics, Bioinformatics, or related discipline.</li><li>Hands‑on experience building and deploying ML and GenAI models (e.g., deep learning, NLP, LLMs, RAG, multimodal models).</li><li>Strong programming proficiency in Python and familiarity with ML/GenAI frameworks (PyTorch, TensorFlow, Hugging Face, LangChain, vector databases).</li><li>Experience deploying solutions on cloud analytics platforms (Databricks/Dataiku/Azure/AWS).</li><li>Proven ability to communicate complex technical concepts to diverse stakeholders.</li><li>Demonstrated experience managing and coaching team members.</li></ul><div></div><p><strong>Preferred Qualifications</strong></p><ul><li>Experience in biopharma, process development, or scientific/operational analytics.</li><li>Knowledge of mechanistic, empirical, or hybrid modeling approaches.</li><li>Familiarity with PAT, chemometrics, multivariate analysis, or process analytics.</li><li>Experience with MLOps, CI/CD, containerization, API development, and distributed computing.</li></ul><div></div><p><strong>Core Competencies</strong></p><ul><li>Technical Leadership & Innovation</li><li>Strategic Thinking</li><li>Cross-Functional Collaboration</li><li>Communication & Influence</li><li>Ownership & Delivery</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist II-Phoenix Central, AZ]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45640]]></requisitionid>
    <referencenumber><![CDATA[R45640]]></referencenumber>
    <apijobid><![CDATA[r45640]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45640/oncology-account-specialist-ii-phoenix-central-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>Geography: Phoenix Central, AZ</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>A typical day may include the following:</strong></p><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><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 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). 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. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. 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. 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><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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. AI Engineer]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44471]]></requisitionid>
    <referencenumber><![CDATA[R44471]]></referencenumber>
    <apijobid><![CDATA[r44471]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44471/sr-ai-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Bengaluru]]></city>
    <state><![CDATA[Karnātaka]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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 Senior AI Engineer with deep AI expertise to join our AI & ML Engineering team. This role spans the full development stack — from designing intuitive, responsive front-end experiences to building robust, scalable backend services and data pipelines that power enterprise AI solutions. You will work on advanced projects involving LLM integration, RAG-based architectures, and cloud-native deployments, delivering end-to-end AI-driven products that are performant, reliable, and production-ready.</p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Build responsive, modern web interfaces using Next.js and React.js, including server-side rendering, static generation, and micro front-end architecture. Translate AI-driven data and insights into intuitive user experiences and interactive dashboards.</p></li><li><p>Design, develop, and maintain microservices using Python and Fast API for AI and ML workflows, ensuring scalability, security, and enterprise-grade reliability.</p></li><li><p>Integrate LLM capabilities (OpenAI, Anthropic, Google) directly into full-stack features, enabling conversational interfaces, intelligent search, and AI-assisted workflows.</p></li><li><p>Build and optimize data ingestion pipelines for structured and unstructured data sources to power AI models and analytics.</p></li><li><p>Create secure, high-performance RESTful APIs that bridge front-end experiences with backend AI/ML services and internal LLM access layers.</p></li><li><p>Implement Retrieval-Augmented Generation workflows and manage vector databases (Milvus) to power intelligent, context-aware applications.</p></li><li><p>Deploy and manage full-stack services in AWS EKS Kubernetes clusters, ensuring scalability, resilience, and uptime.</p></li><li><p>Deploy and manage full-stack services in AWS EKS Kubernetes clusters, ensuring scalability, resilience, and uptime.</p></li><li><p>Partner closely with ML engineers, data scientists, UX designers, and business stakeholders to deliver cohesive, AI-powered product experiences.</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Possess a Bachelor’s or Master’s degree in Computer Science, Software Engineering, or a related field.</p></li><li><p>5+ years of relevant experience in building AI-powered UI components using Next.js/React.js such as chat interfaces, semantic search, and real-time AI output streaming.</p></li><li><p>Advanced proficiency in Python (Fast API) for backend microservice development.</p></li><li><p>Strong proficiency in Next.js and React.js for building dynamic, responsive front-end interfaces, including SSR, SSG, and micro front-end architectures.</p></li><li><p>Deep understanding of RESTful API design, microservices architecture, and full-stack integration patterns.</p></li><li><p>Experience with Kubernetes, AWS EKS, and containerized full-stack deployments.</p></li><li><p>Hands-on experience with LLM integration (OpenAI, Anthropic, Google) and prompt engineering.</p></li><li><p>Familiarity with vector databases (Milvus) and RAG-based architectures.</p></li><li><p>Solid understanding of SQL and data pipeline engineering for AI workflows.</p></li><li><p>Jenkins, Bitbucket, Atlassian suite (Jira, Confluence).</p></li><li><p>Familiarity with image processing workflows and SQL data integration.</p></li><li><p>Knowledge of pharmaceutical industry standards and compliance practices.</p></li><li><p>Experience with Next.js App Router, state management libraries (Redux, Zustand), and modern front-end tooling.</p></li><li><p>Background in UX/design principles for enterprise AI product interfaces.</p></li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 04:26:19 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44857]]></requisitionid>
    <referencenumber><![CDATA[R44857]]></referencenumber>
    <apijobid><![CDATA[r44857]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44857/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>A <strong>Manager Statistical Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management.<br> </p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Develop an expertise within a therapeutic area or standard tool. Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project</li><li>Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)</li><li>Manage the effort, including esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Provide programming support for complex presentations and more complex statistical ad-hoc requests. </li><li>Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.</li><li>If applicable, lead an application development and act as the programming representative to the user audience.</li><li>Work with management to determine resource requirements for therapeutic area or department function <br>responsibilities. </li><li>Review and select resumes, screen and interview candidates for contractor and permanent positions.</li><li>Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals.</li><li>Advises all direct reports about the procedures surrounding retention of data, records, and information for <br>employees in their group.<br> </li></ul><p><strong>In order to be considered qualified for this role</strong></p><ul><li>Master’s Degree</li><li>8-10 years of relevant work experience</li><li>SAS Certification desirable.</li><li>Also acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal, IT Operations Management]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42989]]></requisitionid>
    <referencenumber><![CDATA[R42989]]></referencenumber>
    <apijobid><![CDATA[r42989]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42989/principal-it-operations-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><strong>Principal – IT Operations Management (Warren, NJ)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks a Principal – IT Operations Management (Warren, NJ) to design and implement the critical IT change and release management processes, work instructions, policies and activities in compliance with the information technology infrastructure library (ITIL) V3 framework. Design Change & Release functional design/requirements, policy, and procedures. Develop the Change & Release management workflows (for tools). Train team on change and release management processes and Agile, Scrum, and DevOps practices. Local telecommuting permitted up to 2 days per week.</p><p>SALARY RANGE: $150,550.00 - $184,700.00 per year</p><p><strong>Job Requirements</strong><strong>:</strong></p><p>Requires a Bachelor’s degree or foreign equivalent in Computer Science, Information Technology, or a related field and 2 years of Change and Release Management experience. Must have experience with: Designing and implementing the processes, work instructions and activities in compliance with the information technology infrastructure library (ITIL) V3 framework; Writing clear, concise, and accurate process documentation (i.e., knowledge article, Change & Release functional design/requirements, policy, and procedures); Developing and maintaining precise process documentation and accurate usage of the Change & Release management tools; Administration skills in ServiceNow; ServiceNow change & Release module and all supported ITSM processes; ServiceNow Platform; JIRA, SharePoint, DevOps tools such as SVN (subversion, source code repository), Continuous Integration tool (Hudson, Jenkins) and other IT tracking tools; Configuration, Incident, Request, and Problem management standards and methodologies; Service management principles; SDLC processes involving multiple engineering efforts; Excel reporting; IT Infrastructure, Virtualization, Security, App/Dev, Cloud Models and Technological Change; and Agile, Scrum, and DevOps practices. Will accept 2 years of work experience in lieu of the degree requirement. Will accept any suitable combination of education, training or experience.</p><p>We have an inclusive & diverse culture that provides comprehensive benefits, which often incl (depending on location) health/wellness programs, fitness centers, equity awards, annual bonuses, & PTO for eligible employees at all levels. See <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a> for details.</p><h3>Apply at https://careers.regeneron.com; Reference code: R42989.</h3><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 12:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Protein Expression Sciences]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45723]]></requisitionid>
    <referencenumber><![CDATA[R45723]]></referencenumber>
    <apijobid><![CDATA[r45723]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45723/senior-associate-scientist-protein-expression-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>We are looking for a Senior Associate Scientist to join the Protein Expression Sciences team. The candidate will be responsible for the operation of automated liquid handlers to support our VelociMab antibody discovery efforts. The candidate performs high throughput cloning and isolation of potential therapeutic antibodies. In addition to experience with liquid handling platforms, the successful candidate will have experience with general molecular biology and cell biology techniques.</p><p><strong>In this role, a typical day may include:</strong></p><ul><li><p>Performing high throughput molecular biology techniques including PCR, cloning and DNA isolation. </p></li><li><p>Operating and troubleshooting automated protocols on automated systems from but not limited to Hamilton Robotics and HighRes Biosolutions.</p></li><li><p>Seeding and transfecting of CHO transient cell lines on automated platform.</p></li><li><p>Data recording in ELN (electronic lab notebook) and LIMS</p></li></ul><p><strong>This role may be for you if you: </strong></p><ul><li><p>Enjoy working in a fast-paced environment.</p></li><li><p>Exhibit adept technical and problem-solving skills.</p></li><li><p>Have excellent communication and organizational skills, exhibit meticulous attention to detail.</p></li><li><p>Are comfortable working in a dynamic environment where priorities can change from day to day.</p></li></ul><p><strong>To be considered for this role, you must have: </strong> B.S with 2+ years of laboratory experience or M.S. in Molecular Biology, Cellular Biology, Biology, or related field. Experience with general molecular biology skills such PCR, DNA sequencing, mutagenesis, plasmid subcloning and mammalian cell transfection. Familiarity with automated liquid handlers is desired (preferably Hamilton Stars and Vantages). Experience in high-throughput assays is a plus. strong communication and organizational skills are also required.</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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Biostatistics - Medical Affairs]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46051]]></requisitionid>
    <referencenumber><![CDATA[R46051]]></referencenumber>
    <apijobid><![CDATA[r46051]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46051/senior-manager-biostatistics-medical-affairs/]]></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 seeking a Senior Manager, Biostatistics - Medical Affairs to join our team!</p><p>The Senior Manager of Biostatistics will be responsible for statistical support for Immunology & Inflammation within Medical Affairs and cultivate strong partnerships to enable effective cross-functional collaboration with other product team members from internal groups including BDM, Medical Affairs/HEOR, Clinical Development, Regulatory Affairs and other functions as needed. In addition, the Senior Manager of Biostatistics will support collaborations with external partners (e.g. CROs, industry consortiums, key opinion leaders). They will work with the Medical Affairs Biostatistics therapeutic area lead for Immunology & Inflammation to drive and establish best practices to support Immunology & Inflammation program continuous growth and Life Cycle Management (LCM) needs.</p><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>Interacts with Medical Affairs functional area colleagues including but not limited to Medical Directors, HEOR, Publications, Medical Information, Scientific Communication and other functional area colleagues like Clinical Scientists, Statistical Programming, Data Management, Medical Writing, and others for evidence generation efforts and HTA support including external collaborators.</p></li><li><p>Develops individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.</p></li><li><p>Collaborates with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting. </p></li><li><p>Evaluates appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</p></li><li><p>Analyzes data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making. </p></li><li><p>Prepares 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>To be 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>This role might be for you if you can/have:</strong> ​ ​</p><ul><li><p>Strong interest and motivation in exploring existing clinical trial data for post-hoc analysis and innovative ideas investigations</p></li><li><p>Experience with designing clinical trials especially observational types of studies, and Bayesian methods, machine learning techniques and causal inference methods</p></li><li><p>Exposure to Dermatology/Respiratory study endpoints and analysis techniques </p></li><li><p>Strong communication skills to interpret, explain, and discuss results of complex statistical concepts and analyses to both technical and non-technical audiences.</p></li><li><p>Desire to present and share results with internal and external stakeholders and co-author publications, as well as present at statistical/medical congresses </p></li><li><p>Experience with providing scientific/statistical input into study design, formulating novel problem-solving methods and independently developing the statistical analysis plan to implement those solutions.</p></li><li><p>Experience of authoring Statistical Analysis Plans (SAP) and Protocols </p></li><li><p>Experience with innovative ways to generate tables, listings, and figures for external communication use in publications/presentations and for internal purposes.</p></li><li><p>Ability to translate and apply relevant innovative statistical methodology to everyday work.</p></li><li><p>Experience of educating and disseminating knowledge throughout the organization for areas within the expertise of medical affairs.</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 >4 years’ experience in the pharmaceutical industry, or MS degree in statistics/biostatistics with >9 years’ experience. </p></li><li><p>Knowledge of drug life cycle management and strategies is preferred; knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies is a plus.</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>Be able to prioritize with multiple priorities and thrive in multitask type of environment</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Ability to write code in statistical software (i.e. SAS, R, Python) is required. </p></li></ul><p>#GDBDMJobs</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 19:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Scientist, Biologics Characterization]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45916]]></requisitionid>
    <referencenumber><![CDATA[R45916]]></referencenumber>
    <apijobid><![CDATA[r45916]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45916/sr-scientist-biologics-characterization/]]></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><br>Regeneron’s Product Biochemistry in Tarrytown, NY is seeking a motivated and innovative Senior Scientist to drive late-stage development (Phase II through commercialization) of biologics. You will develop and deploy analytical methods and purification strategies, enrich and characterize product variants, and help onboard new technologies that deepen product understanding and improve processes across the pipeline. This role is for you if you are scientifically creative, hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment.<br><br> </p><h3>Key Responsibilities:</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>Author high-quality technical documents (protocols, reports, memos) and contribute to regulatory sections and publications. Ensure timely documentation of experiments following established SOPs and guidelines.</li><li>Maintain instruments, troubleshoot issues, and improve lab/data workflows within your area of expertise. Adhere to procedures, guidance, and best practices to ensure lab safety.</li></ul><ul><li>Proactively identify process improvement opportunities across Product Biochemistry and Regeneron and help drive implementation.</li></ul><br><h3>A Typical Day in the Role Might Look Like:</h3><ul><li>Design and execute experiments to enrich, purify, and characterize size/charge variants, complexes, and high-concentration formulations.</li><li>Integrate learnings from internal data and external literature to make science-based study design recommendations.</li><li>Documents experiments, results and findings in electronic laboratory notebook; presents work at group and department meetings; contributes to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication.</li><li>Lead or participate in technology initiatives and continuous improvement projects; may also mentor and guide junior analysts in a matrix-based environment.</li><li>Maintain instruments, troubleshoot instrumental/experimental problems, and order/maintain supplies.</li></ul><h3>This Role Might Be For You If:</h3><ul><li>Possess strong lab skills in protein separation, purification, and tangential flow filtration (TFF). Possess skills in protein/product identification using mass spectrometry.</li><li>Thrive in a fast-paced, team environment and can also work independently across multiple projects.</li><li>Demonstrate initiative, calculated risk-taking, and a passion for innovation and continuous improvement.</li><li>Communicate clearly, manage projects effectively, and solve complex problems with data-driven rigor.</li><li>Mentor others and contribute to a safe, efficient, and inclusive lab environment.</li></ul><p>This role requires a BS/MS/Ph.D. in Biochemistry/Biophysics, or related field plus 8-10 yrs+ (BS/MS) or 0-2 yrs+ of proven experience (Ph.D.). Technical proficiency in automated FPLC and/or HPLC (SEC, IEX, affinity), electrophoresis (capillary or microchip, SDS-PAGE, western blots), spectroscopy and light scattering is recommended. A fundamental understanding of protein structure/function, mass spectrometry, and immunology/immunogenicity preferred. Preference will be given to candidates who have experience working in the biopharmaceutical industry. Excellent oral and written communication skills and evidence of teamwork are required. This role is fully onsite.</p><p>The ideal candidate must have strong initiative to complete tasks, learn new technologies, and demonstrate a commitment to continuous learning. This role requires the ability to manage multiple priorities in a fast‑moving R&D environment, operate effectively both independently and within a collaborative team environment, and communicate clearly, transparently, and in a timely manner with key stakeholders.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Data Science]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46197]]></requisitionid>
    <referencenumber><![CDATA[R46197]]></referencenumber>
    <apijobid><![CDATA[r46197]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46197/process-development-engineer-iii-data-science/]]></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>Regeneron’s Data Enablement and Analytics (DEA) team within Preclinical Manufacturing and Process Development (PMPD) is seeking a Machine Learning Engineer to develop, build and deploy analyses and machine learning models that support bioprocess development. This role is ideal for a data scientist with a strong foundation in chemical or biomedical engineering and a passion for building impactful solutions in close collaboration with scientists and process engineers.</p><p>You will work at the intersection of software engineering, data science, and bioprocess domain expertise—developing models that will be put into action within PMPD’s laboratory and manufacturing operations. You will mentor and coordinate citizen data scientists. Your work will streamline workflows, enable automation, and accelerate decision-making across PMPD.</p><h3>A Typical Day in the Role Might Look Like:</h3><ul><li><p>Partner closely with scientists, engineers, and analysts to understand bioprocess workflows and identify high‑impact data science opportunities.</p></li><li><p>Acquire, clean, and structure complex datasets to enable scalable, repeatable analyses.</p></li><li><p>Design, develop, and apply advanced analytics and machine learning models to drive data‑informed decision‑making.</p></li><li><p>Deploy models into production environments, enabling automated and autonomous operations where appropriate.</p></li><li><p>Lead, mentor, and coordinate citizen data scientists on critical initiatives across PMPD</p></li><li><p>Enhance, maintain, and extend existing analytics tools and platforms to support new use cases and evolving business needs.</p></li><li><p>Contribute as an active member of Agile teams within a Scaled Agile Framework, supporting planning, delivery, and continuous improvement.</p></li><li><p>Continuously evaluate emerging technologies and methodologies to strengthen data science capabilities within the organization</p></li></ul><h3>What You Bring</h3><ul><li><p>Bachelor’s or Master’s degree in Chemical Engineering, Biomedical Engineering, or a related discipline. 5-7 years of experience in bioprocess development, pharmaceutical manufacturing, or a closely related domain.</p></li><li><p>Demonstrated ability to apply machine learning and predictive analytics to complex, real‑world problems.</p></li><li><p>Strong programming skills in Python and SQL, with a solid understanding of data modeling and database design.</p></li><li><p>Experience working in Linux/Unix environments and using Git for version control and collaboration.</p></li><li><p>Excellent communication skills and a collaborative mindset, with the ability to partner effectively with scientists, engineers and analysts, while mentoring citizen data scientists.</p></li><li><p>Familiarity with DevOps and deployment technologies such as Kubernetes, NixOS, and Jenkins.</p></li><li><p>Experience with Operational Technology and analytics platforms (e.g., PI Historian, OPC, MQTT, Dataiku, Seeq) is a plus.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonary-Brooklyn, NY]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46137]]></requisitionid>
    <referencenumber><![CDATA[R46137]]></referencenumber>
    <apijobid><![CDATA[r46137]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46137/medical-specialist-i-pulmonary-brooklyn-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Brooklyn]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Brooklyn, NY</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>As a Medical Specialist, a typical day might include the following:</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 may be for you if you:</strong></p><ul><li><p>Are confident in demonstrating strong and consistent sales performance that exceeds expectations related to goals</p></li><li><p>Are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>Can demonstrate a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>Collaborate effectively with internal and external partners</p></li><li><p>Share a passion and learning interest in science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li></ul><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. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. 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. Ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 14:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Scientist, Product Biochemistry]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46115]]></requisitionid>
    <referencenumber><![CDATA[R46115]]></referencenumber>
    <apijobid><![CDATA[r46115]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46115/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>Summary</p><p>Our Product Biochemistry team is seeking a highly motivated <strong>Associate Scientist </strong>to join our growing team. A successful candidate will be responsible for performing protein purification, modification as well as providing in-depth characterization of therapeutic proteins to support research, pre-clinical and clinical assays. In this exciting role you will be part of method development and technology innovation efforts aimed to improve our understanding of biotherapeutic proteins/gene therapy reagents on a capillary based western systems.</p><p><strong> </strong></p><p><strong>A typical day as a Associate Scientist looks like:</strong></p><ul><li><p>Conducts biochemical and biophysical characterization experiments and analyze data to elucidate quality attributes of protein and gene therapy candidates</p></li><li><p>Develop methods/technologies to support both upstream and downstream functional groups</p></li><li><p>Perform protein purification and modification (labeling) as required to support therapeutic pre-clinical assay development and release testing</p></li><li><p>Document all analytical work in electronic laboratory notebook (ELN) according to a defined protocol accurately</p></li><li><p>Communicate any findings to supervisor</p></li><li><p>Summarize results in a concise format to support presentations and regulatory documents</p></li><li><p>Present findings at group, departmental, and cross-functional meetings</p></li><li><p>Maintain and troubleshoot essential instruments in lab</p></li></ul><p><strong> </strong></p><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Experienced in the general operations of a laboratory and able to manage and organize data with manager’s supervision. </p></li><li><p>Fundamental technical competencies in key analytical protein methodologies such as Size Exclusion Chromatography (SEC), UV-Vis spectrophotometry, SDS-PAGE, Western blotting, CE-SDS, protein purification and basic chemistry skills as applied toward protein modifications.</p></li><li><p>Experience on capillary electrophoresis is a plus.</p></li><li><p>Strong organizational skills and ability to prioritize multiple tasks are required. Deep understanding of biophysical/biochemical characterization of proteins, experience on analytical method development is desirable.</p></li></ul><p><strong> </strong></p><p><strong>In order to be considered qualified for this role, </strong>you must have a either a Masters or Bachelors degree in Biochemistry, Biophysical Chemistry, Biomedical engineering or related field and a minimum of 0-2 years of relevant post-degree laboratory experience with an emphasis on protein characterization and conjugation.</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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 21:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Quality Control Scientist (Chemistry)]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46048]]></requisitionid>
    <referencenumber><![CDATA[R46048]]></referencenumber>
    <apijobid><![CDATA[r46048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46048/sr-quality-control-scientist-chemistry/]]></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 looking for a Sr Quality Control Scientist in the Technical Resources Department. This position performs assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.</p><p>As a Sr QC Scientist for Chemistry in the Technical Resources Department, a typical day might include the following:</p><ul><li><p>Performs assay development/validation for QC.</p></li><li><p>Reviews new test procedures and assays.</p></li><li><p>Evaluates and bring in new methodologies/techniques when needed.</p></li><li><p>Facilitate assay transfer from R&D and to business partners</p></li><li><p>Organize analytical assay transfer internally and externally.</p></li><li><p>Set product specification.</p></li><li><p>Participates in technical troubleshooting and problem investigation.</p></li><li><p>Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.</p></li><li><p>Participates in training programs for analysts.</p></li></ul><p>This job might be for you if:</p><ul><li><p>You have in-depth knowledge with HPLC based assays.</p></li><li><p>You like dealing with technical issues, troubleshooting, and constant change</p></li><li><p>You are a team player who can work with a variety of different people on different tasks</p></li><li><p>You have strong written and verbal communication skills</p></li><li><p>You enjoy mentoring and training others on systems, processes and problem solving</p></li><li><p>You enjoy working in a fast-paced environment and are flexible to changing requirements</p></li><li><p>You can take on new and sometimes ambiguous challenges and learn quickly</p></li></ul><p>To be considered for a Sr QC Scientist (Chemistry) Technical Resources role you must have a BS in Chemistry, Biochemistry, Biology, or a related field, and 6+ years of relevant experience. Higher level degree preferred.</p><p>Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred.</p><p>Level is determined based on experience relevant to the role.</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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Commercial Operations - Immunology DACH (f/m/d)]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45704]]></requisitionid>
    <referencenumber><![CDATA[R45704]]></referencenumber>
    <apijobid><![CDATA[r45704]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45704/senior-manager-commercial-operations-immunology-dach-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, as a Senior Manager Commercial Operations Immunology (m/f/d), you will have the opportunity to actively shape the future of our commercial processes and make a significant contribution to field force excellence. Become part of a dynamic team and use your analytical skills to support the Immunology and Inflammation teams in Germany, Austria, and Switzerland.</p><h3><strong>A typical day might include:</strong></h3><ul><li><p>Analyze and interpret sales data from various sources to identify trends and insights.</p></li><li><p>Create reports and dashboards for sales and management teams.</p></li><li><p>Manage and optimize Commercial Operations, including field force excellence and incentive compensation planning.</p></li><li><p>Develop and improve processes to increase efficiency and standardization.</p></li><li><p>Collaborate with management on strategic planning and derive data-based recommendations.</p></li><li><p>Train and support sales teams in the use of analytical tools and promote a data-driven culture.</p></li><li><p>Coordinate with co-commercialization partners regarding field force metrics.</p></li><li><p>Integrate and prepare data for visualizations and analyses.</p></li></ul><h3><strong>This role might be for you if:</strong></h3><ul><li><p>You have excellent knowledge of MS Excel and experience with BI tools such as Tableau, Veeva CRM, Salesforce or Power BI.</p></li><li><p>You have strong communication skills for presenting analytical results.</p></li><li><p>High attention to detail, analytical thinking, and enthusiasm for working with data.</p></li></ul><h3>To be considered:</h3><ul><li><p>Applicants should have a University degree in Business Administration, Economics, or a related field and at least 8 years of professional experience in Sales Operations, or Data Analytics, including at least 2 years in an analytical role.</p></li><li><p>Experience in biotech/pharma is desired.</p></li><li><p>Fluent German required, and strong English skills.</p></li><li><p>Project management experience is an advantage.</p></li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, In Vivo & In Vitro]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44341]]></requisitionid>
    <referencenumber><![CDATA[R44341]]></referencenumber>
    <apijobid><![CDATA[r44341]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44341/associate-scientist-in-vivo-in-vitro/]]></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 highly motivated and experienced Associate Scientist to join the Obesity, Metabolic and Muscle Diseases Group to support our discovery and development efforts pertaining to liver metabolism and metabolic diseases. </p><p><strong>As an Associate Scientist, a typical day may include: </strong></p><p>The individual will be responsible for the execution of in vitro and in vivo biological experiments necessary to develop cell-based and animal models for testing of experimental therapeutics and for mechanistic biology studies. The ideal candidate will have in-depth in vitro or in vivo technical expertise, be hardworking, flexible, innovative and able to function effectively in a fast-paced environment. They will also have excellent communication skills and be able to work well in a team.</p><p><strong>This role may be for you if you have:</strong></p><p>Strong in vitro and in vivo technical expertise is required. Specifically:</p><p>In vitro technical expertise including, but not limited to:<br>- Tissue culture, transfections <br>- Western blotting and ELISA </p><p>- Molecular biology techniques</p><p> In vivo technical expertise including, but not limited to:</p><p>- Mouse handling, injections (IP, SC, IV), blood and tissues collection</p><p>The candidate will also perform relevant data analysis and interpretation, collate data for presentations or reporting, and present data at group meetings.</p><p>The candidate will be responsible for maintaining accurate and complete laboratory records.</p><p><strong>To be considered for this role, you must have: </strong></p><ul></ul><p> minimum of a Bachelors degree + 2 + years experience or Masters 0-2 year,</p><ul><li>must have in vivo experience</li><li>must have in vitro experience</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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Oncology Marketing - Core Brand]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44200]]></requisitionid>
    <referencenumber><![CDATA[R44200]]></referencenumber>
    <apijobid><![CDATA[r44200]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44200/associate-director-oncology-marketing-core-brand/]]></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, Oncology Marketing – Core Brand is a key member of the Oncology Business Unit and reports directly to the Global Core Marketing Lead. This role is responsible for shaping and driving above-indication strategy, ensuring brand consistency and strategic cohesion across indications. The Associate Director partners closely with the indication teams to integrate priorities and enable aligned, high-impact execution across brand planning, congress strategy and execution, ad boards, and field meeting planning.</p><p><strong>A typical day may include the following:</strong></p><ul><li>Leading the Global brand planning process by refining the framework and setting up a plan that ensures timely and successful delivery of the strategic plan, tactical plan, and finances integrating global regional and local plans.</li><li>Leading the franchise congress strategy which includes the execution of key congresses, identifying key promotional opportunities, setting measurement plans, and effectively leading cross-functional teams with multiple internal and external partners.</li><li>Driving the strategic vision for national sales meetings. Work in close collaboration with sales leadership, commercial operations, internal partners and production companies.</li><li>Spearheading the development of the Annual Advisory Board Plan [AABP] with partnership with medical counterparts. Effectively drive the process forward to ensure timely leadership review and approval of the AABP every year.</li><li>Developing customer-focused and differentiated marketing materials for target audiences including approval through RC.</li></ul><p><strong>To be considered, you must possess:</strong></p><ul><li>Bachelor's degree and 5+ years of progressive experience in HCP Marketing, Plan of Action Meetings, Congress Management, and Strategic Brand Planning. Oncology and pharmaceutical sales experience a plus.</li><li>Experience in budget management and working with creative agencies and regulatory/legal review processes (RC).</li><li>Emotional intelligence, including poise and business maturity to manage confidential information and gain credibility with senior leaders.</li><li>Ability to effectively navigate ambiguity (high learning agility) and develop paths forward to successfully complete initiatives and get results.</li><li>Ability to work on multiple projects with a wide range of constituents, with a proven track record of being able to collaborate, prioritize, and achieve successful outcomes.</li><li>Onsite role requiring 4 days per week in the Sleepy Hollow office. Must be willing to travel 35-40% (including weekend travel as needed).</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 06:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Martech & Field Enablement Lead]]></title>
    <date><![CDATA[Sun, 29 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46228]]></requisitionid>
    <referencenumber><![CDATA[R46228]]></referencenumber>
    <apijobid><![CDATA[r46228]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46228/executive-director-commercial-martech-field-enablement-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>We are seeking a transformative and strategic senior leader with a wealth of diverse experience to work in close collaboration with BU SVPs and VPs and their leadership teams to develop and lead the vision, strategy, and execution for field-facing colleague engagement and operations to enable exceptional colleague and customer experiences.</p><p>This individual will be responsible for significantly elevating the enablement of customer-facing teams and a critical focus of this role is modernizing systems, capabilities and effectiveness through MarTech (Marketing Technology) solutions, including CRM systems, AI-driven tools, and digital engagement platforms.</p><p>This leader will ensure that technology investments are aligned with business priorities, enhance field enablement, and deliver measurable outcomes. The role requires close collaboration with not only Business Unit leaders but also with enablement leaders such as IT, SI&A, and Market Access. Responsibilities will also be to design and oversee institution of new programs and offerings as well as the development and implication of required behavior change solutions to ensure transformations are adopted, effectively integrated into work flow, and optimized to deliver continuous improvement in service of the business.</p><br><h3><strong>A Typical Day Might Look Like This:</strong></h3><br><p>MarTech Strategy & Enablement:</p><ul><li>Develop and implement a comprehensive <strong>MarTech strategy</strong> to optimize CRM systems, AI-driven initiatives, and digital engagement platforms for field enablement.</li><li>Lead the implementation and integration of CRM technology to support pre-call planning, next-best-action recommendations, and first-call resolution (FCR). Role will also require designing well-rounded engagement solutions to harness entire x functional customer facing team</li><li>Prioritize technology investments based on business needs, ensuring alignment with BU priorities and organizational goals.</li><li>Oversee enablement for AI-driven solutions that enhance customer engagement, improve field productivity, and deliver actionable insights.</li><li>Collaborate with IT, SI&A, and commercial operations teams to ensure seamless integration of tools and technologies into field workflows.</li><li>Drive adoption and utilization of MarTech solutions across field teams, ensuring measurable improvements in engagement effectiveness and operational efficiency.</li><li>Partner with training teams to ensure field colleagues are equipped to harness MarTech tools effectively in their daily activities.</li></ul><p>Strategy & Vision:</p><ul><li>Define and communicate the long-term vision for field enablement and engagement strategy across businesses, ensuring alignment with each BU</li><li>Develop a well-rounded strategy for how field-facing colleagues engage customers (HCPs, institutions, payers, and how the organization supports them through tools, training, CRM, and processes.)</li><li>Translate vision into a prioritized roadmap, outlining capabilities, tools, processes, and metrics to optimize over the next 1-3 years.</li><li>Collaborate with BU and enablement leaders to identify business priorities and ensure enablement initiatives address specific needs while maintaining appropriate consistency.</li><li>Design, implement and optimize system for ongoing behavior change to ensure effective adoption and utilization of solutions</li></ul><p>Field Enablement & Excellence:</p><ul><li>Lead enablement initiatives for customer-facing colleagues, ensuring they have the tools, processes, and support to deliver differentiated engagements.</li><li>Partner closely with training teams to design and implement programs that address role-specific needs and capabilities, ensuring effective adoption and readiness.</li><li>Define metrics and success criteria and oversee and monitor performance of new solutions</li><li>Drive continuous improvement by identifying gaps in performance or engagement quality and leading interventions such as training (in partnership with training team), process redesign, or technology upgrades.</li><li>Develop operational standards and make recommendations to optimize customer engagements</li></ul><p>Engagement Strategy:</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>Support the voice of the customer in the organization, ensuring that we understand the needs of HCPs, institutions, payers, and other pharma customers so they can receive meaningful, consistent, high-quality engagements.</li><li>Partner with commercial, medical, marketing, and enablement teams to ensure a seamless, supportive, and compliant engagement journey that differentiates the company from competitors.</li><li>Lead initiatives to design or optimize engagement models, feedback loops, and metrics.</li><li>Ensure governance and compliance appropriate to the pharmaceutical industry, including adherence to promotional regulations, data privacy standards, and HCP engagement codes.</li><li>Oversee the end-to-end healthcare provider (HCP) experience, ensuring interactions are seamless, supportive, and impactful.</li></ul><p>Cross-Functional Leadership & Execution:</p><ul><li>Act as a senior partner across the business, collaborating with leaders in Marketing, Sales, Medical Affairs, Access, Commercial Operations, Compliance, IT/Analytics, and others to ensure alignment of enablement and engagement strategy with business plans.</li><li>Lead and develop a small and high-performing team, fostering a culture of excellence, accountability, and continuous learning.</li><li>Oversee budgeting, resource allocation, vendor/agency relationships, and execution of major projects and initiatives.</li></ul><h3><strong>This role may be for you if</strong><strong>:</strong></h3><ul><li>You have expertise in CRM technologies, digital engagement solutions, and data/analytics to drive enablement effectiveness.</li><li>You are an exceptional cross-functional collaboration skills, influencing at senior levels, and strong communication and executive presence.</li><li>You demonstrated ability to lead teams, manage change, optimize processes, scale operations, and thrive in a dynamic, regulated environment.</li></ul><p>To be considered you have a Bachelor’s degree required; MBA or advanced degree preferred. You bring at least 15 years of dynamic experience in the pharmaceutical or biotech industry, with significant leadership experience in commercial, field, enablement, or engagement roles. IT experience, either in role or as part of cross functional team, preferred. You bring a proven track record of developing and implementing enablement, field excellence, and MarTech strategies, particularly CRM and AI-driven solutions, in pharma or life sciences (or analogous regulated industries).</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 30 Mar 2026 07:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology (Iowa/Western Illinois)]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43133]]></requisitionid>
    <referencenumber><![CDATA[R43133]]></referencenumber>
    <apijobid><![CDATA[r43133]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43133/medical-specialist-ii-ophthalmology-iowawestern-illinois/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Peoria]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Territory: Iowa/Western Illinois</strong></h3><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.<br> </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>$152,300.00 - $195,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Program Management Process and Standards]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46277]]></requisitionid>
    <referencenumber><![CDATA[R46277]]></referencenumber>
    <apijobid><![CDATA[r46277]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46277/director-program-management-process-and-standards/]]></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>The <strong>Director, Development Program Operations</strong> will have a leadership role in the building and optimization of the Strategic Program Team’s (SPTs) operating model and Development capabilities (processes, tools, services) that contribute to the company’s performance and operational excellence. Under this role’s leadership, the team is accountable for generating actionable insights and recommendations to senior leadership to drive how we scale our operating model, for example our team membership composition, roles/responsibilities, deliverables.</p><p>Additionally, this role is responsible for designing, building and managing cross-functional business-critical initiatives that drive the acceleration of portfolio delivery. These initiatives require strong matrix leaders with drug development and business acumen and are passionate about applying robust strategic change execution methods and best practices. The role will need to anticipate business needs through strategic planning and trend analysis and with alignment of key stakeholders across Development with interfaces in Research, Manufacturing and Commercial. Operates with a continuous improvement mindset to enable cross functional operational efficiencies.</p><p>This role is a hands-on contributor and people manager responsible to build relationships at all levels of the organization in order to solicit and action stakeholder input regarding the SPT operating model. This role will navigate the fast-paced and agile environment of Regeneron in a collaborative and innovative manner.</p><p><em>***Note: this role requires 4-days onsite in either Tarrytown, NY or Warren, NJ and is not eligible fully remote. </em></p><p><strong>A typical day in this role looks like: </strong></p><ul><li>Identify, create and drive strategic initiatives related to the DPM and SPT operating model with direct impact to drive Development portfolio and pipeline </li><li>Partner with Program and Portfolio Management (PPM) Leadership Team and Development functional areas to monitor and measure implementation impacts and take action when needed </li><li>Develop, maintain and implement project/program management methodology, including processes, tools, metrics and policies to ensure efficiency, quality and business success </li><li>Drive consistency and standardization across program strategy execution and ensures compliance to the application of these execution methodologies and standards </li><li>Design and implement the operating cadence, including running coordination meetings, project updates and overall oversight of projects </li><li>Work with Development and PPM Leadership to define innovative operational Key Performance Indicators (KPIs) for the projects and services delivered, tracking these KPIs across the department and projects to ensure goals are consistently achieved </li><li>Build strong, interdependent partnerships and manages the communication effectively with functional area heads in Development, key stakeholders in Research, Commercial and Manufacturing </li><li>Responsible for the coaching and development of department members as well as ensuring that the organizational strategy delivers the skills, capabilities and processes that enable portfolio delivery are present in his/her team </li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Significant experience in the biotechnology or pharmaceutical industry with a strong understanding of drug development activities in context of line functions and project teams </li><li>Consulting experience and experience with developing a Project Management Office (PMO) is desirable </li><li>Proven experience in a similar role; understanding of Operational Excellence, Six Sigma/LEAN and business process management preferred </li><li>Proven leadership skills with the ability to innovate and drive framework and change in a matrixed environment, amidst ambiguity </li><li>Lead the department with a customer-first demeanor </li><li>Strong analytical, problem-solving and strategic thinking abilities </li><li>Strong organizational and multitasking abilities, overseeing multiple projects simultaneously </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 information and insights effectively </li><li>Experience in building and leading high performing teams and driving cross-functional initiatives </li><li>IT proficiency with MS software and project management tools, analytics and visual reporting applications (e.g. SharePoint, MS Project, PowerPoint, Word, Excel, PowerBI, etc) </li><li>Ability to travel (<10%) </li></ul><p><strong>In order to be considered qualified</strong>, a minimum of a Bachelor’s degree (Bachelor of Science) and 12+ years industry experience with a minimum of 5+ years in project management experience required. MBA preferred. </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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 17:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Corporate Counsel - Privacy / Transactions]]></title>
    <date><![CDATA[Tue, 23 Sep 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R40035]]></requisitionid>
    <referencenumber><![CDATA[R40035]]></referencenumber>
    <apijobid><![CDATA[r40035]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r40035/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[<p>Regeneron Pharmaceuticals is seeking a highly experienced transactions attorney for a pivotal role to serve as the 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 involves drafting, reviewing, negotiating, and providing strategic counsel on a diverse portfolio of agreements across our innovative business units.</p><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, 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><em><strong>The role will be based onsite at our offices in Cambridge, MA or Sleepy Hollow, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><br>A typical day might include the following:</p><ul><li>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.</li><li>Maintaining subject matter expertise in data privacy laws and the Regeneron privacy policies and advising Transaction Law colleagues and clients on developments of importance.</li><li>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.</li><li>Responding to U.S. and ex-U.S. contracting questions.</li><li>Managing updates to group’s data privacy contracting playbook.</li><li>Creating data privacy contracting tools and training materials.</li><li>Managing office hours with internal business partners.</li><li>Developing and training on privacy contracting tools and requirements.</li><li>Acting as liaison for the Transactions Law Group with the Data Privacy Office on data privacy policy questions and approaches.</li></ul><p><br>This role might be for you if:</p><ul><li>You have the ability to work independently, while meeting aggressive deadlines and juggling multiple matters.</li><li>You are able to maintain an objective perspective while developing and maintaining strong partnerships with key stakeholder / client organizations and protecting Regeneron’s interests.</li><li>You can work effectively and professionally with colleagues and clients at all levels of the organization and in a collaborative, team-oriented environment.</li><li>You have the ability to effectively convey to, and respond to questions from, colleagues and key stakeholders, on data privacy law concepts. </li></ul><p><br>To be considered for this position you must possess a JD with excellent law school credentials. Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel is preferred. At least 7 years of legal experience at a law firm and/or in-house, with some biotech/pharmaceutical and/or health care experience is preferred. Solid understanding of contracts and related law. Experience with contracts involving data privacy and intellectual property. You should also have a high level of business acumen, excellent contract drafting and negotiation proficiency, exceptional oral and written communication skills and interpersonal and conflict resolution capability.</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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$202,000.00 - $336,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 15:56:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, GxP Enterprise Architecture]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44202]]></requisitionid>
    <referencenumber><![CDATA[R44202]]></referencenumber>
    <apijobid><![CDATA[r44202]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44202/director-gxp-enterprise-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[<p>The Director, GxP Enterprise Architecture leads the IT architecture practice for manufacturing and operations (e.g., manufacturing, QA, QC, process sciences, supply chain). This role defines technology strategy and standards, governs platform decisions, and ensures solutions meet GxP and data integrity requirements while advancing business capabilities and long-term platform health.</p><p>As a Director, GxP Enterprise Architecture, a typical day might include the following:</p><ul><li>Define and evolve EA governance, standards, reference architectures, and reusable patterns across application, integration, data, and infrastructure.</li><li>Own the multi-year technology roadmap aligned to business capability priorities and lifecycle plans.</li><li>Lead architecture reviews, maintain the application portfolio, and manage technical debt and end‑of‑life risk.</li><li>Ensure alignment with enterprise-wide architecture, avoid redundant platform investments while identifying capability gaps.</li><li>Translate market trends (ERP, MES, LIMS, QMS, data, cloud, integration) into actionable guidance and adoption plans.</li><li>Manage business strategy enablement options, and trade-offs met by technology with business leaders.</li><li>Collaborate with corporate IT's Architecture team to ensure architectural standards are in place and enforced.</li><li>Ensure Architecture Standards are aligned with 21 CFR Part 11, Annex 11, data integrity, and CSV/CSA requirements</li><li>Produce and maintain target-state architectures, capability maps, roadmaps, solution blueprints, integration diagrams, and ADRs.</li></ul><p>This role may be for you if you have knowledge in:</p><ul><li>GMP systems landscape: ERP (e.g., Oracle EBS, Oracle Fusion), MES, LIMS/ELN, QMS, WMS, EDMS; familiarity with SCADA/DCS and shop-floor integration.</li><li>Integration patterns and platforms: APIs, event-driven architecture, EDI, ETL/ELT; iPaaS/ESB (e.g., MuleSoft, Boomi), OPC UA; canonical data models.</li><li>Data and analytics: data lakehouse (e.g., Snowflake, Databricks), MDM, data governance, metadata lineage, BI platforms; ISA-95 data layers.</li><li>Cloud and infrastructure: AWS/Azure services, hybrid architectures, VPC/VNet design, containerization (Kubernetes), IaC (Terraform), CI/CD, microservices.</li><li>Security and compliance: identity and access management (Azure AD), segregation of duties, network segmentation/OT boundary patterns, NIST/ISO 27001 controls, backup/DR.</li><li>Architecture practice: TOGAF/ArchiMate, modeling tools (e.g., LeanIX, Lucidchart), solution blueprinting, ADRs, and traceability for audits.</li><li>SDLC and delivery: Agile/SAFe, DevOps in regulated environments, validation documentation (URS/FS/DS), risk-based CSA.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with 12 years of experience in a relevant industry or equivalent combination of education and experience. Biotechnology/Life Sciences industry experience, preferred.</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>$192,900.00 - $321,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 12:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs - Hematology - Ontario]]></title>
    <date><![CDATA[Thu, 13 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42140]]></requisitionid>
    <referencenumber><![CDATA[R42140]]></referencenumber>
    <apijobid><![CDATA[r42140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42140/senior-manager-field-medical-affairs-hematology-ontario/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p></div><div><p>We are seeking a <strong>Senior Manager, Field Medical Affairs – Hematology</strong> to join our team and strengthen our partnerships with experts in hematologic malignancies. In this role, you will engage with key opinion leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. You’ll play a meaningful role in the understanding of Regeneron’s therapies, supporting clinical development and investigator-initiated research, and contributing to impactful new therapies. </p></div><div><p>We are looking for our next team member to join our passionate & dedicated Medical Affairs team in Canada. This is a remote, field-based role located in the Greater Toronto Area, Ontario, Canada.</p></div><div><p><strong>Senior Manager, Field Medical Affairs, Hematology</strong></p><p><strong>Greater Toronto Area, Ontario, Canada</strong></p></div><div><p><strong>A Typical Day:</strong> </p></div><div><ul><li><p>Building and maintaining relationships with KOLs in malignant hematology. </p></li></ul></div><div><ul><li><p>Acting as a primary clinical/scientific contact for HCPs and investigators. </p></li></ul></div><div><ul><li><p>Generating medical insights to advise strategy and development plans. </p></li></ul></div><div><ul><li><p>Supporting clinical trial execution by identifying investigators and trial sites. </p></li></ul></div><div><ul><li><p>Collaborating on abstracts, posters, and manuscripts to communicate data. </p></li></ul></div><div><ul><li><p>Contributing to investigator-initiated study programs and research collaborations. </p></li></ul></div><div><ul><li><p>Attending medical congresses to support scientific exchange. </p></li></ul></div><div><ul><li><p>Partnering cross-functionally with Medical Affairs, Commercial, and Market Access. </p></li></ul></div><div><p><strong>This Role May Be For You:</strong> </p></div><div><ul><li><p>You thrive on scientific exchange and are confident discussing complex data with KOLs. </p></li></ul></div><div><ul><li><p>You have established background in hematology and understand the oncology landscape. </p></li></ul></div><div><ul><li><p>You enjoy balancing independent field work with cross-functional collaboration. </p></li></ul></div><div><ul><li><p>You adapt easily to changing priorities and field-based challenges. </p></li></ul></div><div><ul><li><p>You are motivated by opportunities to contribute to country readiness and new research. </p></li></ul></div></div><div><div><ul><li><p>You value compliance and integrity while working with investigators and partners. </p></li></ul></div><div><ul><li><p>You are comfortable with frequent travel and engaging in high-level conversations. </p></li></ul></div><div></div><div></div><div><p>To be considered, you should bring at least 5 years of field medical or medical manager experience in biotech or pharma, with a strong background in hematology. Knowledge of malignant hematology is required, and experience in lymphoma or multiple myeloma is preferred. Country readiness experience and established KOL relationships are highly valued. You should also have solid knowledge of treatment guidelines, clinical research, and Canadian regulations. Strong communication, organizational skills, and the ability to travel up to 70% are essential. </p></div></div><ul></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences, Hematology]]></title>
    <date><![CDATA[Wed, 29 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43418]]></requisitionid>
    <referencenumber><![CDATA[R43418]]></referencenumber>
    <apijobid><![CDATA[r43418]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43418/medical-director-clinical-sciences-hematology/]]></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 Medical Director, Clinical Sciences functions as clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), under leadership of Program Lead Medical Director (Program Lead MD) or Sr. Medical Director.</p><p>A day in the life may include the following responsibilities:</p><ul><li><p>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program with minimal supervision from Program Lead MD. </p></li><li><p>Manages all operational aspects and drives execution of the section of the clinical program in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates.</p></li><li><p>Supports Program Lead MD (and/or Sr. MD) and frequently lead interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards.</p></li><li><p>Serves occasionally as member for Global Clinical Development training programs, author or reviewer for clinical SOPs and may contribute to GCD strategy by serving on taskforces or other panels.</p></li></ul><p>This job may be for you if:</p><p>· You are passionate about impacting entire populations of patients</p><p>· You want to develop innovative new therapies</p><p>· You enjoy collaborating with team members towards a common goal.</p><p>In order to be considered for this position, you must have an MD or equivalent, ideally with Hematology Oncology fellowship training. More than 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV is strongly preferred. Medical/scientific expertise in disease area of assigned program is preferable. </p><p>#MDJOBS #heme</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>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation System Administrator]]></title>
    <date><![CDATA[Sun, 21 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43987]]></requisitionid>
    <referencenumber><![CDATA[R43987]]></referencenumber>
    <apijobid><![CDATA[r43987]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43987/automation-system-administrator/]]></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>As an Automation System Administrator, you will be embedded in a tight-knit team responsible for administration of automated/computerized system software and firmware to meet cGMP and policy requirements. In this critical role our team specifies and maintains software configuration for biopharmaceutical process, monitoring, and testing systems. This involves evaluation of new software for functional equivalence, validation activities to demonstrate suitability of software/process and maintaining the qualified state of systems throughout their lifecycle through change control.</p><p>In this role, a typical day might include:</p><ul><li>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</li><li>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</li><li>Utilizing configuration management and recipe/method management.</li><li>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</li><li>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</li><li>Conducting system integration with existing systems (e.g. LIMS, Historian).</li><li>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and/or design specifications, test plans, technical evaluation, and quality risk assessments.</li><li>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</li><li>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</li><li>Leading aspects of the work for contractors and providing guidance as applicable.</li></ul><p>This role might be for you if you:</p><ul><li>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</li><li>Have interest in manufacturing process within a regulated technical environment.</li><li>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</li><li>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</li><li>Understand process control systems and product release testing systems.</li><li>Are familiar with regulatory and quality policies, procedures, documentation methods.</li><li>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</li><li>Enjoy project management and have strong organizational skills.</li><li>Are motivated to participate in continuous process improvement.</li></ul><p>Applicants ideally should have a BS/BA in Science, Engineering or related field and the following minimum relevant experience for each level:</p><ul><li>Automation System Administrator: 2+ years</li><li>Senior Automation System Administrator: 5+ years</li></ul><p>Equivalent combination of education and experience may be considered. Level will be determined based on qualifications relevant to the role.</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>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Drug Supply & Logistics]]></title>
    <date><![CDATA[Mon, 12 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44560]]></requisitionid>
    <referencenumber><![CDATA[R44560]]></referencenumber>
    <apijobid><![CDATA[r44560]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44560/senior-manager-clinical-drug-supply-logistics/]]></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>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><p><strong>Supply Planning</strong></p><ul><li>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.</li><li>Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical development plan.</li><li>Works with clinical drug supply management to determine resourcing needs.</li><li>Provides input to the development of IP-related study documents including protocols, study and pharmacy manuals.</li><li>Responsible for working within established timelines of investigational product manufacturing, labeling, release, distribution and return/destruction, and/or helping to establish these timelines. </li></ul><p><strong>Inventory tracking</strong></p><ul><li>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.</li></ul><p><strong>Shipments</strong></p><ul><li>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.</li></ul><p><strong>IVRS</strong></p><ul><li>Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS.</li><li>Works with cross-functional teams to develop specifications and support user testing of IRT systems provided by 3rd party vendors.</li><li>Leads effort for clinical supply management functionality.</li><li>Monitors and manages clinical supply activities through IRT from study start-up through study closure.</li></ul><p><strong>Returns & Destruction</strong></p><ul><li>Develops strategy and oversees drug return and destruction activities.</li></ul><p><strong>Expiry Management</strong></p><ul><li>Develops resupply strategies based on stability and shelf-life of clinical supplies.</li><li>Monitors IP expiry data and informs Clinical Supply team and Clinical Trial teams of pending IP expiry.</li></ul><p><strong>Ancillary & Comparator Supplies</strong></p><ul><li>Coordinates with other functional areas, including Regulatory, Medical Director, Forecasting & Planning, and IOPS to define ancillary and/or comparator supply strategy.</li><li>Develops plans for supplying clinical study sites with ancillary and/or comparator supplies, either through in-house initiated supply or working with supply vendors.</li></ul><p><strong>Documentation</strong></p><ul><li>Provides input to drug kit randomization specifications and reviews and approves master kit lists.</li><li>Designs, reviews, and approves IP-related study tools (for clinical study teams and investigative site use), as needed.</li><li>Supports inspection team in preparation for and during regulatory agency inspection. May represent Clinical Drug Supply & Logistics during regulatory agency inspections.</li></ul><p><strong>Study Team Interaction</strong></p><ul><li>Represents Clinical Drug Supply & Logistics on cross-functional study team (s) and/or sub-team(s).</li><li>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.</li></ul><p><strong>Budget Management</strong></p><ul><li>Provides input into budgets, SoWs, contracts and timelines for IP-related services.</li><li>Creates RFPs, reviews quotes, and awards third-party vendors for distribution services.</li><li>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.</li></ul><p><strong>Vendor Management</strong></p><ul><li>Leads management of IP service vendors (performance, quality, timelines, deliverables, costs)</li><li>Participates in preparation of RFP, assumptions and SOW for CROs and IP services vendors (labeling, packaging, distribution; IVRS/IWRS)</li><li>Provides input, reviews, and approves vendor study specifications for IP-related activities.</li><li>Serves as point of escalation for vendor-related IP issues as they arise.</li><li>May require 25% travel</li></ul><p><strong>Staff Management</strong></p><ul><li>May supervise staff.</li><li>May mentor or coach junior Clinical Drug Supply & Logistics staff.</li></ul><p><strong>Process Initiatives</strong></p><ul><li>Develops and implements process initiatives in accordance with business needs.</li></ul><p><strong>Metrics</strong></p><ul><li>Tracks metrics related to drug supply processes and staff.</li></ul><p><strong>Training</strong></p><ul><li>Provides assistance in training and development as needed.</li></ul><p><strong>Reporting</strong></p><ul><li>Compiles and reports supply status to study teams and senior management</li></ul><p><strong>Problem solving</strong></p><ul><li>Applies knowledge of company policies and standard practices to resolve problems.</li></ul><p><strong>In order to be considered qualified for this role,</strong> a minimum of a Bachelor's degree and 8 years of relevant experience in the biotechnology/pharmaceutical industry, with 5 years minimum in clinical supply management. A Masters/MBA/PharmD with 5+ years of relevant industry experience is accepted.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 13 Jan 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences, MASH/Metabolism (Regeneron Genetics Medicine)]]></title>
    <date><![CDATA[Mon, 19 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44213]]></requisitionid>
    <referencenumber><![CDATA[R44213]]></referencenumber>
    <apijobid><![CDATA[r44213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44213/medical-director-clinical-sciences-mashmetabolism-regeneron-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>The Medical Director, Clinical Sciences, MASH/Metabolism works with their supervisor and other members of the cross-functional study team to author protocols and facilitate execution of study activities and data summarization. Takes lead on collaborations with discovery scientists and translational colleagues to understand current and emerging genetic targets across a variety of therapeutic areas and disease states including but not limited to MASH and metabolism, rare diseases, and others; provides input on potential disease areas/indications; and crafts clinical experiments that corroborate or inform the biology for decision-making purposes and enable clinical development programs.</p><p><strong>As a Medical Director, a typical day might include the following:</strong></p><p>• Leads the cross-functional study team to craft novel clinical development strategy for genetic medicines, including First in Human (FIH), Phase 2, and Phase 3 clinical trials</p><p>• Responsible for the relevance and accuracy of medical science underpinning of clinical study based on detailed scientific review and consultation</p><p>• Authors, reviews, and finalizes the medical and scientific portions of study strategies and clinical study protocols and amendments</p><p>• Authors, reviews, and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions</p><p>• Accountable for timely clinical trial execution, reviewing adverse events, monitoring patient health, and quality of results</p><p>• Analyzes the benefits and risk aspects of an assigned therapeutic candidate </p><p>• Ensures clinical team compliance with FDA, EMEA, ICH and GCP guidelines as well as SOPs regarding safety</p><p>• Authors clinical sections of communications/documentation for regulatory agencies and may participate in meetings as needed</p><p>• Conducts detailed literature reviews and analysis of development opportunities from mechanistic, pharmacological and clinical development perspectives</p><p><strong>This role may be for you if: </strong></p><p>• You want to make an impact delivering genetic medicines for patients with serious diseases</p><p>• You have specialist postgraduate clinical training and practice, and/or scientific research training and with a track record of success</p><p>• You demonstrate critical, science-to-medicine translational thinking skills and sound decision making</p><p>• You have the ability to work productively in a fast-paced collaborative working environment</p><p>To be considered for this role, you must have an M.D. Degree (M.D./Ph.D. Degree or prior research experience preferred). Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred. A minimum of 2-3 years of clinical practice or industry experience is preferred. This role requires a minimum of four days on-site weekly in Tarrytown, NY.</p><p>#MDJOBS, #MDJOBSCD</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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 20 Jan 2026 10:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney]]></title>
    <date><![CDATA[Tue, 20 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44376]]></requisitionid>
    <referencenumber><![CDATA[R44376]]></referencenumber>
    <apijobid><![CDATA[r44376]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>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.<br><br><strong>As a Director Patent Attorney, a typical day may include:</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>Assisting in litigation activities as needed</p></li><li><p>Supporting due diligence projects, agreements and other transactional work, administrative initiatives, and policy questions.</p></li></ul><p><strong>This role might be for you if you have experience:</strong></p><ul><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>To be considered for this position, you must possess</strong> a Ph.D. in the life sciences (e.g., biochemistry, molecular biology, cell biology, or related fields) is required with a Juris Doctorate from an accredited law school. 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); 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><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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 21 Jan 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Logistics Business Process Owner]]></title>
    <date><![CDATA[Wed, 28 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44187]]></requisitionid>
    <referencenumber><![CDATA[R44187]]></referencenumber>
    <apijobid><![CDATA[r44187]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44187/director-erp-logistics-business-process-owner/]]></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>The Director, ERP Logistics Business Process Owner will lead the transformation of logistics-related processes as part of our ERP Modernization Program. In this strategic role, you will define and optimize processes across Warehouse Management System (WMS), Transportation Management System (TMS), Global Trade Management (GTM), and inventory management. By collaborating with cross-functional teams, you will drive process standardization, support global adoption, and enable supply chain efficiency, operational excellence, and compliance. If you are passionate about logistics process design, change management, and delivering measurable results, this role offers an exciting opportunity to make a significant impact.</p><p>As the Director, ERP Logistics Business Process Owner a typical day might include the following:</p><ul><li>Defining and documenting future-state logistics processes (WMS, TMS, GTM, and inventory management) aligned with strategic business goals.</li><li>Collaborating with IT, Business Process Leads, and Program Delivery teams to ensure seamless integration of logistics processes into the ERP modernization initiative.</li><li>Partnering with business teams to analyze current workflows and identify opportunities for standardization and improvement.</li><li>Leading change management strategies to drive adoption of new logistics processes across global teams.</li><li>Resolving process-related challenges during implementation and post-deployment phases.</li><li>Facilitating workshops and meetings to gather input, align stakeholders, and address concerns.</li><li>Monitoring the effectiveness of logistics processes post-deployment and implementing continuous improvement initiatives.</li><li>Ensuring all processes comply with industry standards and regulatory requirements, including SOX and GxP.</li></ul><p>This Role May Be For You If</p><ul><li>You are a strategic thinker who thrives on solving complex logistics process challenges.</li><li>You enjoy collaborating across diverse functions and geographies to achieve shared goals.</li><li>You are passionate about driving change and inspiring teams to adopt new ways of working.</li><li>You have expertise in logistics process design, including WMS, TMS, GTM, and inventory management.</li><li>You are detail-oriented and excel at managing multiple initiatives simultaneously.</li><li>You value compliance and understand its critical role in logistics processes.</li><li>You are skilled at facilitating workshops and fostering stakeholder alignment.</li></ul><p>To qualify for this role, you must have a bachelor’s degree in Business, Supply Chain, Engineering, or a related field and</p><ul><li>Associate Director: 10+ years of experience in business process design and transformation within manufacturing or supply chain environments.</li><li>Director: 12+ years of experience in business process design and transformation within manufacturing or supply chain environments.</li><li>Senior Director: 15+ years of experience in business process design and transformation within manufacturing or supply chain environments.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Advanced degree and familiarity with ERP systems (e.g., Oracle, SAP) and logistics modules such as WMS, TMS, GTM, and inventory management is 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>$147,800.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 29 Jan 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Benefits]]></title>
    <date><![CDATA[Wed, 04 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44294]]></requisitionid>
    <referencenumber><![CDATA[R44294]]></referencenumber>
    <apijobid><![CDATA[r44294]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44294/senior-manager-benefits/]]></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 seeking an experienced and dynamic Senior Manager, Benefits to oversee the day-to-day operations of our U.S. employee benefits programs. This role involves managing a team of professionals, ensuring smooth execution of benefits-related activities, partnering with Human Resources Business Partners (HRBPs) and other HR Centers of Excellence (COE), and driving strategic initiatives to enhance employee satisfaction and organizational effectiveness. The ideal candidate will have strong leadership, organizational, and communication skills, coupled with deep expertise in employee benefits administration. This role will report to the Director Benefits. Travel to other NY offices approximately once a month is expected.</p><p><strong><em>This role could be based at either our Sleepy Hollow, NY or Rensselaer, NY </em><em>location </em><em>with a minimum of 4 days onsite required - this is not open to fully remote or hybrid work.</em></strong></p><p>The ideal candidate will have hands-on experience in administering employee benefit programs, with the ability to understand the end-to-end process. They will have the ability to understand complex benefit issues, how to navigate and bring to resolution.</p><ul><li>Experience administering a self-insured health plan including plan design and budgeting.</li><li>Good presentation skills. Putting together clear, professional presentations that can be delivered to employees new in their careers and to seasoned executives.</li><li>Ability to think through complex issues using foundational knowledge of legal requirements and previous experience; and ability to think outside of the obvious.</li></ul><p>Key Responsibilities: </p><p>Benefits Administration </p><ul><li>Oversee the day-to-day operations of employee benefits programs, including health plans and additional benefits.</li><li>Ensure timely enrollment, compliance, and accurate processing of benefits-related transactions.</li><li>Serve as the point of escalation for complex benefits issues and inquiries. </li></ul><p>Team Leadership </p><ul><li>Lead, mentor, and manage a team of benefits specialists, ensuring collaboration and high performance.</li><li>Provide coaching, training, and professional development opportunities to team members.</li><li>Foster a positive and inclusive team environment that encourages innovation and continuous improvement. </li></ul><p>Compliance and Reporting </p><ul><li>Ensure compliance with all federal, state, and local regulations related to employee benefits, such as ACA, ERISA, COBRA, and HIPAA. </li><li>Oversee preparation and submission of required reports and documentation to regulatory agencies. </li><li>Stay updated on changing laws and regulations, advising leadership on necessary adjustments, working with appropriate stakeholders. Update policies and procedures as needed. </li></ul><p>Vendor Management </p><ul><li>Manage relationships with benefits vendors and third-party administrators. </li><li>Negotiate contracts, monitor service levels, and evaluate vendor performance. </li><li>Attend regular meetings to receive updates, understand any current issues and opportunities that will deliver a better employee and administrator experience.</li></ul><p>Strategic Planning </p><ul><li>Collaborate with HR leadership to design and implement benefits strategies that align with organizational goals. </li><li>Analyze data and trends to identify opportunities for cost savings and program enhancements. </li><li>Champion initiatives that promote employee well-being and engagement. </li></ul><p>Communication and Education </p><ul><li>Develop and deliver clear communication materials to educate employees about their benefits options. </li><li>Organize informational sessions, workshops, and open enrollment events. </li><li>Address employee inquiries and ensure a positive experience with benefits programs.</li></ul><ul><li>Collaborate with Law Department</li><li>Partner with HR service center</li></ul><p>Qualifications: </p><p>Education and Experience </p><ul><li>Bachelor’s degree in Human Resources, Business Administration, or a related field. </li><li>Minimum of 10 years of experience in employee benefits management with hands-on experience, including leading a team.</li><li>Certified Employee Benefits Specialist (CEBS) or similar credentials preferred. </li></ul><p>Skills and Competencies </p><ul><li>Strong knowledge of benefits laws and regulations. </li><li>Exceptional leadership and team management abilities. </li><li>Excellent communication, interpersonal, and problem-solving skills. </li><li>Proficiency in HRIS systems and benefits-related software. </li><li>Proficiency in Excel and Microsoft suite</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Feb 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Marketing, Neurology Customer Experience]]></title>
    <date><![CDATA[Mon, 02 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44931]]></requisitionid>
    <referencenumber><![CDATA[R44931]]></referencenumber>
    <apijobid><![CDATA[r44931]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44931/senior-director-marketing-neurology-customer-experience/]]></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 Director Marketing, Neurology Customer Experience, will contribute to the success of our emerging Neurology Business Unit and will report to the Executive Director, Marketing. This person will implement the approved Brand plan, and have primary responsibility to lead the development and implementation of the strategic and tactical plans/programs as it relates to our customer experience across the omnichannel environment for both HCP and consumer for our upcoming launch in Myasthenia Gravis.</p><p>This important role is responsible for leading the creation of an omnichannel strategy and execution across both HCP and consumer audiences. This includes the development and implementation of content strategy across customer groups: Physician / physician groups, Patients / caregivers. Develop deep insights through an understanding of customer preferences to shape our content strategy and direct team to implement across customers. Lead a team to deliver HCP and patient content with a passion for curated customized content across the customer journey.</p><p><strong>In this position a typical day may include the following:</strong></p><ul><li>For HCPs, the focus will be content production delivered through all digital channels for non-personal from home office initiatives as well as Next Best Action through Veeva CRM for field communication to their customers.</li><li>For patients the focus will be to activate the patients demonstrating the broad awareness while continuing to drive/maintain brand awareness. This includes advertising across all relevant media channels. Significantly increase our digital content offerings as well as enhancing our CRM program to include: lead generation and adherence.</li><li>Ensuring that marketing processes and programs align with corporate guidance, as well as regulatory, legal, and ethical guidelines.</li><li>Leading and providing development opportunities for direct reports.</li><li>This person will work closely with many cross functional teams including across the entire brand team, Market Access team, Insights and Analytics, Commercial IT</li><li>Monitoring spending against budget and managing projects to agreed-upon timelines, budgets, and scope.</li></ul><p><strong>This May Be the Right Role for You If you:</strong></p><ul><li>You have experience with a digital asset management system and Sales Force Cloud</li><li>You have expertise in behavioral science would be a plus.</li><li>You can demonstrate leadership qualities and have experience managing teams.</li><li>You are a strong communicator and can present well, capable of articulating complex strategies to partners of all levels, including Senior Leaders, regardless of their technical background.</li><li>You can complete and manage multiple projects in a fast-paced environment where quick decision making and clear direction is a must.</li><li>You bring organizational agility and the capability to reprioritize based on external or internal changes.</li><li>You can work effectively and efficiently with team members, across departments, and managing agencies.</li></ul><p>To be considered for this role,<strong> </strong>you must have a Bachelor's Degree, MBA preferred. The ideal candidate must have a minimum 15 years of progressive experience in biologics marketing and omnichannel strategy development and execution in the life sciences. Neurology experience is preferred and Myasthenia Gravis or Neurology Rare Disease experience a plus. Lastly, you will need to be onsite in Sleepy Hollow, NY 4 days a week.</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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Feb 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Epidemiology-Health Economics & Outcomes Research]]></title>
    <date><![CDATA[Mon, 02 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44671]]></requisitionid>
    <referencenumber><![CDATA[R44671]]></referencenumber>
    <apijobid><![CDATA[r44671]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44671/director-epidemiology-health-economics-outcomes-research/]]></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>As a Director, Epidemiology (HEOR) you will develop and drive real world evidence (RWE) that influences the development and commercialization of our innovative therapies. You will lead high impact epidemiologic research, apply innovative methods, and work with rich real world data sources answering complex questions for patients, clinicians, regulators, and payers.</p><p>This position is located at our Sleepy Hollow, NY offices and will require you to be on-site 4 days week. If eligible, we can offer relocation benefits. We cannot offer a fully remote option. </p><p><strong>A typical day may include the following: </strong><br>• Generate high quality observational research using RWD to support development and commercial strategies.<br>• Apply epidemiologic expertise to clinical development and trial design discussions, including opportunities for external control arms or hybrid evidence approaches.<br>• Support global HTA, payer, and regulatory submissions by generating epidemiology and RWE inputs for reimbursement packages and regulatory and value dossiers.<br>• Synthesize and critically evaluate scientific evidence to generate epidemiologic evidence for regulatory and payer submissions, press releases, and internal needs.<br>• Evaluate and implement emerging design and analytic methods enhancing our RWE capabilities.<br>• Stay current with evolving regulatory and payer expectations for RWE, guiding internal teams on implications for evidence strategy and generation.<br>• Represent the organization in external scientific, industry, and other forums, including peer reviewed publications and conference presentations to strengthen external visibility.</p><p><strong>This may be for you if you:</strong> <br>• You thrive in a team first environment and want to see your work inform decision making at scale.<br>• Have an innovation approach and enjoy developing solutions to complex problems<br>• Are at ease with an abundance of detail and complexity, yet mindful of the big picture.<br>• Can operate successfully in a ‘rapid response” environment<br>• Exceptional communication abilities that allow you to translate complex designs and findings into clear, actionable insights for a wide range of audiences.</p><p>To be considered it is required to have a PhD in Epidemiology or a related subject area supported by 7+ years of experience across academia, pharma/biotech, or consulting. Hands on leadership in developing study protocols and statistical analysis plans using real world data sources with a record of peer-reviewed publications is required. Expertise in advanced analytical methods for large healthcare datasets to apply or expand skills in machine learning. Familiarity with global HTA and payer evidence is advantageous.<br> </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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Feb 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director,  Program Operations Leader - Ophthalmology/Renal]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45092]]></requisitionid>
    <referencenumber><![CDATA[R45092]]></referencenumber>
    <apijobid><![CDATA[r45092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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. For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days 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><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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I- Dermatology- Los Angeles Central, CA]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44980]]></requisitionid>
    <referencenumber><![CDATA[R44980]]></referencenumber>
    <apijobid><![CDATA[r44980]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44980/medical-specialist-i-dermatology-los-angeles-central-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[<p><strong>Medical Specialist, Dermatology, Los Angeles Central, CA (MS)</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Allergy & Immunology]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44901]]></requisitionid>
    <referencenumber><![CDATA[R44901]]></referencenumber>
    <apijobid><![CDATA[r44901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44901/medical-director-clinical-development-allergy-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>The Medical Director, Clinical Sciences is responsible for facilitating assigned studies, providing investigator support of Regeneron driven studies, and may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into a Sr Medical Director, Clinical Sciences and is expected to have proficient knowledge of the drug development process, good clinical practice, study design and research methodology as well as understand Regulatory and compliance landscape in the pharmaceutical industry. This role utilizes scientific and clinical expertise to initiate, propose, design and execute research and development programs for early and/or late stage assets. 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. Some industry experience preferred.</p><p>A typical day in the life may include the following responsibilities:</p><ul><li>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program. Clinical deliverables may include individual protocols; clinical components of regulatory documents/registration dossier and brand related medical information, clinical communication and publications</li><li>Advanced analytical skills and ability to communicate concise and clear messages</li><li>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts</li><li>Ability to lead activities within a matrix environment</li><li>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally</li></ul><p>This role may be for you if:</p><ul><li>You are passionate about impacting entire populations of patients</li><li>You want to learn innovative approaches to drug development</li><li>You want to be a part of a collaborative, growing team</li></ul><p>In order to be considered for this role, a M.D. degree or equivalent is required. Specialized clinical fellowship training in Allergy, Immunology, Pulmonology, Dermatology or Infectious Diseases is strongly preferred. A minimum of 2-4 years of clinical development experience in industry is preferred, but academic research experience will be considered.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Manager - Dermatology　※Hokkaido, North Tohoku]]></title>
    <date><![CDATA[Sun, 15 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44772]]></requisitionid>
    <referencenumber><![CDATA[R44772]]></referencenumber>
    <apijobid><![CDATA[r44772]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44772/sales-manager-dermatology-hokkaido-north-tohoku/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Summary / Purpose of Position: </strong></p><p>The District Manager collaborates to build and sustain a high-performance team culture aligned with Regeneron's vision, values, and strategic direction. The manager oversees and leads a team of MRs (Medical Representatives) within the assigned region, effectively guiding and managing their performance to achieve sales targets. </p><p><strong>Assigned Area: </strong></p><p>You will be responsible for the Hokkaido, North Tohoku area.<br>Your residence will be in Sapporo.</p><p><strong>Responsibilities: </strong></p><p>Performance Orientation and Leadership: </p><p>- Recruit industry-leading sales representatives (MRs). </p><p>- Conduct training for new employees in collaboration with HR and talent development programs. </p><p>- Manage the performance of MRs in the assigned region by providing appropriate leadership and guidance. </p><p>- Provide targeted and effective feedback, coaching, training, development plans, and talent management for direct reports. </p><p>- Identify best practices and share them across the department. </p><p>- Build effective and productive partnerships with Regeneron's alliance companies. </p><p>- Enhance Regeneron's reputation and expand relationships with key HCPs (Healthcare Professionals). </p><p>Strategic Planning and Effective Execution: </p><p>- Ensure that direct reports acquire high-level knowledge of products, competitive treatments, and market environments to maximize opportunities for Dupilumab market expansion. </p><p>- Provide field input to relevant headquarters departments and assign clear tactical plans to team members, ensuring their execution. </p><p>- Monitor and track key performance indicators to achieve sales and behavioral goals in the assigned region, making adjustments as needed. </p><p>- Manage and allocate resources effectively to ensure sales targets and profitability are achieved. </p><p>- Manage budgets across the assigned region and demonstrate ROI for investments. </p><p>- Ensure agreed-upon advocacy development plans are achieved across the region. </p><p>- Provide performance summaries to relevant business functions (division and HR). </p><p>Regulatory and Corporate Compliance: </p><p>- Fully comply with industry and company procedures. </p><p>- Act in accordance with applicable pharmaceutical industry codes of conduct and Regeneron's SOPs (Standard Operating Procedures). </p><p><strong>Qualifications: </strong></p><p>- Degree or equivalent education in life sciences, pharmacy, chemistry, or biology preferred. </p><p>- Experience in first-line management (field team oversight). </p><p>- Engagement/experience with alliances. </p><p>- Talent management and leadership abilities. </p><p>- Proven track record in account management and sales performance in the pharmaceutical industry. </p><p>- Understanding of financial tools and processes required for brand plan execution. </p><p>- Demonstrated ability to identify opportunities and develop them into business solutions. </p><p>- Strong network, influence, and personal credibility. </p><p>- Ability to plan effectively and prioritize tasks. </p><p>- High-level communication and presentation skills. </p><p>- Excellent commercial insight. </p><p>- Proficiency in IT and digital tools, with the ability to handle data, multiple systems, and CRM. </p><p>- Certification in relevant pharmaceutical industry codes of conduct. </p><p>- Willingness to travel frequently as required by this role. </p><p>- Basic Excel and PowerPoint skills. </p><p><strong>Preferred Qualifications: </strong></p><p>- Knowledge of therapeutic areas (dermatology)and sales experience with biologics. </p><p>- Up-to-date clinical knowledge of therapeutic areas and competitive brands. </p><p>- Network with key opinion leaders in the dermatology field. </p><p>- English proficiency is desirable but not mandatory for this role. </p><p><strong>Minimum Education Requirements: </strong></p><p>- Bachelor’s degree from an accredited university in business, marketing, finance, economics, market research, statistics, social sciences, biological sciences, or physical sciences. </p><p>- At least 7 years of experience in the pharmaceutical industry or related professional experience. </p><p>- Valid driver’s license. </p><p>- MR certification.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Feb 2026 02:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Hematology)]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44824]]></requisitionid>
    <referencenumber><![CDATA[R44824]]></referencenumber>
    <apijobid><![CDATA[r44824]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44824/senior-manager-clinical-study-lead-hematology/]]></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>The <strong>Senior Clinical Study Lead</strong> (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is 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 out-sourced 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>This role is not eligible fully remote. This role is required to be onsite in one of our locations.</p><h3><strong>A typical day in this role looks like: </strong></h3><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Provides operational input into protocol development</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Ensures compliance with the clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors</p></li><li><p>Provides input into baseline budget development and management</p></li><li><p>Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level</p></li><li><p>Leads the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Oversees/conducts site evaluation and selection</p></li><li><p>Leads investigator meeting preparation and execution</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</p></li><li><p>Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Ensures accurate budget management and scope changes for internal and external studies</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Oversees the execution of the clinical study against planned timelines, deliverables and budget</p></li><li><p>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</p></li><li><p>Ensure clinical project audit and inspection readiness through the study lifecycle</p></li><li><p>Supports internal audit and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>Contributes to clinical study report writing and review</p></li><li><p>Facilitates and contributes to study level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables</p></li><li><p>Recommends and participates in cross-functional and departmental process improvement initiatives</p></li><li><p>Responsible for identification of innovative approaches to clinical study execution including global considerations 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><li><p>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require 25% travel</p></li></ul><h3><strong>This role may be for you if you have:</strong></h3><ul><li><p>Exceptional interpersonal & leadership skills</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Advanced communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Strong budget management experience</p></li><li><p>An awareness of relevant industry trends</p></li><li><p>Ability to build, lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Advanced project management skills, cross-functional team leadership and organizational skills</p></li><li><p>Line management experience</p></li></ul><p><strong>In order to be considered qualified, </strong>a minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience.</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Customer Insights - Neurology]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45023]]></requisitionid>
    <referencenumber><![CDATA[R45023]]></referencenumber>
    <apijobid><![CDATA[r45023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45023/director-customer-insights-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>Regeneron is seeking a Director, Insights & Analytics (I&A) to join our team! As part of an exciting upcoming launch in generalized myasthenia gravis (gMG), this role will play a critical role in shaping analytics, insights, and decision-making during a pivotal moment for the organization</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, I&A will report into an Executive Director, I&A within the Commercial Strategy and Insights and Analytics (CSI&A) department. This role will oversee a high-performing team (internal and external) responsible for generating actionable insights from a broad set of I&A sources, to inform business decisions. The role will partner with and serve as a strategic advisor to the Neurology Commercial Business Unit (CBU) and will partner with other leaders to grow and develop talent within the CSI&A team.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><p>1) Lead the I&A Neurology team in providing business analytics, customer insights and competitive intelligence to address all commercialization needs</p><p>2) Collaborate with the ED, I&A to set the strategic I&A direction that aligns with overarching priorities and helps drive launch excellence</p><p><em>Develop</em></p><p>3) Foster innovative solutions and a design-thinking approach aligned with strategies for the Neurology business.</p><p>4) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent</p><p>5) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform business decisions a rapidly developing Neurology CBU; and <strong>b)</strong> enhance brand differentiation and impact</p><p><em>Partnership and collaboration</em></p><p>6) Lead efforts to identify and crystalize insights that inform strategic plans</p><p>7) Collaborate with the Neurology CBU and other members of leadership to identify, predict and inform business decisions relating to the competitive outlook for gMG</p><p>8) 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>9) Coordinate alignment with stakeholders on all insights and analytics agendas</p><p>10) Work with other CSI&A leaders to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analysis, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>11) Proactively communicate with the Neurology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>12) Construct and deliver integrated business reviews, I&A summary overviews with leadership from Neurology and CSI&A</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum BS with 12+ (or MS with 10+) years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with market-leading brands required and neurology or rare disease experience is desired</p></li><li><p>Functional expertise in business analytics, HCP consumer/patient insights, primary research methods, analog forecast development and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, HCP consumer/patient 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></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[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Supplier Quality and Compliance]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43623]]></requisitionid>
    <referencenumber><![CDATA[R43623]]></referencenumber>
    <apijobid><![CDATA[r43623]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43623/associate-manager-supplier-quality-and-compliance/]]></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>The Associate Manager, Supplier Quality and Compliance will support the planning and execution of compliance initiatives utilizing the sourcing process for raw material manufacturers and distributers. The role supports and maintains all cGMP compliance aspects of Global Procurement operations under the direction and guidance of Sourcing Management. Ensures organization and timely completion of Approved Supplier List documentation in addition to Process deviations assigned to Sourcing (CAPAs, NOEs, EOEs) and supports closure of QA Audits related to audits of raw material manufacturers and distributers.</p><p><em><strong>This role requires onsite 5 days / week - this is not open to remote or hybrid work arrangements</strong></em></p><p><strong>In this role a typical day may include</strong></p><ul><li>Supports and proactively maintains all Sourcing cGMP procedures, documentation and training related to SOP and Work Instructions.</li><li>Supports and maintains Approved Supplier List (ASL).</li><li>Supports compliance needs and coordinates with other sites to ensure engagement, feedback and buy-in related to Global Procurement document revisions.</li><li>Supplier Audit Compliance: Drives successful audit closures by focusing on proactive issue resolutions and communication with suppliers to effect acceptable audit closures for raw materials.</li><li>Coordinates with Cross-Functional Compliance resources to support Global Procurement and Quality Auditing needs for acceptable closure of audit findings and to secure evidence that substantiates supplier commitments.</li><li>Tracks and reports CAPA to support audit closure.</li><li>Executes cGMP compliance documents and supports cGMP activities among the Global Procurement team.</li><li>Supports and assists with the management of Supplier Corrective Action Reports (SCARs)</li><li>Works closely with Legal, QA and Suppliers to help facilitate the execution and management of various agreements, as required.</li><li>Completes Global Procurement change controls to ensure they are done correctly and effectively.</li><li>Works with Global Procurement staff to review and drives timely closure of NOE / deviations and associated processes (CAPA).</li><li>Actions the Global Procurement responses to compliance related requests for data from Regulatory, Quality Assurance, Audit staff and other stakeholders.</li><li>Supports the Global Procurement staff as required for assigned categories and participates in other procurement office duties as assigned.</li></ul><p><br> </p><p><strong>This role may be for you if you have:</strong></p><ul><li>Excellent collaboration skills and the ability to work cross functionally across categories and internal stakeholders.</li><li>Understanding of cGMP systems and processes with a particular emphasis on compliance is strongly preferred.</li><li>Familiarity and experience working in an ERP system is preferred</li><li>Ability to build strong relationships with stakeholders and suppliers to drive results for Regeneron.</li><li>Demonstrated success supporting cross-functional teams to drive results in SCARs, ASLs, CAPAs, Change Notifications, and related Quality and Compliance processes.</li><li>Working & operating with integrity, focus, and clarity in an environment of ambiguity to drive change and improvement.</li><li>Continuous improvement mindset in identifying areas of improvements and working with leadership to implement them.</li></ul><p><strong>To be considered for this role you must possess</strong> a BS/BA in a related field and at least 6+ years of relevant experience in a cGMP environment, preferably in procurement, or equivalent combination of education and experience. Work experience within a biopharmaceutical company preferred. Microsoft Office required including strong PowerPoint and Excel skills.</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>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Baton Rouge, LA]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45099]]></requisitionid>
    <referencenumber><![CDATA[R45099]]></referencenumber>
    <apijobid><![CDATA[r45099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45099/medical-specialist-i-dermatology-baton-rouge-la/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Baton Rouge]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Baton Rouge, LA (Alexandria, Monroe)</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) – Dermatology Yamaguchi Area]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45400]]></requisitionid>
    <referencenumber><![CDATA[R45400]]></referencenumber>
    <apijobid><![CDATA[r45400]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45400/medical-representative-mr-dermatology-yamaguchi-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Assigned Area: </strong></p><p>You will primarily work in the Yamaguchi area. </p><p>Your residence is expected to be in Yamaguchi.(Fukuoka also available for consultation)</p><p><strong>Job Overview: </strong></p><p>While embodying Regeneron’s philosophy of "putting patients first," you will play a key role in the Immunology Department's dermatology division by managing Dupixent and achieving sales targets. </p><p>Utilizing excellent business acumen and strategic thinking, you will aim to achieve and exceed corporate goals by building trust-based relationships with customers and offering valuable solutions. </p><p><strong>Main Responsibilities: </strong></p><p>- Budget and expense management to achieve brand sales targets </p><p>- Developing and implementing annual business plans using market insights </p><p>- Building strategic sales plans based on key data </p><p>- Performing various administrative tasks (e.g., expense reporting, marketing reports) </p><p>- Compliance with regulations and legal requirements </p><p>- Participation in area meetings and nationwide conferences </p><p>- Completion of training programs and skill development </p><p>- Travel as needed (including nights and weekends) </p><p>- Conducting business safely while driving </p><p><strong>Required Skills and Experience: </strong></p><p>- Sales experience targeting university hospitals </p><p>- Specialized knowledge in dermatology and sales experience with biologics </p><p>- Excellent customer engagement and communication skills </p><p>- Strategic thinking and ability to work independently </p><p>- Proficiency in IT and digital tools </p><p>- Experience in joint promotions with alliance companies </p><p><strong>Preferred Qualifications: </strong></p><p>- Clinical knowledge of competitive brands or therapeutic areas </p><p>- Network with key opinion leaders in dermatology </p><p>- English proficiency is a plus </p><p><strong>Eligibility: </strong></p><p>- Bachelor’s degree (or equivalent qualification) </p><p>- Over 5 years of sales experience in the pharmaceutical industry </p><p>- MR certification and a valid driver’s license </p><p><strong>Advance Your Career to the Next Level: </strong></p><p>Regeneron provides an environment where every employee can maximize their potential. This is a rewarding position that allows you to leverage your expertise in the dermatology field to deliver significant value to patients and healthcare professionals. This challenge offers an opportunity to elevate your career to new heights.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 02:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sample Management Associate]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44409]]></requisitionid>
    <referencenumber><![CDATA[R44409]]></referencenumber>
    <apijobid><![CDATA[r44409]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44409/sample-management-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>A Sample Management Associate supports biobanking operations efficiently and effectively while beginning to independently manage sample data processes. Possesses a thorough knowledge and understanding of clinical/non-clinical study protocols and associated documentation. Is fully capable of multi-tasking across assignments. Works with clients directly in a team environment. The incumbent may help in assessing and investigating new opportunities that will lead to increased efficiencies and improved productivity with regards to biobanking operations.</p><h3>As a Sample Management Associate, a typical day may include:</h3><ul><li><p>Trains on clinical/non-clinical study protocols and associated study documentation to build knowledge of study conduct as it pertains to biospecimen management. Executes study reference file creation by interpreting protocols and other applicable data inputs with guidance.</p></li><li><p>Performs the accessioning and receipt of non-clinical/clinical samples by assessing and verifying data, both manually and with automated platforms such as Microsoft VBA and Streamlit. May identify and communicate issues with automated platforms to drive resolution.</p></li><li><p>Has an in-depth knowledge of Microsoft Excel and can analyze discrepancies in sample metadata using complex formulas with limited guidance.</p></li><li><p>Executes necessary operations in applicable software systems (e.g., LIMS, ELN, etc.) to perform specimen and data management. Has the ability to identify and troubleshoot routine challenges.</p></li><li><p>Fulfills clinical/non-clinical sample requests to support bioanalysis deliverables as well as company-wide research initiatives.</p></li><li><p>Facilitates the completion and review sample transfer documentation, as applicable.</p></li><li><p>Responsible for assigning and coordinating sample management activities for assigned programs under limited guidance.</p></li><li><p>Under supervision, executes the reconciliation and data cleaning of biospecimens to drive deliverables forward.</p></li><li><p>May be responsible for the review of study documents to support study start up and protocol amendments.</p></li></ul><h3>This role may be for you if you:</h3><ul><li><p>Collaborates and maintains effective verbal and written communication with internal and/or external stakeholders to facilitate data discrepancy resolution. Communicates with CRO’s and third-party vendors to support biospecimen operations.</p></li><li><p>Is capable of identifying and troubleshooting problems pertaining to clinical/non-clinical protocols and associated documents as well as routine sample management processes and/or procedures.</p></li><li><p>Ensures a state of audit readiness. Assists in the preparation of supporting documents for Quality Audits, as applicable. May participate in study audit activities.</p></li><li><p>Handles high priority and high volume tasks within the appropriate timeframe while maintaining accuracy. Adapts to changing priorities. Is capable of multi-tasking across assignments.</p></li><li><p>Provides cross-functional support to other sample management teams, as needed.</p></li><li><p>May assist with the training of other laboratory staff.</p></li><li><p>Participates in sub-group meetings and may shares results or progress of work with others.</p></li><li><p>Ensures compliance and proper documentation in accordance with SOPs, and applicable regulations.</p></li><li><p>Communicates effectively with his/her manager and actively seeks out feedback to deepen self-development.</p></li><li><p>Responsible for his/her own safety in the laboratory, as well as for the safety of co-workers and visitors.</p></li></ul><h3>To be considered, you must have:</h3><p>Minimum of a Bachelors Degree + 2+ years experience</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>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Lab Assistant, PMPD]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45250]]></requisitionid>
    <referencenumber><![CDATA[R45250]]></referencenumber>
    <apijobid><![CDATA[r45250]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45250/senior-lab-assistant-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[<div><p>We are seeking a Senior Lab Assistant to join the Laboratory Operations (LabOps) team within the Product, Analytical, and Process Development (PAPD) Operations group, which primarily supports the Pre-Clinical Manufacturing and Process Development (PMPD) department. </p></div><div><p>The LabOps team executes routine laboratory operations essential to PMPD’s core mission, including daily restocking and ordering of consumables, preparing media and buffers for use by lab personnel, and washing and sterilizing bottles and bioreactors. We are seeking someone to lead media and buffer preparation activities, including receiving customer requests, organizing schedules, distributing work across LabOps personnel, and ensuring adequate raw material inventory from both external vendors and our manufacturing organization. </p></div><div><p> <br><strong>A Typical Day in the Role Might Look Like:</strong> </p></div><div><ul><li><p>Prepare buffers/media for various formulations, including pumping into single-use bags and recording appropriately into an electronic lab notebook </p></li></ul></div><div><ul><li><p>Maintain clean, organized lab, storage, and hallway spaces to support a safe working environment. </p></li></ul></div><div><ul><li><p>Manage the customer request portal, prioritize and delegate tasks to LabOps personnel to meet need-by dates while delivering high-quality customer service, and develop a strong understanding of customer needs and workflows. </p></li></ul></div><div><ul><li><p>Oversee raw material ordering by placing orders with external vendors and collaborating with colleagues to initiate move orders for critical items stored in manufacturing facilities. </p></li></ul></div><div><ul><li><p>Provide hands-on in-lab support and serve as a team lead and/or project coordinator to ensure appropriate training, efficient workflows, and reliable delivery on commitments. </p></li></ul></div><div><ul><li><p>Anticipate and recognize potential issues, communicate them to the supervisor, and identify operational improvements while implementing strategies that increase speed and efficiency. </p></li></ul></div><div><ul><li><p>Communicate effectively across functions and levels and demonstrate strong interpersonal and customer-service skills, leveraging prior technical experience and knowledge. </p></li></ul></div><div><ul><li><p>Adapt to evolving priorities and processes to continuously support the department through future growth and expansion </p></li></ul></div><div></div><div><p><strong>This Role Might Be For You If You:</strong> </p></div><div><ul><li><p>Possess good organization, communication, and collaboration skills, and can thrive both independently and within a team </p></li></ul></div><div><ul><li><p>Have a service-oriented mindset and a passion for delivering quality customer service. </p></li></ul></div><div><ul><li><p>Demonstrate interest in science and strong attention to detail </p></li></ul></div><div><ul><li><p>Are comfortable asking questions, receiving feedback, and continuously improving your skills and knowledge. </p></li></ul></div><div><ul><li><p>Drive efficient progress and execute core responsibilities independently with limited supervisory guidance. </p></li></ul></div><div><p>This role requires a HS diploma, and 2 - 4+ years’ experience, or combination of training and experience. Experience in media/buffer prep or science background a plus </p></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 (hourly)</strong></strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Boston Central, MA]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45726]]></requisitionid>
    <referencenumber><![CDATA[R45726]]></referencenumber>
    <apijobid><![CDATA[r45726]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45726/medical-specialist-i-dermatology-boston-central-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[<p><strong>Geography: Boston Central, MA</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Systems Engineer]]></title>
    <date><![CDATA[Tue, 24 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44201]]></requisitionid>
    <referencenumber><![CDATA[R44201]]></referencenumber>
    <apijobid><![CDATA[r44201]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44201/principal-it-systems-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[<p>We are seeking a highly skilled and proactive Principal IT Systems Engineer to join our dynamic team, reporting directly to the Services Delivery Manager for Performance, Alerting, & Observability. The role will play a critical role in maintaining the reliability, uptime, availability, and performance of our IOPS IT server and infrastructure environments, as well as managing compliance solutions. This position is instrumental in ensuring the stability and operational efficiency of our IT infrastructure while strictly adhering to Good Manufacturing Practice (GMP) standards.</p><p>As a Principal IT Systems Engineer, a typical day might include the following:</p><ul><li>Proactively monitor and maintain Windows Server environments to guarantee efficient performance and reliability.</li><li>Configure and manage virtualized environments, including virtual machines, storage, and networking, to meet evolving business needs.</li><li>Identify and resolve issues in a timely manner, ensuring high availability, security, and resilience of network resources.</li><li>Conduct detailed root cause analysis and implement corrective actions to prevent recurrence, improving system reliability.</li><li>Develop and maintain comprehensive documentation of processes, procedures, and best practices to facilitate knowledge sharing and training.</li><li>Ensure rigorous compliance with GMP standards across all relevant processes and systems.</li><li>Implement and manage robust change control processes to uphold system integrity and compliance.</li><li>Collaborate with security teams to ensure IAM systems and infrastructure align with organizational security policies and frameworks.</li></ul><p>This Role May Be for You If You Have:</p><ul><li>A unique blend of IT operations expertise and system engineering, with a robust background in Windows Servers, Virtualization, Cloud platforms (AWS & Oracle), and Security Operations</li><li>Demonstrated experience with:<ul><li>SailPoint for identity governance and lifecycle management.</li><li>CyberArk for privileged access management.</li><li>Ivanti for exposure management.</li><li>Nexthink for visibility and control over employee experience</li><li>Axonious for overall environment visibility.</li><li>High Performance Computing (HPC) for complex problem solving.</li><li>Familiarity with PowerShell, Python, or Bash scripting.</li><li>Virtualization technologies and cloud platforms, including virtual machine management and configuration.</li></ul></li></ul><p>In order to be considered for this position, you must hold a BA/BS degree in Computer Science or related field and</p><ul><li>Principal IT Systems Engineer: 8+ years of relevant experience with data center technologies (VMware, NetApp, Dell EMC storage), backup solutions, and IT and Security operations.</li><li>Staff IT Systems Engineer: 10+ ears of relevant experience with data center technologies (VMware, NetApp, Dell EMC storage), backup solutions, and IT and Security operations.</li><li>3-5 years of experience in system administration, network engineering, or a related role desired. Experience working in GMP environments and ensuring compliance with relevant standards preferred.</li><li>Relevant certifications (e.g., MCSE, VCP, CCNA, SailPoint, CyberArk) are a plus.</li><li>Preferred knowledge of understanding of IT compliance guidelines, including PICS, CFR21 Part 11, Annex 11, and GAMP.</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>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Feb 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Respiratory (NYC)]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45745]]></requisitionid>
    <referencenumber><![CDATA[R45745]]></referencenumber>
    <apijobid><![CDATA[r45745]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45745/associate-director-field-medical-affairs-respiratory-nyc/]]></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>As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within Respiratory to support the clinical and business objectives across the product life cycle. We deliver strategic and operational support by establishing, developing and maintaining scientific exchange with medical specialists, health care professionals, and payers, aligned with our strategic objectives. We provide clinical and health economic information that enhances the value and appropriate use of Regeneron products. You will work with clinical research sites and investigators, and support of research activities as directed by the Global Medical Functional head.</p><p>Responsibilities of this role are to ensure accurate exchange and distribution of clinical and scientific information relevant to in-line and pipeline products in a timely, ethical and customer-focused manner.</p><p><strong>Territory:</strong> New York City</p><p><strong>A typical day may include</strong></p><p>•Engage in scientific discussions with medical and scientific specialists, including Healthcare Professionals and population health decision makers (“payers”) consistent with Medical Affairs objectives.</p><p>•Demonstrate deep scientific expertise related to assigned molecules/products and the associated therapeutic area to exchange relevant information and insights with specialists within a region.</p><p>•Build and develop relationships with key external scientific and medical specialists and organizations in a region to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape.</p><p>•Shape and execute local medical strategy based on Global Medical Affairs strategy within planned timelines.</p><p><strong>This may be for you if:</strong></p><p>•Enjoy working independently in the field, while having an impact on the company’s mission.</p><p>•You are passionate about developing knowledge of and sharing clinical scientific data.</p><p>•You like working collaboratively and developing relationships in academic and clinical practice settings.</p><p>•You have the innate ability to balance multiple initiatives, prioritize them and execute them independently, while excelling at keeping all partners advised and engaged.</p><p>To be considered for this position, you must have an advanced Clinical/Science Degree (e.g., MD, PharmD, PhD) with a minimum of 5 years related work experience (clinical, managed care, or industry experience). Experience as an MSL or in a Field Medical Affairs representative with Immunology is required. Respiratory experience is preferred, It is required to have the ability to communicate and disseminate scientific and clinical data. Residency in the territory is required.</p><p>#msl #medicalscienceliaison</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Data Management]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45811]]></requisitionid>
    <referencenumber><![CDATA[R45811]]></referencenumber>
    <apijobid><![CDATA[r45811]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45811/process-development-engineer-iii-data-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>Role Summary</strong></p><p>The Data Enablement and Analytics (DEA) team within PAPD drives digitalization by making data usable, reliable, and impactful across process development. We are seeking a Data Solutions Engineer with deep expertise in LIMS solutions like <strong>LabWare LIMS or Benchling</strong> and enable analytics from this data. This person will serve as a functional and technical bridge between laboratory users, process development scientists, and digital/data platforms.</p><p>This role is critical to ensuring high‑quality data capture, governance, integration, and reporting across PAPD workflows. The ideal candidate combines strong LIMS domain knowledge with hands‑on experience in data platforms (data lakes and data stores) and reporting/visualization tools and brings excellent communication and collaboration skills.<br> </p><p><strong>Key Responsibilities</strong></p><p><strong>LIMS Platform Ownership & Support</strong></p><ul><li>Act as a <strong>superuser and subject‑matter expert</strong> for <strong>LabWare and Benchling Lab information management systems (LIMS)</strong>, supporting day‑to‑day PAPD laboratory operations.</li><li>Work with IT and our LIMS vendors to support onboarding, training, and adoption of new LIMS capabilities across PAPD.</li><li>Partner with laboratory scientists, process engineers, and data teams to optimize LIMS configurations, workflows, templates, and metadata standards.</li><li>Troubleshoot LIMS issues, coordinate with vendors/IT, and drive continuous improvement.</li></ul><p><br><strong>Reporting & Analytics Enablement</strong></p><ul><li>Enable and support reporting and visualization using <strong>Spotfire, Tableau, and Power BI</strong>, ensuring PAPD data from various data sources is usable for operational, scientific, and management insights.</li><li>Work with stakeholders to define key metrics, dashboards, and reporting requirements tied to PAPD processes.</li></ul><p><br><strong>Data Integration & Digital Enablement</strong></p><ul><li>Ensure LIMS data is <strong>complete, consistent, and analysis‑ready</strong>, supporting downstream consumption by data lakes, data stores, and analytics platforms.</li><li>Collaborate with DEA data engineering and OT/IT partners to enable reliable data pipelines from LIMS into enterprise data platforms.</li><li>Contribute to creation of data standards, data quality checks, and documentation that support scalable digital solutions.</li></ul><p><br><strong>PAPD Process & Documentation</strong></p><ul><li>Apply strong knowledge of <strong>PAPD processes, workflows, and documentation practices</strong> to ensure digital solutions align with how work is performed in the labs.</li><li>Support documentation, data traceability, and audit readiness as required.</li></ul><p><br><strong>Collaboration & Agile Execution</strong></p><ul><li>Serve as a <strong>team player and connector</strong> across PAPD, DEA, IT, and external vendors and execute using <strong>SAFe </strong>(Scaled Agile Frameworks).</li><li>Translate between scientific, technical, and business stakeholders with clear, concise communication.</li><li>Act as the overall product owner and product manager for multiple agile teams and drive forward the PAPD roadmap using Agile methodology.</li><li>Participate in cross‑functional initiatives supporting PAPD’s broader digital and data strategy.</li></ul><p><br><strong>Required Qualifications</strong></p><ul><li>Bachelor’s degree in science, Engineering, Information Systems, or a related field (or equivalent experience) with 8+ years of total experience.</li></ul><ul><li>Good understanding of <strong>LIMS Solutions</strong> and hands‑on experience with <strong>LabWare </strong>or<strong> Benchling </strong>LIMS solutions.</li></ul><ul><li>Strong understanding of <strong>laboratory data flows</strong>, sample management, and experimental workflows.</li><li>Working knowledge of <strong>data lakes, data stores, and data integration concepts</strong>.</li><li>Experience enabling reporting or analytics using <strong>Spotfire, Tableau, and/or Power BI</strong>.</li><li>Solid understanding of <strong>PAPD process development environments and documentation</strong>.</li><li>Strong communication skills and ability to work effectively in cross‑functional teams.</li></ul><p><br><strong>Preferred Qualifications</strong></p><ul><li>Experience working within biopharma or biotech process development organizations.</li><li>Familiarity with upstream and downstream processing and analytics needs in a biopharma company.</li><li>Familiarity with data governance, metadata standards, and data quality practices.</li><li>Experience partnering with IT, data engineering, or digital transformation teams.</li><li>Familiarity with AI capabilities of Tableau Cloud, Power BI tools or similar.</li></ul><p><br><strong>Why Join DEA & PAPD</strong></p><ul><li>Play a key role in PAPD’s digital transformation and data strategy.</li><li>Work at the intersection of laboratory science, data platforms, and analytics.</li><li>Collaborate with a highly cross‑functional team supporting Regeneron’s mission to bring new medicines to patients.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Change Communications]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45838]]></requisitionid>
    <referencenumber><![CDATA[R45838]]></referencenumber>
    <apijobid><![CDATA[r45838]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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><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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Microbiology Scientist]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45750]]></requisitionid>
    <referencenumber><![CDATA[R45750]]></referencenumber>
    <apijobid><![CDATA[r45750]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45750/sr-microbiology-scientist/]]></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>Regeneron is currently looking for a QC (Quality Control) Microbiology Scientist to join our QC Technical Resources team. This position will specialize in microbiology test methods; provide critical microbiology support to cell-culture, manufacturing (drug substance and drug product), and facilities. They will ensure departmental compliance to regulatory guidelines are maintained and drive continuous improvements for microbiological methods.</div><div><p>A typical day as a QC Microbiology Scientist might include:</p><ul><li>Ensure QC microbiological compliance with cGMP standards. </li><li>Conduct microbiological validations for raw materials, finished products, in-process controls, and buffers.</li><li>Participate in cleaning and process validation activities involving microbiology.</li><li>Investigate and review alert and action limits, microbiological product OOS results and DNFs, implementing corrective actions as needed. </li><li>Develop, validate, and troubleshoot microbiological test methods, including rapid and alternative technologies.</li><li>Lead data gathering, analysis and reporting to support investigations and streamline processes.</li><li>Lead and participate in validations, studies, and investigations at CMO/CLOs and apply advanced scientific expertise to resolve complex issues.</li><li>Create, revise, and review microbiological documentation.</li><li>Assist manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice as needed.</li><li>Support the maintenance of reference libraries for microbiological methods.</li><li>Participate in internal audits, technical discussions and problem-solving with external entities.</li><li>Assist in the integration of technical updates into team procedures while maintaining regulatory compliance.</li><li>Provide technical advice to manufacturing personnel and effectively communicate solutions with the organization.</li><li>Drive continuous improvement of microbiological methods by staying current with industry trends, implementing updates into QC practices, and onboarding alternative and rapid technologies while serving as the SME for these innovations. </li><li>Contribute to the preparation and revision of technical proposals, amendments, reports, memoranda, and microbiological SOP.</li><li>Represent microbiology in cross-functional site meetings and provide technical advice to manufacturing personnel.</li><li>Participate in the transfer of methodologies to and from other test facilities. </li><li>Assist in the preparation for internal, customer, and regulatory inspections.</li><li>Proactively identify and implement laboratory process improvements and lean initiatives. Drive the integration of alternative and rapid technologies into QC practices.</li></ul><h3>This role might be for you if you:</h3><ul><li>Facilitate with organizational agility.</li><li>Assist in the development and support of strategies on how to achieve what needs to be done and develops metrics to measure the strategy.</li><li>Have knowledge of Microbiological Test Methods (Endotoxin, Low Endotoxin Recovery, Bioburden, Sterility etc.) associated with Drug Substance, Drug Product; Gene Therapy, Raw Materials, Utilities and Disinfectants</li><li>Possesses excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company.</li><li>Resolves and negotiates conflicts or problems with tact, diplomacy and composure.</li><li>Able to prioritize multiple priorities with outstanding organizational and time management skills.</li><li>Proficient in IOPS Systems (e.g. BMRAM, Discoverant, Documentation Compliance, LIMS, Microsoft Word, Microsoft Excel, Process Compliance).</li></ul><p>To be considered for the QC Microbiology Scientist you must have a BS/BA in Life sciences, microbiology or biology is preferred, and 5+ years of relevant experience. Previous experience working in a microbiology lab or pharmaceutical microbiology lab is preferred.</p></div><p>Level will be determined based on experience.</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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 12:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Data Architect - AI]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44113]]></requisitionid>
    <referencenumber><![CDATA[R44113]]></referencenumber>
    <apijobid><![CDATA[r44113]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44113/staff-data-architect-ai/]]></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>The Staff Data Architect - AI supports the design and implementation of modern data architecture with a focus on enabling AI and machine learning capabilities across our bio-manufacturing operations.</p><p>As a Staff Data Architect - AI, a typical day might include the following:</p><ul><li>Develop solutions by studying data needs, analyzing user requirements, and following Regeneron software development lifecycle.</li><li>Create design and documentation of data architecture standards with a focus on building infrastructure ready for AI/ML workloads.</li><li>Examine processes and systems to optimize, consolidate and analyze diverse data sets including structured, semi-structured and unstructured.</li><li>Create the technical documentation of solutions utilizing standards, templates, and procedures.</li><li>Design scalable data pipelines that feed predictive and generative AI models, as well as process monitoring tools.</li><li>Lead the development and maintenance of enterprise data models and reference architectures, with an emphasis on clean, well-structured data that AI systems can reliably consume.</li><li>Implement of cloud-native data infrastructure (AWS, Azure) including data lakes, feature stores, and model serving layers.</li><li>Collaborate with data and system owners, data scientists, and AI users to understand data requirements and ensure the architecture supports both current and future AI use cases.</li><li>Participate in architecture reviews, documenting design decisions and flagging potential risks or gaps.</li><li>Learn and apply governance and data integrity standards in a GxP environment.</li><li>Assist in the technical documentation of solutions utilizing standards, templates, and procedures. Independently manage small project related assignments ensuring on time delivery.</li></ul><p>This role may be for you if you have:</p><ul><li>Knowledge of data modeling, database design, and data pipeline development</li><li>Hands-on experience or strong academic/project exposure to architecture design and implementation of data pipelines in Azure and AWS. Experience with Databricks is a plus.</li><li>Experience with AI/ML data concepts such as feature engineering, data versioning, model training pipelines, or vector databases is a strong plus.</li><li>Understanding of integration patterns and APIs for connecting disparate data sources</li><li>Curiosity about how modern data approaches — data mesh, data fabric, lake house architectures — can support AI at scale.</li><li>Strong communication skills and a willingness to collaborate across technical and operational teams.</li><li>Experience with Version Control Software (SVN, Git, etc.).</li><li>Quality focused with strong attention to detail.</li></ul><p>In order to be considered for this position, you must hold a BA/BS in Computer Science, Bioinformatics, or related field and</p><ul><li>Staff: 10+ years relevant experience</li><li>Senior Staff: 12+ years of relevant experience</li><li>Experience in biotech, pharmaceutical, or other life sciences industries preferred</li><li>Cloud platform experience (AWS, Azure), workflow orchestration tools (Airflow, Luigi, Prefect, or similar), containerization technologies and scientific data management systems and experience with using GenAI to enhance own work</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>$108,000.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Manager Automation]]></title>
    <date><![CDATA[Fri, 06 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45447]]></requisitionid>
    <referencenumber><![CDATA[R45447]]></referencenumber>
    <apijobid><![CDATA[r45447]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45447/sr-manager-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Sr/Automation Manager who will be responsible for leading the design, implementation, validation, and lifecycle management of automation systems supporting bioprocessing, laboratory, and manufacturing operations. This role will ensure operational efficiency, regulatory compliance, data integrity, and continuous improvement across all automated platforms within a regulated biotech environment.</p><p><strong>As a Sr/Manager Automation, a typical day might include the following: </strong></p><ul><li>Managing a team of FTE’s and contractors in order to meet end user requirements</li><li>Working with System Owners to prioritize change control requests, releases and enhancements</li><li>Providing oversight for the design, implementation, and support of automation equipment</li><li>Maintaining adherence to ALCOA+ data integrity principles</li><li>Developing, implementing and driving operational rigor and discipline using metrics and other operational controls as needed</li><li>Presenting status of System Operations and Project Status to executive stakeholders and ensuring alignment of resources to key priorities</li><li>Developing continuous improvement ideas that improve team performance and efficiencies</li><li>Ensuring projects are completed on time and within budget</li></ul><ul><li>Performing monthly staff performance reviews and developing annual performance evaluation of staff</li><li>Developing and executing the site automation strategy aligned with business and operational goals</li><li>Capable of leading cross-functional automation projects from concept through commissioning and validation</li><li>Overseeing automation budgets, project timelines, and external vendor partnerships</li><li>Ensuring compliance with 21 CFR Part 11 and GxP requirements</li><li>Supporting internal and external regulatory audits</li><li>Ensuring automation systems comply with regulatory agencies, IOPS policies and procedures requirements</li><li>Supporting digital transformation and Industry 4.0 initiatives</li><li>Coordinating preventative and corrective maintenance programs</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>You are a self-starter with high initiative and possess a data-driven approach to problem-solving</li><li>You demonstrate strong interpersonal skills and have previous experience managing a team</li><li>You are experienced operating with integrity, focus, and clarity in an environment of ambiguity to drive change and improvement</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better</li><li>Can balance changing priorities with increasing workload by making/communicating timely decisions</li></ul><p>To be considered for this position you should have a BSc/BA in IT/Automation/Analytics or related field and the following minimum years of relevant industry experience for each level:</p><p>Manager: 7+ years</p><p>Senior Manager: 8+ years</p><p>#REGNIRLTO #LI-Onsite #JOBSIEST #IRELIM </p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 05:26:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Portfolio & Resource Management]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45484]]></requisitionid>
    <referencenumber><![CDATA[R45484]]></referencenumber>
    <apijobid><![CDATA[r45484]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45484/executive-director-portfolio-resource-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>The <strong>Executive Director, Portfolio Management</strong> is a key member of the Program and Portfolio Management (PPM) Leadership Team. This function plays an important role in optimizing the portfolio of programs in Regeneron’s product pipeline. The Executive Director will lead a group that integrates the entire development portfolio makeup and cross functional resourcing of post-research assets through lifecycle management to enable efficient portfolio decision making by executive leadership. The role will interface with senior management across Research, Development, Manufacturing and Commercial to ensure Portfolio Management excellence to drive pipeline delivery & portfolio value. This role will partner with Clinical Development Unit Heads, Functional Leaders, Global Program Heads and Program Management to deliver portfolio level information and analysis across the integrated development plans for all assets in development. The candidate will also be responsible for influencing asset and portfolio level decisions through identification of interdependencies and downstream implications of drug development decisions. </p><p><strong>Key Responsibilities</strong></p><ul><li>Provide leadership and strategic vision for the Portfolio Management group, supporting Clinical Development Units, cross-functional Strategic Program Teams (SPT’s) for all clinical assets.</li><li>Partners with Global Program Heads (GPH’s) and key functional leaders to ensure data enabled, timely portfolio and asset level decision making with key inputs from Research, Development, Manufacturing and Commercial. </li><li>Identify and champion Portfolio and Asset Development best practices, including the use of dashboards, templates, tools, systems and processes to drive efficiency, alignment, decision making, and communication - all leading to effective product planning and delivery.</li><li>Leverage Program and organizational knowledge, leadership, and facilitation skills to enable Program and Portfolio Management Teams to drive alignment, collaboration, and accountability within the SPTs and across corporate functions resulting in achievement of company and program goals.</li><li>Drive portfolio level program planning, including cross-functional resource planning, financial, and capacity assessments; contribute to long-range and budgetary planning.</li><li>Ensure effective communication of Program and Portfolio Management information to the broader organization.</li><li>Lead program and portfolio communication and reporting in partnership with executives and functional leaders, including developing and delivering monthly dashboards and program and portfolio reviews to the Executive Team, key business partners, and the Board of Directors. This covers pipeline content, portfolio metrics, development and portfolio reporting across all Therapeutic Areas (TA’s).</li><li>Develop strong working relationships with key stakeholders within and outside of Regeneron (functional leaders, peers, vendors, pharma industry community, and external opinion leaders).</li><li>Provide information to support portfolio decision making aligned with decisions on progression of individual assets.</li></ul><p><strong>Candidate Requirements</strong></p><ul><li>17+ years of pharmaceutical/biotech industry experience and a minimum of six years in program, portfolio and/or alliance management.</li><li>BA/BS in business, finance, science/technology, or related field required, advanced degree strongly preferred but not required. MS/PhD or MBA with experience working within a science-based life sciences organization.</li><li>Extensive knowledge of research and development and thorough understanding of the tasks required in all stages of drug development.</li><li>A strong understanding of the people, processes and infrastructure involved in managing across the drug development lifecycle.</li><li>Comprehensive knowledge of Program, Portfolio and Resource Management methodologies and techniques.</li><li>Ability to prioritize multiple tasks and options with a strong attention to detail.</li><li>Excellent written and verbal communication skills; strong communicator and influencer within all levels of the organization, including executive leadership. Knows what information and discussions are needed to help drive decisions and solve issues.</li><li>Strong analytical capabilities, including quantitative and qualitative assessment skills and demonstrated critical thinking skills.</li><li>Ability to distill complex issues and ideas down to simple comprehensible terms and issue resolution.</li><li>Exceptional ability to lead people and multidisciplinary functional groups, identify and develop talent, and delegate effectively.</li><li>Strong conflict resolution and problem-solving skills.</li><li>Strong leadership and team building skills.</li><li>Demonstrated capability to drive transformational change at the divisional and Enterprise scale.</li></ul><br><h3><strong>The ideal candidate will demonstrate the following competencies:</strong></h3><ul><li>Ability to work effectively in a fast-paced, rapidly changing and expanding environment and to juggle multiple large-scale projects, programs and enterprise- wide initiatives in a global organization.</li><li>Outstanding work ethic and integrity, including high ethical and quality standards.</li><li>Strong interpersonal skills particularly motivational, negotiation, listening, judgment, analytic, and conflict management skills, demonstrated by ability to lead teams.</li><li>Ability to engage in collaborative decision making, complete tasks in a timely fashion, and function in a rapid-paced environment. Must be a practical thinker, able to identify simple, realizable solutions.</li><li>Makes the best decision possible based on a mixture of data analysis, wisdom, experience, and judgement.</li><li>Creates a climate in which people want to do their best and can motivate many kinds of direct reports and team or Program members.</li><li>Can deal comfortably with executive leadership.</li><li>Knows how to get things done both through formal channels and the informal network and can inspire and motivate teams across the organization.</li><li>Possesses the courage to say what needs to be said and the interpersonal savvy to maintain credibility and relationships after saying it.</li><li>Comfortable with various personal styles; able to elicit contributions from introverts and to participate in passionate debates without taking the arguments personally or personalizing the arguments.</li><li>Works to reduce bureaucracy, able to distinguish necessary process from excessive complexity.</li><li>Impact-driven, not status or role-driven.</li><li>Proven ability to develop and lead a successful business plan, along with the flexibility and humility to “roll up your sleeves” to execute with excellence.</li><li>Comfortable with ambiguity and occasional chaos; cool under fire.</li><li>For best fit, the candidate must have the ability and strong desire to “make things happen”; and must have a results-oriented work ethic, a positive can-do attitude and be a bold, critical, and collaborative thinker.</li><li>Advanced knowledge of MS Project, Planisware, Planview and/or other project and portfolio planning and tracking software programs is required.</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Clinical Data Management]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42183]]></requisitionid>
    <referencenumber><![CDATA[R42183]]></referencenumber>
    <apijobid><![CDATA[r42183]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42183/associate-director-external-clinical-data-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>The Associate Director, External Data Services, plays a critical leadership role, overseeing team members to ensure all activities align with Regeneron’s procedures and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver structured external data in compliance with Regeneron SOPs. The role also involves coaching, mentoring, and managing the performance of direct reports, while contributing to the department's strategic direction. Additionally, the AD works with senior leadership to define goals, staffing needs, and departmental structure.</p><p><strong>A typical day in the life as an Associate Director, External Data Services includes: </strong></p><ul><li><p>Shape and implement the strategy for External Data Services.</p></li><li><p>Lead and manage a team of External Data Services Managers and Specialists.</p></li><li><p>Oversee the development and maintenance of all DTS documents, ensuring alignment with Regeneron standards, processes, and timelines.</p></li><li><p>Drive the External Data Vendor Oversight model, establishing effective communication, partnership-level processes, and portfolio-level transparency on DTS status and escalations.</p></li><li><p>Represent External Data Services in leadership forums and technology discussions.</p></li><li><p>Contribute to and execute the External Data Services technology strategy.</p></li><li><p>Provide expert-level guidance to CROs, stakeholders, and external vendors on External Data Services.</p></li><li><p>Identify process gaps and lead initiatives to improve processes.</p></li><li><p>Track milestones and deliverables, escalate issues, and communicate portfolio-level updates to stakeholders.</p></li><li><p>Lead or contribute to special projects requiring strategic input and expertise in External Data.</p></li><li><p>Serve as a subject matter expert (SME) for complex topics requiring leadership-level commitment.</p></li><li><p>Develop SOPs, Work Instructions, Guidance Manuals, and other DTS development tools.</p></li><li><p>Provide coaching, mentoring, and performance management for direct reports.</p></li><li><p>Manage resource allocation and planning for External Data Services.</p></li></ul><p><strong>This Role Might Be for You If You:</strong></p><ul><li><p>Have expert knowledge of regulations like 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards for data collection.</p></li><li><p>Possess deep expertise in Data Management, External Data processes, and industry best practices.</p></li><li><p>Demonstrate advanced experience with extracting data in SAS, CSV, and XML formats.</p></li><li><p>Can address complex External Data challenges and recommend actionable solutions.</p></li><li><p>Have a proven ability to develop best practices and processes to achieve objectives.</p></li><li><p>Exhibit strong problem-solving, analytical, and project management skills.</p></li><li><p>Thrive in a matrix environment with virtual teams and can motivate others effectively.</p></li><li><p>Possess an excellent understanding of cross-functional activities and their intersections with External Data.</p></li><li><p>Manage multiple priorities with attention to detail and deliver results within tight timelines.</p></li><li><p>Communicate effectively through strong interpersonal, oral, and written skills.</p></li><li><p>Adapt quickly in a fast-paced, dynamic environment.</p></li><li><p>Are open to travel up to 20%.</p></li></ul><p><strong>To be qualified for this role, you must meet the following requirements:</strong></p><ul><li><p>A minimum of <strong>10+ years of experience</strong> in External Clinical Data Management, with expert knowledge of database structures in biotechnology, pharmaceutical, or health-related industries.</p></li><li><p>At least <strong>4 years of people management experience</strong>.</p></li><li><p>A <strong>Bachelor’s degree</strong> in Science, Health, Computing, or a related field.</p></li><li><p>Hands-on experience with <strong>Imaging Data</strong> is required.</p></li><li><p>Advanced knowledge of <strong>Biomarker data types</strong> and/or Imaging Data for oncology and non-oncology studies is a plus.</p></li><li><p>Expert knowledge of database structures is preferred.</p></li></ul><p>This role is ideal for a seasoned professional who thrives at the intersection of leadership, technical expertise, and strategic vision. If you’re ready to make a significant impact in External Data Services, this position could be your next career milestone.</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>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 11:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Product Management, Delivery & Operations]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45153]]></requisitionid>
    <referencenumber><![CDATA[R45153]]></referencenumber>
    <apijobid><![CDATA[r45153]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45153/director-product-management-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>The Global Development IT Director, Product Management is a key member of the GDIT Delivery & Operations organization, responsible for overseeing and guiding their team members in delivering, maintaining & enhancing all technology products in their defined business domain. This resource will also partner with key business stakeholders to intake, design, implement and enhance technology products. This role will work closely with Business Solution Partners (BSP) to deliver projects and technology product improvements. The role will also be responsible for line management of product owners aligned to the domain and will assume product owner responsibilities for a specific set of technologies, including end-to-end implementation and support for all products that fall within the domain. This role will be responsible for the Development Operations & Portfolio Management (DO&PM) domain. </p><p><em><strong>The role will be based onsite at our offices in Warren, NJ or Armonk, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><strong>In this role, a typical day might include the following:</strong></p><div><ul><li><p>Lead & coach the Product Leads and Product Analysts within GDIT Delivery & Operations assigned to the domain, ensuring delivery on team commitments, collaboration across members, and definitions of processes, tools and competencies needed to further build the domain capabilities. </p></li></ul></div><div><ul><li><p>Oversee all operational support for products and domain providing line leadership and guidance to individual product owners while thinking across product lines. </p></li></ul></div><div><ul><li><p>Ensure alignment with product model processes and standards while customizing to meet domain-specific needs as applicable, including being responsible for product backlog and incidents management, including insights into enhancements and incidents trends over time. </p></li></ul></div><div><ul><li><p>Partner with the Business Process Owners and BSPs to implement new/enhanced technologies, and take ownership of products including end-to-end support, performance, and commitment to continuous improvement. </p></li></ul></div><div><ul><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></ul></div><div><ul><li><p>Responsible for identifying resourcing needs and for oversight of internal and vendor delivery, and managed service vendor associates in support of product. </p></li></ul></div><div><ul><li><p>Work collaboratively with GDS functions, Corporate IT, and other relevant functions in the management of enterprise systems, including development and adherence to standards and governance. </p></li></ul></div><p><strong>This Job Might Be For You If You Have:</strong></p><div><ul><li><p>Proven ability to manage competing priorities across a multitude of stakeholders and to direct teams to deliver value-oriented, prioritized solutions. </p></li></ul></div><div><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></ul></div><div><ul><li><p>Strong record of accomplishment in technology project management, stakeholder management, budget management and value engineering. </p></li></ul></div><div><ul><li><p>Ability to effectively manage multiple priorities with a sense of urgency, and effectively manage ambiguity and changing priorities </p></li></ul></div><div><ul><li><p>Experience managing technology capability identification, selection, implementation, and operations </p></li></ul></div><div><ul><li><p>Excellent problem-solving skills to address day-to-day challenges associated with business solutions </p></li></ul></div><div><ul><li><p>Knowledge of pharmaceutical Global Development business capabilities, processes, systems, and key trends in the industry. </p></li></ul></div><div><ul><li><p>Experience growing and motivating a team, coaching members through career milestones and progression. </p></li></ul></div><div><ul><li><p>Exposure to delivering presentations and engaging with senior leadership. </p></li></ul></div><p><strong>To be considered for this role, you must have:</strong></p><div><ul><li><p>BS/BA Degree with 12+ years relevant experience </p></li></ul></div><div><ul><li><p>MS Degree with 10+ years relevant experience </p></li></ul></div><div><ul><li><p>Deep knowledge of Development Operations & Portfolio Management business processes, including but not limited to Drug Development Program and Portfolio Management; Resource Management; Clinical Trial Feasibility, Planning, Execution, and Closeout; Clinical Monitoring; Study Start-up; Site Management; and Clinical Drug Supply Management. </p></li></ul></div><div><ul><li><p>Experience managing technology teams and driving business value in the Clinical Operations space with specific technologies like Veeva Clinical Vault (CTMS, TMF, SSU, etc.), CluePoints, Planisware, etc., a plus. </p></li></ul></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[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 12:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[IT Lead, Manufacturing GxP]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46064]]></requisitionid>
    <referencenumber><![CDATA[R46064]]></referencenumber>
    <apijobid><![CDATA[r46064]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46064/it-lead-manufacturing-gxp/]]></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>We are seeking a skilled IT professional to serve as the IT Lead for Regeneron's Cell Medicines (RCM) Manufacturing operation to support and maintain all Clinical Manufacturing Equipment and data acquisition/monitoring systems. This role will require strong management skills to effectively manage the support needed from multiple Regeneron Corporate IT services groups and external support vendors as needed, in addition to strong technical skills as the primary On-Site IT SME for the Clinical Manufacturing area.</p><p>This individual will ensure seamless communication, service delivery, and networking of points of contact across multiple IT groups and the business. The ideal candidate will have leadership and communication skills, experience in a GMP (Good Manufacturing Practices) environment, and the ability to troubleshoot on-site IT issues related to all Manufacturing and QC equipment and facilities IT systems.</p><p><strong>As an IT GxP Manufacturing Lead, a typical day may include: </strong></p><ul><li><p>Serve as the primary point of contact between RCM and Corporate IT, coordinating support across internal groups and external vendors.</p></li><li><p>Align IT services with RCM’s needs by facilitating clear stakeholder communication on requirements, timelines, and deliverables.</p></li><li><p>Lead planning and execution of IT projects and initiatives within a GMP environment, ensuring effective cross-team coordination.</p></li><li><p>Provide regular operational and project status updates, metrics, and risk/issue reports to leadership.</p></li><li><p>Manage and direct contracted IT personnel and oversee vendor performance for service delivery.</p></li><li><p>Troubleshoot and resolve on-site IT issues for manufacturing, QC equipment, and facilities systems (hardware/software), ensuring rapid restoration.</p></li><li><p>Ensure high availability and resilience of critical systems through monitoring, preventive maintenance, backups/archiving, and recovery readiness.</p></li><li><p>Develop and maintain GxP documentation, including specifications, test protocols, validation/CSV records, and system administration SOPs.</p></li><li><p>Support integration of equipment and systems with LIMS and other enterprise platforms in coordination with Corporate IT; supervise EMS for compliance and reliability.</p></li><li><p>Ensure GMP/regulatory compliance by partnering with QA, managing IT tasks in CMMS, maintaining audit readiness, and driving continuous improvement of workflows and support processes.</p></li></ul><p><strong>This role could be for you if you: </strong></p><ul><li><p>Strong management and leadership abilities.</p></li><li><p>Excellent written and verbal communication skills.</p></li><li><p>Ability to collaborate effectively with cross-functional teams.</p></li><li><p>Proven track record of collaborating with corporate IT teams.</p></li><li><p>Ability to adapt to a fast-paced, multifaceted work environment.</p></li></ul><p><strong>To be considered for this role, you must meet the following:</strong></p><ul><li><p>Bachelor’s degree in information technology, Computer Science, or a related field.</p></li><li><p>5 – 10 years' demonstrated ability in an IT role, preferably within a GMP-regulated environment.</p></li><li><p>Proficiency in troubleshooting all IT aspects of manufacturing/QC equipment and other data collection/monitoring systems (e.g. EMS)</p></li><li><p>Familiarity with GMP requirements and IT compliance standards.</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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Software Engineer]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43915]]></requisitionid>
    <referencenumber><![CDATA[R43915]]></referencenumber>
    <apijobid><![CDATA[r43915]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43915/principal-software-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>The Regeneron Genetics Center is one of the largest human genetics sequencing programs in the world. We study human DNA at massive scale to understand why diseases happen and how we can stop them. Using genetics to improve human health, our research has contributed directly to medicines helping patients today.</p><p>The RGC IT team builds and maintains shared services, platform tooling, and APIs that our research teams depend on. We approach development with an AI-first mindset, utilizing LLM-powered tooling to move faster, explore more ideas and quickly turn complex problems into working solutions for our scientists.</p><p><strong>A Typical Day As a Principal Software Engineer, you’ll contribute to:</strong></p><ul><li><p>API and service development across a shared platform that research teams use to access and work with large-scale genetic data.</p></li><li><p>Cloud-based data pipeline work on AWS, keeping high-volume genomic data moving reliably and performantly.</p></li><li><p>Integrating and applying AI tooling across development workflows — from LLM-assisted coding and review to building AI-powered capabilities into the platform itself.</p></li><li><p>Working directly with scientists and engineers to understand requirements and deliver meaningful solutions to improve our scientific discovery process.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Strong fundamentals at the API and data layer. You’ve built production APIs, integration services, and pipelines in the cloud as microservices.</p></li><li><p>Comfortable with AI-first development. You use tools like Claude Code as a core part of how you work — not occasionally, but throughout planning, implementation, and review.</p></li><li><p>Technical depth across the stack. API design patterns, distributed systems, cloud-native development on AWS — you can contribute without needing everything handed to you.</p></li><li><p>Works well as part of a team. Decisions here are collaborative. You do good work in that kind of environment.</p></li><li><p>Takes quality seriously. You write things that can be tested and maintained, and you know why that matters at scale.</p></li></ul><p><strong>To be considered for this opportunity,</strong> you must have a Bachelor’s Degree or higher with at least 6 years of relevant IT experience building cloud-native applications. Candidates must have hands-on experience with:</p><ul><li><p>Languages & Runtimes: Python, TypeScript</p></li><li><p>API & Integration: REST API design and development, service integration patterns</p></li><li><p>AI Tooling: LLM-assisted development tools (e.g. Claude Code, GitHub Copilot), AI/ML service integration</p></li><li><p>Data & Databases: PostgreSQL or MySQL, Redshift or Snowflake, ETL orchestration</p></li><li><p>Infrastructure: Docker, AWS cloud services</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr Global Trial Optimization]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45491]]></requisitionid>
    <referencenumber><![CDATA[R45491]]></referencenumber>
    <apijobid><![CDATA[r45491]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45491/sr-mgr-global-trial-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Global Trial Optimization will lead program or study level activities advising on our clinical development strategy, clinical study concepts, study protocols and operational plans that will enable predictable delivery of clinical programs and studies. You will develop and maintain relationships with our external experts facilitating a wide source of country and disease area intelligence used in study design and operational planning. </p><p><strong>A typical day may include the following: </strong><br>• Lead study level feasibility processes to generate high quality and timely data to inform study design, efficient geographical placement and operational planning.<br>• Partner with teams during CRO led feasibility activities supporting validation of study and country level enrollment rates and study start up timelines to advise budget and baseline setting.<br>• Supports the development and implementation of the Global Trial Optimization function through process initiatives and change management. <br>• Partner with Data and Analytics function to review and identify appropriate central data sources. <br>• Articulate the data story to teams based on country level feasibility and centrally derived data to support data driven decisions to improve protocol design<br>• Project management of study level country landscape assessment activities and the collection of targeted feasibility information for early assessment of operational feasibility for conducting clinical trials.<br>• Lead study level engagements to acquire, analyze and deliver high quality targeted information from external partners. <br>• Prove input into continuous improvement activities to ensure consistency of process execution.<br>• In partnership with Clinical Outsourcing provide functional input into the identification, qualification and relationship management of a range of vendors.<br>• Develop and implement patient recruitment and retention tactics aligned with defined study strategy.<br>• Develop and maintain knowledge of external clinical trial environment and assess developments for impact on study design and execution<br>• May require up to 20% travel</p><p>To be considered a Bachelors degree in a related field with a minimum of 8 years of relevant industry experience within pharma/biotech, a CRO or consulting is required. Strong understanding and experience in operationalizing clinical development programs in a global setting from first-in-human to post-approval. Experience with feasibility. Must be a compelling communicator with ability to translate sophisticated messages to a variety of audiences.<br>Additional requirements include: <br>• Experience in using data to inform clinical strategy development<br>• Ability to understand sophisticated business questions and develop effective solutions<br>• Experience in process development, implementation and change management activities<br>• Line management experience preferred<br> </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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Site Start Up Lead]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46032]]></requisitionid>
    <referencenumber><![CDATA[R46032]]></referencenumber>
    <apijobid><![CDATA[r46032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46032/senior-manager-global-site-start-up-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>he <strong>Senior Manager, Global Site Start-Up Lead </strong>(SSU Lead) is responsible for driving the global execution of site activation for complex, high profile clinical trials, performing the role with high-degree of independence to ensure efficient and compliant processes aligned with Regeneron SOPs, ICH-GCP guidelines, and industry standards. Partnering closely with cross-functional teams and Clinical Research Organizations (CROs), this role balances strategic oversight with hands-on leadership to address challenges and deliver study objectives. The SSU Lead develops site activation projections, mitigates risks impacting site activation, and monitors CRO performance by analyzing metrics. Additionally, they lead all aspects of site start-up activities, including fast-track initiation, milestone tracking, and document collection, while ensuring timely submissions and leveraging country intelligence for informed decision-making. This person will also be responsible for direct line management and supporting development of their team.<strong> </strong></p><p><strong>A typical day in this role looks like: </strong></p><p>Site Start-up Strategy </p><ul><li><p>Develop the site start up strategy for each study assigned (complex, high profile), outlining all dependencies impacting site activation and actively mitigating and escalating risks. </p></li><li><p>Oversee the tracking and analysis of study metrics, including risks and mitigation strategies and to evaluate CRO performance and implement corrective actions.</p></li><li><p>Advocate for optimized site selection strategies, leveraging data-driven insights to guide cross-functional teams toward effective decision-making.</p></li><li><p>Lead the development, assessment, and alignment of site activation projections, ensuring cross-functional and CRO collaboration to meet strategic objectives.</p></li><li><p>Ensure comprehensive and compliant documentation of site start-up materials in the Trial Master File (TMF) to maintain inspection readiness.</p></li></ul><p>Country Start-up </p><ul><li><p>Partner with cross functional and CRO partners (where applicable) to develop a comprehensive global country start up strategy, outlining all dependencies impacting country start up and actively mitigating and escalating risks cross functionally. </p></li><li><p>Monitor and maintain country intelligence data to support informed decision-making and develop accurate startup projections and strategic plans.</p></li><li><p>Support regulatory submissions as needed, including activities such as: providing required site documentation, coordinating submissions to Central Institutional Review Boards (CIRBs), supporting sites with Local Institutional Review Board (LIRB) submissions, and handling or supervising Clinical Research Organization (CRO) insurance requests, etc.</p></li><li><p>Ensure timely country submission deliverables (ensure task completion; all roles clarity, identification of critical path items, effective communication pathway). </p></li></ul><p>Site Start up Management</p><ul><li><p>Lead and oversee all aspects of site start-up activities for complex, high profile studies, including fast-track site initiation, site calls, document collection, and milestone tracking, ensuring timely and efficient completion of processes.</p></li><li><p>Serve as the subject matter expert for essential site documents, providing training, guidance, and support to teams and sites on regulatory requirements, document management, and TMF filing.</p></li><li><p>Oversee CRO site start up management or in house site facing regional SSU team, where applicable</p></li><li><p>Lead the collection and analysis of site intelligence to support strategic site selection and site start-up.</p></li><li><p>Oversee the preparation and approval of site regulatory package, ensuring compliance with country-specific requirements, TMF standards, and ICH-GCP guidelines, while supporting inspection readiness and maintaining high-quality site documentation.</p></li></ul><p>Team Interactions</p><ul><li><p>Represent SSU on cross-functional teams, providing updates, escalating challenges, and proposing mitigation strategies for site start-up issues.</p></li><li><p>Act as the escalation point for CRO and internal team to ensure timely SSU issue resolution </p></li></ul><p>Process Improvement</p><ul><li><p>Recommends and drives cross functional and department process improvements.</p></li></ul><p>Line Management</p><ul><li><p>Responsible for direct supervision of SSU staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require up to 25% travel</p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Strong interpersonal and leadership skills</p></li><li><p>Ability to provide and implements operational strategic direction and guidance for respective clinical trials</p></li><li><p>Demonstrates strong knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Strong communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Ability to lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Strong technical proficiency in trial management systems (CTMS, TMF) and MS applications including (but not limited to) Project, PowerPoint, Word, Excel</p></li><li><p>Extensive experience in the clinical drug development process, including study start-up</p></li><li><p>Knowledge and understanding of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Strong project management skills, cross-functional team interaction and organizational skills</p></li><li><p>Line management experience preferred</p></li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree and 8+ years of relevant industry expereince is required. Preference in a sponsor Site Start-Up role preferred.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 07:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager External Bulk Manufacturing]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45691]]></requisitionid>
    <referencenumber><![CDATA[R45691]]></referencenumber>
    <apijobid><![CDATA[r45691]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45691/manager-external-bulk-manufacturing/]]></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 fill a Mgr External Bulk Manufacturing position. The Mgr External Bulk Manufacturing strategically manages business relationships and/or facilitates day-to-day operations with Contract Manufacturing Organizations (CMOs) and Partners to achieve a consistently high level of interaction in order to meet or exceed Regeneron’s business needs relating to product quality, availability and delivery. Ensures that all critical external bulk manufacturing requirements are executed to ensure world-class performance of Industrial Operations & Product Supply (IOPS) product supply chains. The role of the Manager External Bulk Manufacturing is to act as the Relationship Lead with the CMO/Partners.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Ensures that product manufacture occurs in compliance with cGMP and applicable regulations.</p></li><li><p>Facilitates all External Bulk Manufacturing activities at contract and/or business partner manufacturing sites, including but not limited to scheduling of all batches, supply of materials, direct shipment of bulk and finished product at manufacturing site, tracking and monitoring cycle times and providing any required associated reports and technical expertise.</p></li><li><p>Forms strategic partnerships with technical and operational colleagues to effectively collaborate with other departments and contractors.</p></li><li><p>Functions as a liaison between Regeneron Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners.</p></li><li><p>Ensures the timely routine and review of all technical transfer activities, validation plans, master manufacturing records (MRs), standard operating procedures (SOPs) and other documentation needed to successfully execute required clinical and commercial external manufacturing activities at contractors and/or business partners.</p></li><li><p>Supports and informs strategic initiatives and contract negotiations that drive long-term relationship stability and success.</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>The Relationship Leads manage quarterly business review meetings or other governance structures with CMOs to drive continuous improvement in joint performance.</p></li><li><p>Resolves all supply issues with the CMO/Partner that affect product quality or availability, including evaluating cost/benefit scenarios, making sound recommendations and coordinating internal and external resources to address issues.</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>The Relationship Leads have overall responsibility for RFPs, project plans, purchase requisitions, etc. associated with contractor operations.</p></li><li><p>Provides regulatory filing support to IND, BLA, MAA, etc.</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><li><p>May manage direct report and/or lead a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.</p></li><li><p>May serve as the primary Regeneron technical contact for select contract manufacturing sites concerning day-to-day activities.</p></li><li><p>Travels to contract manufacturers or business partners, as required (25-50%).</p></li></ul><p>To be considered for the Associate Manager you must have a BS/BA in business or scientific discipline and 6 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</p><p>To be considered for the Manager you must have a BS/BA in business or scientific discipline and 7 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</p><p>To be considered for the Senior Manager you must have a BS/BA in business or scientific discipline and 8 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</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>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 17:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Oncology Lung Cancer Marketing]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46333]]></requisitionid>
    <referencenumber><![CDATA[R46333]]></referencenumber>
    <apijobid><![CDATA[r46333]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46333/director-us-oncology-lung-cancer-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[<p>The Director, US Oncology HCP Lung Cancer Marketing, is a member of the Oncology Business Unit with accountability for working closely with the Senior Director to develop commercial HCP promotion strategy and tactical plans for Non-Small Cell Lung Cancer (NSCLC) within the US. Also responsible for collaborating with the International team for Global commercialization and promotion.</p><p>This position will report directly to the Senior Director, US HCP Lung Cancer Marketing. The Director will work collaboratively across the Franchise Team, International teams, internal cross-functional colleagues, while effectively managing external agency partners to ensure alignment and to drive optimal integration and execution of personal and non-personal initiatives.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Lead HCP marketing for the NSCLC indications in the US. This includes defining US market opportunities, analyzing the competitive landscape, identifying key site of care and key account segmentation and needs, developing customer-focused and differentiated product and indication positioning, and customizing messages to key target audiences.</li><li>Works in close collaboration with Clinical, Medical Affairs and Field Medical to ensure alignment with Medical Education strategic plans.</li><li>Engage with physician experts and attend key congresses to support Scientific Marketing team efforts and assess important disease and treatment data.</li><li>Work closely with the Insights and Data Analytics team to design and implement promotional strategies, while tracking brand performance, share of voice, market dynamics and competitive actions & response. Provide business assumptions input to forecasting.</li><li>Oversee and collaborate with Digital/Media Strategy team for optimization and implementation of the multi-channel marketing mix, including omni-channel digital & media strategy and implementation, and creation and deployment of educational resources towards brand objectives and developing indicators/metrics for high-impact engagements with HCP key target audiences.</li><li>Develop and coordinate NSCLC HCP Marketing inputs and key sections of brand plan, identify and prioritize business opportunities.</li><li>Responsible for the development of the Field Plan of Action and training plan, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/collaborators.</li><li>Maintain strong collaborative relationships with cross-functional areas and internal strategic partners (i.e., Field Sales, Training, Promotional Review Committee, Medical Affairs, Regulatory, Clinical, Legal, Compliance, Market Access etc.)</li><li>Ensures that the marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines.</li><li>Manages and develops a direct report to ensure their continued development and growth.</li><li>Works cross functionally to create, manage and track budget to ensure operating within the approved budget and phasing.</li></ul><h3><strong>This job might be for you if:</strong></h3><ul><li>You are effective collaborator and communicator both written and verbal</li><li>You can navigate regularly in ambiguity</li><li>You excel in a fast paced environment</li></ul><p>To be considered for this role, we expect you to have a Bachelors degree is required; 12+ years of pharmaceutical marketing focused on Oncology. Along with leading and developing long range brand plans, budgets and forecasts for commercial teams in the pharmaceutical/biotech industry. Lastly, this role requires you to travel 30% of the time and to be in the office in Sleepy Hollow, NY 4 days a week.</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, HR Business Partner]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45764]]></requisitionid>
    <referencenumber><![CDATA[R45764]]></referencenumber>
    <apijobid><![CDATA[r45764]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45764/senior-manager-hr-business-partner/]]></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>Regeneron is seeking a Senior Manager, HR Business Partner (HRBP) to support the Regeneron Genetics Center (RGC) and Translational Medicine business units. This role will report into the Senior Director, HR Business Partner.</p><p><em><strong>This role is based at our Global HQ in Tarrytown, NY with a minimum of 4 days onsite required - this is not open to remote / hybrid work.</strong></em></p><p>At Regeneron, an HRBP develops solutions to solve business challenges in order to increase their ability to deliver on our mission - utilizing science to bring new medicines to patients. You will be partnering with other HRBPs, COE functions within HR, and other key stakeholders to provide support and counsel to the business managers / employees on organizational and people related issues. This will include talent acquisition & planning, onboarding and development, employee engagement, culture, performance management, and change management to promote and maintain REGN’s high-performance culture, the Regeneron Way.</p><p>Key to this will also be your ability to quickly develop trusted relationships with people at all levels within the RGC and Translational Medicine as well as a strong partnership with your Sr. HRBPs and COE partners. You have to be comfortable with challenging the status quo, influencing scientifically trained leaders and delivering key HRBP support in a fast-paced culture. Being able to pivot is key. This role acts as a champion and a coach for our expanding business.</p><p><br><strong>As a Senior Manager, HRBP a typical day may include:</strong></p><ul><li>Partnering with the HRBP Leadership to identify and plan key HR work for the business functions. This role works across all client groups. </li><li>Working with managers and employees to help solve any employee relations, people related challenges, keeping in mind precedence and business needs including partnering with internal HR specialists </li><li>Handling conflicts, investigations, and employee grievances</li><li>Providing coaching to managers and employees with an emphasis on helping the person understand what their options are for each situation and how to demonstrate the Regeneron Way</li><li>Participating in interviews for key positions, as well as candidate debriefs to help drive the best hiring decisions in a rapidly expanding organization </li><li>Onboarding new managers by partnering with hiring managers to facilitate and support a successful onboarding experience </li><li>Identifying needs (individual and team) within client areas and partner with the OD Consulting team to craft solutions that will address business needs (e.g., team building)</li><li>Partnering with Total Rewards to define new roles, identify external comparable/market value of positions and other reward/recognition programs </li><li>Partnering with managers to support year-end performance calibrations as well as year-end compensation in Workday</li><li>Ad hoc project support (e.g., career ladders, re-organization projects)</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Are able to quickly develop trusted relationships with peers and employees at all levels</li><li>Are comfortable with challenging the status quo in a growing team and influencing scientific and technical leaders</li><li>Are learning agile and comfortable with a high level of ambiguity</li><li>Have strong analytical skills and you use data to identify problems and deliver solutions that will benefit employees</li><li>Have exceptional employee relations skills and experience</li></ul><p><strong>To be considered for this role you must possess a Bachelor’s degree in a scientific or HR related discipline; advanced degrees such as MBA, or Master’s in OD / IO or Human Resources is preferred. Minimum of 10-12 years’ HR experience, with experience working within the pharma/biopharma/biotech or Manufacturing industry highly preferred.</strong></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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, MES Implementation & Integration]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43089]]></requisitionid>
    <referencenumber><![CDATA[R43089]]></referencenumber>
    <apijobid><![CDATA[r43089]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43089/director-mes-implementation-integration/]]></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>The Director of MES (Implementation and Integration) will drive the end-to-end implementation of Manufacturing Execution Systems (MES) across our biopharmaceutical facilities. You will develop and implement integration architectures connecting MES with Ignition, DeltaV, and Rockwell platforms, ensuring seamless deployment across retrofitted and future facilities while modernizing workflows to meet regulatory and operational standards.</p><p>As a Director, MES Implementation & Integration, a typical day might include the following:</p><ul><li>Contribute to the strategic vision of MES and lead the implementation and integration of the MES system across all manufacturing sites, while developing strong business relationships with stakeholder groups to attain a solid understanding of their goals and objectives.</li><li>Develop tailored frameworks for MES integration with Ignition plant hubs, DeltaV control systems, and Rockwell HMI platforms, addressing distinct technical paradigms rather than unified strategies.</li><li>Establish master data architecture frameworks to enable system deployment, ensuring validation and regulatory compliance across FDA-regulated environments.</li><li>Manage complex validation requirements and change control processes while transforming paper-based batch records into compliant digital workflows.</li><li>Diagnose and resolve integration challenges, including connectivity issues between disparate automation platforms, while maintaining quality and timeline constraints.</li><li>Redesign workflow processes to leverage integrated system capabilities, optimizing operational efficiency and regulatory readiness.</li><li>Provide MES team members with mentorship and support to ensure that they have the skills and tools required to consistently support business needs and individual professional goals.</li></ul><p>This role may be for you if you have:</p><ul><li>Comprehensive understanding of biopharmaceutical manufacturing processes, batch record requirements, validation standards, and change control procedures within FDA-regulated environments.</li><li>Experience managing process digitization initiatives that maintain regulatory compliance while enabling operational efficiency improvements through integrated system capabilities.</li><li>Deep expertise addressing integration challenges across different automation platforms and system architectures. Proven ability diagnosing complex technical problems and implementing solutions under timeline pressure while maintaining quality and compliance standards.</li></ul><p>In order to be considered for this position, you must hold a BS degree in a life sciences, computer science or engineering discipline or related field and</p><ul><li>Associate Director: 10+ of pharmaceutical/biotechnology industry experience</li><li>Director: 12+ years of pharmaceutical/biotechnology industry experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</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>$145,600.00 - $282,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 09:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Veterinary Services]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43495]]></requisitionid>
    <referencenumber><![CDATA[R43495]]></referencenumber>
    <apijobid><![CDATA[r43495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43495/senior-manager-veterinary-services/]]></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>Regeneron's Veterinary Services group, located in Tarrytown, NY is seeking a Manager. In this exciting role, you will assist the Executive Director and Director in administering a program of animal care and use for animal research and production facilities. Core responsibilities include managing the laboratory animal facility and providing oversight of daily operations in conjunction with Vivarium Operations personnel.</p><h3><strong>A Typical Day in the Role of Manager Might Look Like: </strong></h3><ul><li>Maintains Vivarium to inspection- ready condition at all times.</li><li>Ensures staffing levels are appropriate to ensure proper care and compliance with department Standard Operating Procedures and policies.</li><li>Advises workers regarding requirements for compliance with safety, and state and federal guidelines for operation of research facility.</li><li>Monitors care and health of animals.</li><li>Provides input with respect to hiring personnel and performance evaluations.</li><li>Reassigns team to other assignments based on staffing needs.</li><li>Teaches workers regarding procedures, such as feeding and cleaning schedules and documentation.</li><li>Reviews work of personnel to determine established procedures are followed and to verify accuracy of documentation.</li><li>Maintains accurate records and inventories related to supplies, equipment, and receipt and assignment of animals.</li><li>Supervises and coordinates activities of workers involved in operations of animal research facility: arranges purchase of items, such as animal feed, bedding, and supplies.</li><li>Oversees the animal care facility by providing work direction to Vivarium Operations staff</li><li>Conducts inspections of animal facilities to ensure the maintenance of required sanitation standards; observe and report noticeable or unusual changes in animals.</li><li>Collaborates on the development of animal care facilities processes and policies.</li><li>Provides input and writes initial performance evaluations for assigned staff. Provides input into hiring, termination and disciplinary actions for team.</li><li>Maintains facility documentation and tracking reports as necessary</li><li>ACLAM board eligible</li></ul><h3>The Role Might Be For You If You Have:</h3><ul><li>Extensive knowledge and technical proficiency in standard laboratory animal techniques</li><li>Extensive knowledge of laboratory animal medicine</li><li>Knowledge of applicable regulations regarding the proper standards of animal care and use in a research environment.</li></ul><p>This role requires a minimum of 7+ years of relevant experience with rodents and rabbits in a laboratory setting is required for this position. This position requires a DVM or equivalent degree. Biotech experience preferred.</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Review Committee Specialist]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44924]]></requisitionid>
    <referencenumber><![CDATA[R44924]]></referencenumber>
    <apijobid><![CDATA[r44924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44924/senior-review-committee-specialist/]]></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 believe that when the right idea finds the right team, powerful change is possible. Join our dynamic Commercial Operations team as a Senior Specialist, Review Committee. In this pivotal role, you will lead and coordinate promotional review activities, ensuring compliance, efficiency, and excellence in all processes. This is your chance to create a significant impact by contributing to the success of multiple therapeutic areas while working in a collaborative and innovative environment. This is a hybrid role, onsite requirement is 4 days per week.</p><div></div><div><p><strong>A Typical Day:</strong> </p></div><div><ul><li><p>Guide promotional material sponsors through review cycle timelines, from submission to approval. </p></li></ul></div><div><ul><li><p>Review promotional materials for accuracy, ensuring compliance and routing submissions appropriately. </p></li></ul></div><div><ul><li><p>Facilitate and lead Review Committee meetings to maintain adherence to policies and procedures. </p></li></ul></div><div><ul><li><p>Coordinate submissions of promotional materials to the FDA Office of Prescription Drug Promotion (OPDP) as required. </p></li></ul></div><div><ul><li><p>Oversee planning and prioritization for FDA approvals and label updates for assigned brands. </p></li></ul></div><div><ul><li><p>Monitor performance and compliance metrics, advising on process improvements. </p></li></ul></div><div><ul><li><p>Support training initiatives and recommend enhancements to platforms like PromoMats. </p></li></ul></div><div><ul><li><p>Foster partnerships and shared accountability across stakeholders, including reviewers, sponsors, and agencies. </p></li></ul></div><div><p><strong>This Role May Be For You If:</strong> </p></div><div><ul><li><p>You have a strong customer service ethic and excel in building relationships with management, customers, vendors, and partners. </p></li></ul></div><div><ul><li><p>You thrive in a detail-oriented role and are skilled in problem-solving and conflict resolution. </p></li></ul></div><div><ul><li><p>You are familiar with the drug development and commercialization process and have experience working across multiple therapeutic areas. </p></li></ul></div><div><ul><li><p>You enjoy managing high-quality committee meetings and ensuring compliance with all laws, policies, and procedures. </p></li></ul></div><div><p><strong>To Be Considered:</strong> </p></div><div><p>To qualify, you must hold a Bachelor’s Degree and have 5–7 years of related promotional review experience, preferably in advertising, medical education, or the pharmaceutical industry. Experience managing Medical, Legal, and Regulatory (MLR) review committees is essential, as is experience with co-promote brands. A certificate in Project Management is a plus. </p></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>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 10:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Associate Director Medical Communications]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45910]]></requisitionid>
    <referencenumber><![CDATA[R45910]]></referencenumber>
    <apijobid><![CDATA[r45910]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45910/temporary-associate-director-medical-communications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>We are Regeneron, a company dedicated to transforming lives through innovative medical solutions. We are seeking an Associate Director, Medical Communications to join our team in Spain. In this role, you will play a pivotal part in shaping scientific communication strategies and providing expert medical information to diverse collaborators. Initially focusing on Oncology, your work will directly contribute to advancing healthcare and improving patient outcomes. This is a temporary role for 8 months. </p></div><div><p><strong>A Typical Day:</strong> </p></div><div><ul><li><p>Strategize and implement scientific communication needs in Spain, aligning with global medical strategies. </p></li></ul></div><div><ul><li><p>Develop and maintain high-quality medical information response documents, product dossiers, and scientific Q&As. </p></li></ul></div><div><ul><li><p>Provide scientific and medical review of medical and promotional materials to ensure accuracy and compliance. </p></li></ul></div><div><ul><li><p>Collaborate with the Medical Director, Field Medical, brand teams and Global Medical Affairs to create a unified approach for external engagement </p></li></ul></div><div><ul><li><p>Be part of the European team for Global Medical Communications, with colleagues located in the main European countries </p></li></ul></div><div><ul><li><p>Identify and coordinate scientific communication opportunities at national and local congresses, including presenting meaningful data. </p></li></ul></div><div><ul><li><p>Analyze and provide insights from country-specific analytics, call volumes, and case data. </p></li></ul></div><div><p><strong>This Role May Be For You If:</strong> </p></div><div><ul><li><p>You have a strong background in scientific communications and medical information. </p></li></ul></div><div><ul><li><p>You excel at working collaboratively across global teams and forming effective partnerships. </p></li></ul></div><div><ul><li><p>You are detail-oriented and skilled at developing impactful communication strategies using traditional and digital methods. </p></li></ul></div><div><ul><li><p>You thrive in a role that blends strategic planning with operational execution </p></li></ul></div><div><ul><li><p>You are fluent in English. </p></li></ul></div><div><p><strong>To Be Considered:</strong> </p></div><div><p>Applicants should possess a PhD, PharmD, or MD, along with at least five years of experience in scientific communications and two years in medical information. A strong understanding of the Spanish healthcare regulatory environment is important. Prior experience in the biotech or pharmaceutical industry, particularly in Medical Affairs or Clinical Research & Development, is highly desirable. This position will involve 25% travel to attend medical congresses and engage with stakeholders. </p></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Sr Payroll Analyst]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46044]]></requisitionid>
    <referencenumber><![CDATA[R46044]]></referencenumber>
    <apijobid><![CDATA[r46044]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46044/temp-sr-payroll-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role, you will report to the Payroll Manager. The Payroll Analyst will support the wider team in the completion of all payroll tasks.</p><p>This is a 12 month temporary contract. </p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li>Reviewing and inputting all administrative payroll data changes to records for processing of our bi- weekly and monthly payroll and maintain records</li><li>Working with other departments such as Comp & Bens and HRPB’s to ensure payroll data is correct and processed accordingly</li><li>Reconciling each payroll, reviewing all entries and forward for approval</li><li>Ensuring accuracy in all tax information, reconciliations and payments</li><li>Undertaking Time & Labour processing and administration of time cards</li><li>Managing the internal inbox with responsibility for responding to employees’ queries</li><li>Assisting with audit queries related to payroll</li><li>Updating SOPs and training documents for a variety of payroll processes</li><li>Working with the team to evaluate and test system enhancements to Core Pay</li></ul><p><strong>This role might be for you if you have: </strong></p><ul><li>A positive can do approach to work</li><li>A proven track record at completing projects and assigned tasks</li><li>Experience in European payroll (preferred but not required)</li><li>Strong Excel experience including Pivot Tables, VLookups and Macros</li></ul><p>To be considered for this role you should have an IPASS qualification with a minimum of 5 years’ experience in a high-volume environment and years’ experience with Core Pay and Core Insight. Experience in Oracle and Workday preferred but not required.</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 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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44657]]></requisitionid>
    <referencenumber><![CDATA[R44657]]></referencenumber>
    <apijobid><![CDATA[r44657]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44657/manager-internal-medicine-clinical-scientist-immuneinflammatory/]]></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>We are seeking a Manager, Clinical Scientist to join our team. The Manager Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Manager works in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to the Associate Director/Director Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p></div><div><div><div><div><div><div><div><div><p><strong>As a Manager within Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings</p></li><li><p>May contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments</p></li><li><p>Develops/maintains basic 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 limited knowledge of disease and drug landscape</p></li><li><p>Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets</p></li><li><p>May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborate with others for scientific and foundational guidance</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)</p></li><li><p>Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Supports identification of data trends and potential inconsistencies in data across assigned studies and raises</p></li><li><p>Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>Demonstrated basic knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills</p></li><li><p>Demonstrate some ability to influence within study team</p></li><li><p>Independently resolves most issues and complex matters, requiring advanced analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven track record in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related area. Additionally, ≥ 6 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in immune/inflammatory related clinical trials. Basic knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p></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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 11:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HR Manager, Employee Relations]]></title>
    <date><![CDATA[Sun, 16 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43595]]></requisitionid>
    <referencenumber><![CDATA[R43595]]></referencenumber>
    <apijobid><![CDATA[r43595]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43595/hr-manager-employee-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>The HR Employee Relations Manager will conduct sophisticated investigations, provide advice and direction regarding employee and labor relations matters to HR key stakeholders, business executives, managers, and employees across the organization. This is an opportunity to help build and shape the ER function for a company that is growing - in size, complexity and world-wide impact. Our centralized ER function is a new and highly-respected team that is setting the course for how employee relations works with and influences the organization.</p><p><strong><em>This role is based at our Sleepy Hollow, NY </em><em>location </em><em>with a minimum of 4 days onsite required - this is not open to fully remote or hybrid work.</em></strong></p><p><strong>As an Employee Relations Manager, a typical day may include: </strong></p><ul><li>Act as the lead investigator on employee concerns including devising investigation strategies, reviewing data and documents, conducting interviews and writing and communicating investigation summaries.</li><li>Provide coaching/supervision on investigations to less experienced members of ER team and HRBPs</li><li>Interact and engage with leadership in relation to investigations, including HR business partners and business managers.</li><li>Partner effectively with HR Business Partners, the legal team, Compliance, Quality Assurance, Security and others.</li><li>Collaborate with compliance and legal teams and HR leadership to address Ethics Points claims</li><li>Appropriately document, maintain, and handle sensitive and privileged and confidential information, including update and maintaining case and department data in relevant systems.</li><li>Advise HR Business Partners and other HR colleagues on employee relation processes & policies, and provide consultation on areas of overlap and/or impact</li><li>Act as a point of contact for ER.</li><li>Effectively build relationships with employees, managers, partners and leaders resulting in positive feedback.</li><li>Gather and analyze ER trends and data for HR leadership and SLT presentations.</li><li>Identify areas for improvement by leveraging analytics and data trends and/or discerning systemic issues revealed during the investigative process and recommend strategies and actions to address</li><li>Participate in projects led or impacting the ER team as needed</li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Experience analyzing ER data to identify trends and participating in developing ER strategy, preferred</li><li>Experience coaching more junior ER professionals, HRBPs and business leaders, preferred</li><li>Superb communication skills including effective listening, clear and concise writing and presentation</li><li>Proven interpersonal skills to negotiate, influence, and resolve issues at all levels in the organization and in collaboration with HRBPs and business leaders</li><li>Strong time management and prioritizing ability to balance multiple urgent assignments simultaneously</li><li>Consistently exhibits levels of discretion, integrity and confidentiality</li><li>Flexible and adaptable work demeanor to manage demands across multiple time zones</li><li>Respectful, diplomatic, and culturally sensitive in the face of difficult and sensitive situations and conversations</li><li>Ability to work both independently and as a team player in a cross-functional global team structure</li></ul><p><strong>To be considered for this role you must possess a Bachelor’s degree in a scientific discipline or HR related discipline (advanced degree such as MBA, or Master’s in Organization Development or Human Resources is preferred) with 7-9 years related work experience, including at least 4 years direct expereince as an investigator for Employee Relation matters</strong></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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Sunday-Thursday 3rd shift]]></title>
    <date><![CDATA[Sun, 21 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44084]]></requisitionid>
    <referencenumber><![CDATA[R44084]]></referencenumber>
    <apijobid><![CDATA[r44084]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44084/calibration-technician-sunday-thursday-3rd-shift/]]></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, working a Sunday-Thursday 10:00pm-8:30am shift. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</p><p><strong>Please note training will take place Monday-Friday 8:00am-4:30pm for 3-6 months based on experience level. 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>As a Calibration Technician, a typical day might include the following:</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></ul><h3>This role might be for you if you:</h3><ul><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>Seek to build and maintain positive working relationships with the business</li><li>Possess strong written and verbal communication skills</li><li>Maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p>To be considered for the Calibration Technician position you must be willing and able to work a Sunday-Thursday 10:00pm-8:30am schedule. 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><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>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 (hourly)</strong></strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Scientific Marketing - Ophthalmology]]></title>
    <date><![CDATA[Sun, 11 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44495]]></requisitionid>
    <referencenumber><![CDATA[R44495]]></referencenumber>
    <apijobid><![CDATA[r44495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44495/associate-director-scientific-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[<p>The Associate Director of Scientific Marketing, Ophthalmology is a member of Regeneron’s ophthalmology commercial marketing team, with accountability to help develop the strategic direction for scientific strategy and medical education activities. Activities include synthesis of insights from market research and congresses to impact brand narrative evolution, peer-to-peer educational programming, and related material development. The role will also be responsible for driving strategic advisory boards and consulting engagements as appropriate. As a key member of the Ophthalmology marketing team and will report to the Senior Director, Scientific Marketing.</p><p><strong>In this role, a typical day may include the following:</strong></p><ul><li>Working closely with Sr. Director, marketing team members and agency partners, develop and complete a scientific marketing plan which supports the long-term vision of the products</li><li>Collaborate with Scientific Marketing team to obtain and synthesize insights from market research, congresses, and KOL interactions, and apply findings to inform commercial strategy and execution.</li><li>Build and manage relationships with KOLs, HCPs, and professional partners, including KOL engagement planning.</li><li>Lead strategy for speaker bureau, including relevant and accurate content development</li><li>Contribute to the evolution of scientific narratives and the brand strategy</li><li>Develop scientific content for use across various media opportunities, in partnership with the marketing team</li><li>Contribute to overarching brand and tactical planning, liaising with agency partners to drive Scientific Marketing portion</li><li>Partner with Thought Leader Liaisons in driving speaker communications, optimizations, and engagements</li><li>Coordinate the Annual Advisory Board Plan (AABP), including the development and execution of US commercial advisory boards to support brand strategy.</li></ul><h3><strong>This role may be for you if you:</strong></h3><ul><li>You demonstrate a strong science background with experience in ophthalmology. Understanding and experience in Retina is a plus.</li><li>You bring creativity, strategic capabilities, and ability to work effectively in complex, rapidly changing environments</li><li>You have experience leading and developing medical education tactics, especially in biologics/high science products, and products with multiple indications (buy and bill experience an additional plus)</li><li>You can develop and implement educational programs targeting HCPs and related key customer groups, including activities such as advisory boards and congress-related marketing activities</li><li>You demonstrate strong interpersonal skills, including the ability to build alignment, inform, negotiate, and collaborate</li><li>You are willing to travel up to 25-30% (including weekend travel as needed)</li></ul><p>To be considered for this role, a minimum of 10 years professional experience in pharmaceutical marketing. Experience with pharmaceutical MLR processes is required. Lastly, we require you to be willing to work in a hybrid environment with a minimum of 4 days on-site at Sleepy Hollow, NY.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Jan 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Device Development Engineer (Project Leadership)]]></title>
    <date><![CDATA[Mon, 26 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44516]]></requisitionid>
    <referencenumber><![CDATA[R44516]]></referencenumber>
    <apijobid><![CDATA[r44516]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44516/sr-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>Regeneron is seeking a Sr. 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>A typical day for a Sr. Device Development Engineer might include:</p><ul><li>Leads multidisciplinary engineering project teams (Human Factors, V&V Engineering, Manufacturing Engineer, Quality Engineering) through the complete device design and development lifecycle of a combination product development within the Regeneron Pipeline.</li><li>Defines detailed product requirements and specifications with commercial, clinical, and other development/strategy collaborators.</li><li>Defines technical specifications and design requirements in collaboration with engineering teams (manufacturing, verification, packaging etc.)</li><li>Responsible for all user needs and requirements to be validated through design and development.</li><li>Develops, manages, and communicates development program plans, risks, timelines, and budgets to internal and external team members.</li><li>Integrate device development activities with Chemistry Manufacturing Controls (CMC) and Global development timing and goals.</li><li>Supports global internal manufacturing and external manufacturing teams around relevant design and process development information transfers.</li><li>Leads all aspects of product testing and quality assurance processes for the specific device development.</li><li>Ensures comprehensive and compliant Design History File (DHF) is developed and ensures to meet regulatory and quality requirements (21CFR Part 3 and 21 CFR 820.30).</li><li>Supports management in related clinical and commercial regulatory activities that is related to the device development (ie: IND/IMPD, BLA Submission, Clinical Pharmacy Manuals etc.)</li><li>Understands design inputs and outputs of multiple delivery systems and how it can impact end users.</li><li>Supports management and/or therapeutic area device project leads, in strategic product launch and go-to-market plans for the device development.</li></ul><p>This role might be for you if you:</p><ul><li>Understand relevant FDA regulations, particularly 21 CFR Part 3 and 21 CFR 820.30.</li><li>Have experience with design history file management (21 CFR 820.30).</li><li>Possess strong project management and interpersonal skills and strong analytical and problem-solving capabilities.</li><li>Can balance business objectives with technical constraints.</li><li>Can work effectively across multiple functional teams.</li><li>Enjoy working in a fast-paced, multifaceted research and development environment.</li><li>Are willing and able to travel for partner meetings, audits, and project coordination activities.</li></ul><p>To be considered for the Device Development Engineer you must have a B.S in Engineering and 5+ years or relevant experience; or equivalent combination of education & experience. Previous experience in product management/project management/ and/or project leadership related activities is required. Level is determined based on qualifications relevant to the role.</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>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 27 Jan 2026 09:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sourcing Manager]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44844]]></requisitionid>
    <referencenumber><![CDATA[R44844]]></referencenumber>
    <apijobid><![CDATA[r44844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44844/sourcing-manager/]]></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>Overview:</strong></p><p>Regeneron’s Global Procurement is a strategic team that powers the growth of a science-led company. Guided by our SVP’s clear vision to make procurement a competitive advantage, we are strengthening category leadership, expanding our Center of Excellence, and building an International Markets organization. This Japan-focused role is a core member shaping our next chapter—bridging global strategy with Japan’s unique market needs to deliver tangible impact.</p><p><strong>What You’ll Gain:</strong></p><p>End-to-end category accountability in Japan with real decision-making authority<br>A platform to infuse Japan’s market perspective into global strategies that drive business outcomes<br>Collaboration with the Center of Excellence and international country leads to design and implement best practices across markets<br>The pride and purpose of enabling life-changing scientific innovation through world-class procurement<br>A data-driven environment to sharpen skills in decision-making, negotiation, contracting, and supplier relationship management</p><p><br><strong>Role & Mission:</strong><br>Position Purpose</p><p>As the accountable lead for procurement activities in Japan, you will optimize supplier engagement and sourcing plans aligned to local commercial, regulatory, and site objectives—while ensuring Japan-specific requirements (regulatory, language, legal, commercial, medical, cultural) are addressed appropriately. This role reports to the Sr Manager, Global Procurement – Japan and partners closely with international country leads and category teams to enable global expansion and local priorities.</p><p>Key Responsibilities</p><p>Partner with stakeholders to translate global priorities into local execution in Japan<br>Deeply understand Japan’s supply base and ways of working to design optimal procurement strategies<br>Deploy global category strategies in-country to ensure consistent sourcing, contracting, and SRM<br>Feed Japan’s needs into global strategies to improve relevance and outcomes<br>Co-create standardized processes and best practices across the International Markets procurement team<br>Review local contracts and analyze spend data to identify trends and optimization opportunities<br>Anticipate business strategies, budgets, and annual spend needs to align procurement plans<br>Execute sourcing, negotiation, and contracting to deliver cost savings, cash flow improvements, and operational efficiencies<br>Apply biopharma procurement excellence to advance Regeneron’s procurement organization in line with corporate priorities<br>Use data to drive successful category decisions and outcomes<br>Coach procurement technical skills across the global team</p><p><br><strong>Qualifications:</strong><br>Basic Qualifications</p><p>Bachelor’s degree in a relevant field<br>5+ years of experience in Indirect Procurement<br>Proven success leading/supporting cross-functional teams across sourcing, negotiation, contracting, and SRM<br>Ability to build influential stakeholder and supplier relationships that drive results<br>Expertise in rates, unit costs, and cost structures to optimize negotiations<br>Habit of leveraging external data, market insights, and supplier engagement to deepen understanding of supply market dynamics<br>Integrity, focus, and clarity in ambiguous environments; ability to drive change and improvement<br>Experience with global supply market evaluation using market intelligence, risk, compliance, and financial assessment tools<br>Proficiency with Word, Excel, and PowerPoint for communication and analysis</p><p><br>Preferred Qualifications</p><p>Procurement experience in Pharma/Biopharma<br>Experience across Commercial, Corporate/Indirect, and R&D categories<br>Success supporting/leading global category teams, processes, and supplier management across diverse categories<br>Working knowledge of sourcing/contracting tools, ERPs, and eRFx systems (Oracle, Zycus, GEP, Ariba, others)</p><p><br><strong>Culture:</strong><br>Our Values</p><p>Regeneron is a company that leads with science. We relentlessly transform science into medicine for patients. Procurement is a crucial strategic enabler of that mission. Grounded in patient-first, integrity, and excellence, our “Doing Well by Doing Good” ethos aligns business success with social responsibility.</p><p><br><strong>Company Overview:</strong></p><p>Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. For more than 35 years, physician-scientists have led our unique R&D engine, producing numerous FDA-approved treatments and a robust pipeline—nearly all born in our own laboratories. Our medicines and pipeline address eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, pain, hematologic conditions, infectious diseases, and rare diseases. Headquartered in Tarrytown, NY, Regeneron has ~15,500 employees.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Minneapolis North, MN]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44975]]></requisitionid>
    <referencenumber><![CDATA[R44975]]></referencenumber>
    <apijobid><![CDATA[r44975]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44975/medical-specialist-i-dermatology-minneapolis-north-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>Geography: Minneapolis North, MN</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory. #derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Oncology)]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42019]]></requisitionid>
    <referencenumber><![CDATA[R42019]]></referencenumber>
    <apijobid><![CDATA[r42019]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42019/senior-manager-clinical-study-lead-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Clinical Study Lead</strong> (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is 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 out-sourced 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><em>This role is not eligible fully remote. This role is required to be onsite in one of our locations.</em></p><p><strong>A typical day in this role looks like: </strong> </p><ul><li>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</li><li>Provides operational input into protocol development</li><li>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</li><li>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</li><li>Ensures compliance with the clinical trial registry requirements</li><li>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors </li><li>Provides input into baseline budget development and management</li><li>Provides input into baseline timeline development and management</li><li>Leads risk assessment and identifies risk mitigation strategies at the study level</li><li>Leads the feasibility assessment to select relevant regions and countries for the study</li><li>Oversees/conducts site evaluation and selection</li><li>Leads investigator meeting preparation and execution</li><li>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</li><li>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</li><li>Monitors data entry and query resolution and acts on any deviations from agreed metrics</li><li>Ensures accurate budget management and scope changes for internal and external studies</li><li>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</li><li>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</li><li>Oversees the execution of the clinical study against planned timelines, deliverables and budget</li><li>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</li><li>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</li><li>Ensure clinical project audit and inspection readiness through the study lifecycle</li><li>Supports internal audit and external inspection activities and contributes to CAPAs as required</li><li>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</li><li>Contributes to clinical study report writing and review</li><li>Facilitates and contributes to study level lessons learned</li><li>Assigns tasks to Clinical Study Management staff and supports their deliverables</li><li>Recommends and participates in cross-functional and departmental process improvement initiatives</li><li>Responsible for identification of innovative approaches to clinical study execution including global considerations and continuous improvement of CTM SOPs</li><li>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</li><li>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</li><li>May require 25% travel</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Exceptional interpersonal & leadership skills</li><li>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</li><li>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</li><li>Advanced communication skills via verbal, written and presentation abilities</li><li>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</li><li>Ability to influence and negotiate across a wide range of stakeholders</li><li>Strong budget management experience</li><li>An awareness of relevant industry trends</li><li>Ability to build, lead and develop productive study teams and collaborations</li><li>Applies advanced negotiation and interpersonal skills to vendor management</li><li>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</li><li>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</li><li>Knowledge of ICH/GCP and regulatory guidelines/directives</li><li>Advanced project management skills, cross-functional team leadership and organizational skills</li><li>Line management experience</li></ul><p><strong>In order to be considered qualified, </strong>a minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Enterprise Integration]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44136]]></requisitionid>
    <referencenumber><![CDATA[R44136]]></referencenumber>
    <apijobid><![CDATA[r44136]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44136/associate-director-enterprise-integration/]]></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>The Associate Director of Enterprise Integration is a strategic and hands-on leader responsible for defining the integration vision, establishing governance, and delivering reliable, scalable, and secure integration capabilities across the enterprise. This role owns the integration platform and services as a product, sets design principles and leading practices, orchestrates work across application and corporate shared service teams, and ensures the portfolio delivers measurable business outcomes. They will inform technical and architecture strategy, stand up and qualify new technologies, and drive continuous improvement by reducing technical debt and standardizing work.</p><p>As an Associate Director, a typical day might include the following:</p><ul><li>Inform and define the technical and architecture strategy for enterprise integration (roadmaps, tools/technology selection, platforms, patterns, standards).</li><li>Establish design principles and leading practices for APIs, architecture, data movement, orchestration, and security.</li><li>Support standing up new technology and qualifying through proofs of concept, pilots, and vendor evaluations.</li><li>Lead decisions on “which bus to get on” (e.g., ESB, event bus, streaming backbone) aligned to use cases and scalability goals.</li><li>Create and maintain an Integration “Pattern” Decision Framework to guide synchronous vs. asynchronous, pub/sub vs. request/response, batch vs. streaming, ETL vs. ELT, and choreography vs. orchestration choices.</li><li>Establish and run governance processes including intake, prioritization & work management; create and maintain Standard Work (SOPs, playbooks, runbooks, checklists) for design, build, test, deploy, and support.</li><li>Maintain an authoritative Integration Catalog of APIs, events, integrations, schemas, SLAs, and ownership.</li><li>Serve as Product Owner for the Integration Platform and shared integration services, defining vision, roadmap, backlog, and success metrics.</li><li>Orchestrate work across application teams, corporate functions (security, compliance, finance), and programs to ensure alignment and remove blockers.</li><li>Provide project management oversight across the integration portfolio: scope, timeline, budget, dependencies, risk management, and status reporting.</li><li>Drive integration quality through design reviews, pattern adherence, testing standards, and observability.</li><li>Identify, prioritize, and remediate integration technical debt (legacy patterns, brittle point-to-point, insufficient observability, poor documentation).</li><li>Implement practices for reusability, versioning, deprecation, and lifecycle management of integrations.</li><li>Own integration financials: annual budgeting, forecasting, vendor/software costs, cloud consumption, and chargeback models.</li><li>Measure and communicate ROI, TCO, and value realization of integration investments.</li></ul><p>This role may be for you if you have:</p><ul><li>Proven experience with integration platforms (iPaaS, ESB, API gateway, event streaming), such as IBM MQ, MuleSoft, Boomi, Azure Integration Services, Kafka/Confluent, AWS/GCP integration suites, or similar.</li><li>Strong grasp of integration patterns (EDA, pub/sub, CQRS, SAGA, orchestration/choreography), data movement (ETL/ELT), and API lifecycle management; knowledge of integration platforms such as Oracle Integration Cloud (OIC), middleware, and APIs.</li><li>Familiarity with enterprise architecture frameworks (e.g., TOGAF), agile at scale (e.g., SAFe), and ITIL service management practices.</li><li>Solid understanding of security, compliance, privacy, identity, and data governance as they apply to integrations.</li><li>Demonstrated success in establishing governance, standard work, and cross-functional orchestration with measurable outcomes.</li><li>Familiarity of regulatory guidelines, including GxP compliance, Sox, and security.</li><li>Expertise in Oracle SQL, PL/SQL, and reporting tools like Oracle BI Publisher and OTBI.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Senior Manager: 8+ years in enterprise integration, middleware, or API/platform architecture; 4+ years in leadership roles.</li><li>Associate Director: 10+ years in enterprise integration, middleware, or API/platform architecture; 5+ years in leadership roles.</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>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Brentwood, NY]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45011]]></requisitionid>
    <referencenumber><![CDATA[R45011]]></referencenumber>
    <apijobid><![CDATA[r45011]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45011/medical-specialist-i-dermatology-brentwood-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Brentwood]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Brentwood, NY</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 08:56:53 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director,  Medical Affairs, Neurology]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45222]]></requisitionid>
    <referencenumber><![CDATA[R45222]]></referencenumber>
    <apijobid><![CDATA[r45222]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45222/executive-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>The Executive Medical Director, Medical Affairs, Neurology will fulfill an important strategic leadership role reporting into the SVP of Medical Affairs. This role has high visibility in the organization, participating with senior management in developing strategic objectives and implementing functional Medical Affairs plans for Neurology assets focused on Mysathenia Gravis with the benefit of the patient at the forefront. We are planning for future indications in Neurology in the near future.</p><p>A day in the life of an Executive Medical Director may include the following:</p><ul><li>Ensures that strategic long term and annual conceptualization and execution of US and Global Medical Affairs plans for late stage Neurology products/compounds are appropriately aligned with corporate strategies.</li><li>Development and execution of US and globally focused medical strategy and tactics, including internal/ external disease area/ product training, annual medical planning, scientific communications, and collaborations with experts.</li><li>Application of therapeutic/disease area expertise and addressing current and future medical needs in clinical practice to inform medically appropriate use of investigational medicines.</li><li>Oversight and hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications.</li><li>Development and cultivation of long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external stakeholders representing Regeneron.</li><li>Provides guidance and fosters professional development and growth of direct reports</li><li>Demonstrates excellent people management skills, as well as collaborative efforts with relevant stakeholders internally and externally</li></ul><p>This job may be for you if you have the following:</p><ul><li>Advanced degree (MD, PhD or PharmD), MD preferred</li><li>Specialized clinical training in Neurology or Neurology experience through industry</li><li>14+ years total experience post (medical) degree, with at least ten years progressive experience in Pharmaceutical or Biotech Industry working in Medical Affairs and/or Clinical Research & Development or related fields.</li><li>Ability to collaborate well with commercial and market access teams in the setting of a commercial launch.</li><li>Possesses clinical knowledge in a range of diseases within Neurology (Myasthenia Gravis preferred).</li><li>Industry experience in planning, executing and reporting clinical trials with post-marketing experience required.</li><li>Prior experience working in a matrix organization as well as cross-functional collaboration with commercial/marketing departments strongly desired.</li><li>Experience working with field-based colleagues/MSLs required.</li><li>Strong leadership and management skills #MDJOBS, #MDJOBSMA, #GDMAJobs</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>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) – Dermatology Fukushima Area]]></title>
    <date><![CDATA[Fri, 06 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45738]]></requisitionid>
    <referencenumber><![CDATA[R45738]]></referencenumber>
    <apijobid><![CDATA[r45738]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45738/medical-representative-mr-dermatology-fukushima-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Assigned Area: </strong></p><p>You will primarily work in the Fukushima area. </p><p>Your residence is expected to be in Fukushima.(Miyagi also available for consultation)</p><p><strong>Job Overview: </strong></p><p>While embodying Regeneron’s philosophy of "putting patients first," you will play a key role in the Immunology Department's dermatology division by managing Dupixent and achieving sales targets. </p><p>Utilizing excellent business acumen and strategic thinking, you will aim to achieve and exceed corporate goals by building trust-based relationships with customers and offering valuable solutions. </p><p><strong>Main Responsibilities: </strong></p><p>- Budget and expense management to achieve brand sales targets </p><p>- Developing and implementing annual business plans using market insights </p><p>- Building strategic sales plans based on key data </p><p>- Performing various administrative tasks (e.g., expense reporting, marketing reports) </p><p>- Compliance with regulations and legal requirements </p><p>- Participation in area meetings and nationwide conferences </p><p>- Completion of training programs and skill development </p><p>- Travel as needed (including nights and weekends) </p><p>- Conducting business safely while driving </p><p><strong>Required Skills and Experience: </strong></p><p>- Sales experience targeting university hospitals </p><p>- Specialized knowledge in dermatology and sales experience with biologics </p><p>- Excellent customer engagement and communication skills </p><p>- Strategic thinking and ability to work independently </p><p>- Proficiency in IT and digital tools </p><p>- Experience in joint promotions with alliance companies </p><p><strong>Preferred Qualifications: </strong></p><p>- Clinical knowledge of competitive brands or therapeutic areas </p><p>- Network with key opinion leaders in dermatology </p><p>- English proficiency is a plus </p><p><strong>Eligibility: </strong></p><p>- Bachelor’s degree (or equivalent qualification) </p><p>- Over 5 years of sales experience in the pharmaceutical industry </p><p>- MR certification and a valid driver’s license </p><p><strong>Advance Your Career to the Next Level: </strong></p><p>Regeneron provides an environment where every employee can maximize their potential. This is a rewarding position that allows you to leverage your expertise in the dermatology field to deliver significant value to patients and healthcare professionals. This challenge offers an opportunity to elevate your career to new heights.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 02:26:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Lab Study Manager]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45212]]></requisitionid>
    <referencenumber><![CDATA[R45212]]></referencenumber>
    <apijobid><![CDATA[r45212]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45212/senior-manager-clinical-lab-study-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>The Senior Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Senior Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology (IO). 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>As a CLSM Senior Manager, a typical day may include the following:</strong></p><p><strong>Clinical Trial Study Team Support</strong></p><ul><li><p>Participates in cross-functional study teams and sub-teams across clinical and research departments</p></li><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>Support cross functional internal and external collaborators to manage and support the generation of high-quality laboratory data.</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>Serves as CLSM subject matter expert contact for assigned therapeutic areas including IO.</p></li><li><p>Allocates and prioritizes FSP CLSM and Sr. PMA resources within the assigned therapeutic program and studies.</p></li><li><p>Manages FSP CLSM team for technical and operational support on their assigned therapeutic program and studies.</p></li></ul><p><strong>Operational Support of Sample Analysis (Including Exploratory Analysis)</strong></p><ul><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>Forecasts sample related operational costs and reviews invoices to ensure we are aligned with budget plans</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>Prepares RFPs, reviews and assess bids and SOWs for items related to samples and testing</p></li><li><p>Provides guidance and trainings to vendors, collaborators and clinical sites on sample collection, processing, shipping, and storage</p></li></ul><p><strong>Data Acquisition and Management </strong></p><ul><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>Human Sample Management Flow and Compliance</strong></p><ul><li><p>Provides guidance to clinical teams and clinical sites regarding collection and storage of samples acquired during clinical trials or other human sample acquisition projects</p></li><li><p>Works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable ICF</p></li><li><p>Collaborates with internal Human Sample Management team to ensure all samples transferred to internal research groups are documented, tracked, used, and destroyed</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, and direct projects and work cross-functionally to manage expectations with excellent communication and collaborative skills and work well in a team-based environment. The CLSM Senior Manager will be responsible for day-to-day oversight of multiple CLSMs, including responsibility for coaching, mentoring and performance management ensuring applicable key trial level milestones are achieved on schedule.</p></li><li><p>You demonstrate strong leadership skills and possess high level of emotional intelligence and effectively work collaboratively with colleagues, vendors and internally at Regeneron to ensure program success.</p></li></ul><p><strong>To be considered for this role, you must have</strong> a Bachelors, Minimum of 8 years pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. Minimum of 5 years’ experience with Clinical Trials, focus on clinical sample collection. Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested. We need a strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required. We are seeking clinical study knowledge, demonstrated by knowledge in science and technology. Demonstrated experience in stake holder management, leading internal and external meetings and solutioning skills.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 14:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Sun, 22 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45490]]></requisitionid>
    <referencenumber><![CDATA[R45490]]></referencenumber>
    <apijobid><![CDATA[r45490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45490/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>Regeneron is seeking a Manager, of Advertising and Promotion to join our Regulatory Affairs team!!</p><p><strong>In this role, a typical day might include:</strong></p><p>The 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). 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><strong>This role might be for you if you can/Have</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>To be considered for this opportunity, you must have the following:</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><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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Plant Utilities Technician, Wednesday-Saturday 1st shift]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45325]]></requisitionid>
    <referencenumber><![CDATA[R45325]]></referencenumber>
    <apijobid><![CDATA[r45325]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45325/plant-utilities-technician-wednesday-saturday-1st-shift/]]></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 fill a Plant Utilities Technician position with a Wednesday-Saturday 6:00am-4:30pm schedule. Our Plant Utilities Technicians are responsible for start-up, normal operation, monitoring, maintaining and shutdown of Plant Utility systems and equipment within Plant Utility mechanical rooms that support overall facility buildings.</p><p><strong>Please note training will be Monday-Friday 7:00am-3:30pm for the first few months. Working hours thereafter will be Wednesday-Saturday 6:00am-4:30pm. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Plant Utilities Technician, a typical day might include the following:</p><ul><li>Maintaining high pressure steam and hot water boilers, controls and associated equipment</li><li>Maintaining boiler and cooling tower chemical treatment program</li><li>Maintaining all other Plant Utility equipment such as boiler pretreatment water, condensate return, natural gas, domestic potable water, tepid water, wastewater</li><li>Monitoring controls of plant systems using Building Automation System (BAS) or Programmable Logic Controls (PLC)</li><li>Reviewing, monitoring, responding and reacting to alarm notifications from the Building Automation Systems</li><li>Performing Plant Utility monthly Preventative Maintenance</li><li>Planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Scheduling, assigning, completing and reviewing incursions specific to Plant Utility activities</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Coordinating the execution of small departmental Plant Utility projects</li><li>Maintaining documents and records on all plant equipment and systems</li><li>Collaborating with other departments, contractors and subject areas on scheduling repairs and maintenance of plant utility systems</li><li>Maintaining and ordering adequate equipment, spare parts and supplies for Plant Utility inventory</li><li>Participating in on-call rotation</li></ul><p>This role might be for you if you:</p><ul><li>Have experience with or knowledge of high-pressure boilers and waste neutralization</li><li>Are not afraid to work with chemicals and steam</li><li>Follow current good manufacturing practices (cGMPs) and good business practices.</li><li>Demonstrate basic problem solving skills</li><li>Able to build and maintain positive working relationships with the business</li><li>Can learn and follow routine procedures independently as well as part of a team</li><li>Find working in an environment with changing priorities exciting</li><li>Can lift, push, and/or pull at least 50 lbs</li><li>Are able to prioritize and shift focus when needed</li></ul><p>To be considered for the Plant Utilities Technician you must be willing and able to work Wednesday-Saturday 6:00am-4:30pm. 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>Plant Utilities Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Plant Utilities Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li></ul><p>Prior experience in the maintenance and operation of large scale utilities plant preferred.</p><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 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 (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Feb 2026 14:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Pharmacovigilance ICSR Intake - AI Enablement]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45231]]></requisitionid>
    <referencenumber><![CDATA[R45231]]></referencenumber>
    <apijobid><![CDATA[r45231]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45231/senior-manager-pharmacovigilance-icsr-intake-ai-enablement/]]></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>Regeneron is seeking a Senior Manager, Pharmacovigilance ICSR Intake - AI Enablement to join our Patient Safety Team!</p><p><strong>In this role, a typical day might include:</strong></p><p>This position is responsible for providing strategic oversight and operational leadership for global Individual Case Safety Report (ICSR) intake activities. This role ensures the timely, accurate, and compliant receipt, triage, and delivery of safety data in accordance with ICH‑GCP/GVP guidelines, global regulatory requirements, and Regeneron procedures.</p><p>This position oversees all sources of safety data—including spontaneous reports, clinical trials, literature, digital channels, medical information call centers, partner organizations, and AI‑enabled intake tools—while ensuring high standards of source data quality, data integrity, and regulatory compliance. The role partners cross‑functionally to streamline intake operations and leads modernization initiatives that leverage technology, automation, and process innovation to enhance efficiency, quality, and scalability.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Operational Leadership</em></p><ul><li><p>Oversee global ICSR intake operations to ensure timely case receipt, acknowledgment, triage, and handoff to downstream safety processing teams.</p></li><li><p>Serve as the subject matter expert (SME) for ICSR intake processes, technologies, and regulatory expectations including presentations to senior leadership and representing the team during audits and inspections.</p></li><li><p> Manage intake‑related vendors, including performance oversight, SLA/KPI management, and issue escalation.</p></li></ul><p><em>Technology, Innovation & Automation</em></p><ul><li><p>Lead the evaluation, implementation, and optimization of AI‑enabled intake tools, automated data ingestion, natural language processing (NLP) capabilities, workflow automation, and system upgrades.</p></li><li><p>Partner with Safety Systems and IT to enhance the PV Intake Tool, workflow engines, and safety database interfaces.</p></li><li><p>Drive modernization projects aimed at reducing manual workload and improving throughput, data quality, and compliance.</p></li></ul><p><em>Source Data Quality & Compliance</em></p><ul><li><p>Ensure all intake activities meet global regulatory requirements, SOPs, and inspection‑ready standards.</p></li><li><p>Monitor intake volume and quality, ensuring completeness, accuracy, and consistency of source data across channels.</p></li><li><p>Investigate quality or compliance issues, identify root causes, and lead the development and implementation of corrective and preventive actions (CAPAs).</p></li></ul><p><em>Cross‑Functional Collaboration</em></p><ul><li><p>Collaborate with internal partners (e.g., Medical Affairs, Clinical Operations, Commercial Quality, Digital/Social Monitoring teams) and external collaborators to support intake processes and safety data flow.</p></li><li><p>Ensure effective and compliant ICSR transmission between intake systems, call centers, EDC systems, partner organizations, and the safety database.</p></li></ul><p><em>Process Excellence & Continuous Improvement</em></p><ul><li><p>Identify operational and system improvement opportunities and lead cross‑functional initiatives to optimize intake workflows.</p></li><li><p>Contribute to or lead the creation and revision of SOPs, work instructions, training materials, and job aids.</p></li><li><p>Provide training, mentorship, and guidance to staff on intake processes, technologies, and regulatory requirements.</p></li></ul><p><em>Leadership</em></p><ul><li><p>May manage and develop assigned personnel, ensuring role clarity, performance feedback, and career development.</p></li><li><p>Model professionalism, collaboration, adaptability, and a commitment to continuous learning and operational excellence.</p></li><li><p>Perform other related duties as assigned or requested by Manager for business needs.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree preferred in life sciences, clinical research, or a healthcare discipline.</p></li><li><p>Minimum of 10 years of relevant industry experience with a Bachelor’s degree, or 7 years with a Master’s degree, in pharmacovigilance, safety operations, or safety reporting.</p></li><li><p>Experience with ICSR intake systems, automated workflows, digital channels, and vendor oversight.</p></li><li><p>Proficiency with Microsoft Office applications and safety database tools.</p></li><li><p>Willingness and ability to travel domestically as required.</p></li><li><p>Strong understanding of global pharmacovigilance regulations, ICSR processes, and the adverse event lifecycle.</p></li><li><p>Advanced expertise in intake‑related technology, automation, artificial intelligence (AI)/machine learning (ML) applications, and safety systems (e.g., Argus).</p></li><li><p>Ability to independently identify, analyze, and solve complex operational and data‑related issues.</p></li><li><p>Excellent written and verbal communication skills; able to convey complex concepts clearly.</p></li><li><p>Strong organizational, prioritization, and project‑management capabilities.</p></li><li><p>Demonstrated ability to work collaboratively across functions and with external partners.</p></li><li><p>Strong attention to detail and commitment to data quality and compliance.</p></li><li><p>High level of professionalism, integrity, and customer‑service orientation.</p></li></ul><p> #GDPSJobs</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ICSR Knowledge & Process Optimization]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45882]]></requisitionid>
    <referencenumber><![CDATA[R45882]]></referencenumber>
    <apijobid><![CDATA[r45882]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45882/director-icsr-knowledge-process-optimization/]]></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>Regeneron is seeking a Director, ICSR Knowledge & Process Optimization to join our organization.</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director of ICSR Knowledge & Process Optimization is accountable for developing, maintaining, and continuously improving global procedures, standards, and tools that enable high-quality, compliant, and efficient individual case safety report (ICSR) processing and adverse event reporting across both developmental and marketed products. This role ensures end-to-end ICSR process robustness—from intake through expedited submissions and periodic reporting—by driving harmonized procedures, risk-based quality controls, and technology-enabled automation. The Director partners closely with GPS Standards and Training, Signal Management, Safety Sciences, Clinical Development, Quality/QA, Regulatory, Medical Information, IT, and Commercial to ensure timely compliance with global regulations while advancing operational excellence.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Ability to further develop and maintain processes for high quality and compliant</p></li><li><p>ICSR case processing from all sources for reporting to all applicable destinations. This includes owning the global ICSR process framework: standards, SOPs, Work Instructions (WIs),</p></li><li><p>Job aides, data entry conventions (DECs), templates, decision trees, and training curricula for all case types for the various resources performing case evaluation, medical assessment, and submissions.</p></li><li><p>Ensure procedural alignment to global regulations and guidance.</p></li><li><p>Map end-to-end processes (intake → triage → data entry → medical review → case finalization → submissions → follow-up → reconciliation); identify waste, bottlenecks, and process failures. This includes partnering with IT/Safety Systems to evaluate, pilot, and scale technologies and automation.</p></li><li><p>Define and review key performance indicators to ensure training compliance and effectiveness (e.g. first time right (FTR); rework/cycle time; quality event/CAPA closure timelines, etc.)</p></li><li><p>Curate and maintain the ICSR Knowledge Base (product/study-specific conventions, seriousness criteria, causality heuristics, MedDRA coding conventions, follow-up rules, local regulatory nuances, partner agreements).</p></li><li><p>Standardize and deploy role-based training and certification for internal teams and vendors; measure learning effectiveness and error reduction.</p></li><li><p>Partner with Vendor Relationship Management/QA/other stakeholders to ensure vendor procedures align to sponsor standards; define hand-offs, SLAs, and reconciliation controls (e.g., MI/Call Center, literature vendors, third party vendors).</p></li><li><p>Oversee readiness for internal audits and Health Authority inspections; lead remediation plans and CAPAs related to ICSR processes.</p></li><li><p>Performs other related duties as assigned or requested per business needs.</p></li><li><p>Able to independently identify, analyze, and resolve moderate to complex issues and trends. </p></li><li><p>Strong knowledge of global pharmacovigilance regulations, systems, and processes and ability to translate those into efficient and auditable procedures. </p></li><li><p>Previous people management experience with the ability to mentor and develop direct reports. </p></li><li><p>Excellent written and verbal communication skills. Able to express complex ideas. </p></li><li><p>Able to align diverse stakeholders and influence across teams, departments and geographies. </p></li><li><p>Able to identify and document regulatory non-compliance and any related issues. </p></li><li><p>Plans and executes change management; measures adoption and outcomes. </p></li><li><p>Uses metrics to prioritize and verify improvements; comfortable with data and dashboards. </p></li><li><p>Excellent organizational and interpersonal skills. </p></li><li><p>Attention to detail; able to identify and resolve discrepancies on compliance reports.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor's Degree in one of the life sciences or clinical research and/or a licensed healthcare professional required.</p></li><li><p>Minimum of 12 years of experience in safety and safety reporting.</p></li><li><p>Equivalent combination of relevant education and experience.</p></li><li><p>Computer literacy and experience working with Microsoft Office (Word, Excel, PowerPoint) required</p></li><li><p>Excellent knowledge of Argus and its applications.</p></li><li><p>Excellent verbal and written communication skills required.</p></li><li><p>Excellent interpersonal and organizational skills required.</p></li><li><p>Ability to work independently, prioritize effectively and work in a matrix team environment required.</p></li><li><p>Ability and willingness to travel domestically as required.</p></li></ul><p>#GDRAJobs</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Inspection Management (GCP)]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R38901]]></requisitionid>
    <referencenumber><![CDATA[R38901]]></referencenumber>
    <apijobid><![CDATA[r38901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r38901/associate-director-inspection-management-gcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management of GCP, GVP and GLP inspections. The GDQIM IML will engage with key stakeholders, build strategic partnerships working and liaising with Clinical Study teams, relevant functions and other GDQ functions to support teams with inspection preparation activities on all Regeneron-sponsored clinical trials.</p><p><strong>In this role, a typical day might include the following:</strong></p><p>Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.<br>• Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.<br>• Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.<br>• Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.<br>• Identifying and discussing with the Clinical Study Teams potential issues and/or gaps, in advance of an impending inspection, that may require strategies to mitigate risk and/or provide additional clarification to an inspector.<br>• Ensuring the preparation, management and conduct of inspection preparation sessions which include mock inspections, trainings, and clinical site preparation visits working with GDQA team to identify and mitigate risks to clinical programs.<br>• Serving as the back room lead/co-lead or front room co-lead, responsible for explaining, managing,and ensuring the execution of all activities, including managing the tracking of requests and inquiries, and coordinating requests for responses from relevant personnel during any regulatory inspection conducted worldwide.<br>• Responsible for managing the preparation and provision of timely inspection updates and daily/end of inspection summaries to GD Executive and Senior Management, in addition to any other key relevant internal and external stakeholders.<br>• Responsible for managing inspection response development, and Corrective Actions/Preventive Actions (CAPA) follow-up activities alongside other GDQIM colleagues, cross-functional stakeholders, and process owners.<br>• Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.</p><h3><strong>This role may be for you if have:</strong></h3><p>• Advanced knowledge, understanding and application of GCP, and/or GVP <br>guidelines including the management of significant/complex quality issues <br>and compliance activities.<br>• Extensive experience with participating in, and supporting, Regulatory <br>Agency Inspections of Investigator Sites, Sponsors and Clinical Research <br>Organizations (CROs) in a GxP environment, including inspection <br>preparation, facilitation, and follow-up.<br>• Effective management of interpersonal relationships, stakeholder <br>engagement, and collaborations.<br>• Demonstrated ability to interface and collaborate effectively with other <br>Managers and Directors within, and external to, the organization.<br>• Extensive experience in providing training and presenting information on <br>key quality and regulatory compliance information.</p><p><strong>To be considered for this opportunity we are looking for:</strong></p><p>Bachelor's degree with a minimum of 10 years of relevant <br>healthcare/pharmaceutical industry experience.<br>• Experience working in either a quality/compliance role (e.g., Quality <br>Management, Quality Assurance etc.), or in a Clinical Development role <br>with expertise and/or transferable skills related to Good Clinical Practice <br>(GCP), and/or Good Pharmacovigilance Practice (GVP).<br>• Experience in training, supervising, line management, mentoring and <br>development of staff, and leading a small team</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Regeneron Genetics Medicines]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46057]]></requisitionid>
    <referencenumber><![CDATA[R46057]]></referencenumber>
    <apijobid><![CDATA[r46057]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46057/manager-clinical-scientist-regeneron-genetics-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>We are seeking a Manager, Clinical Scientist to join our Genetics Medicines team. The Manager, Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Manager works in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to the Sr Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>As a Manager within Clinical Sciences, a typical day may include the following:</strong></p><ul><li>Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings</li><li>May contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments</li><li>Develops/maintains basic 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 limited knowledge of disease and drug landscape</li><li>Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets</li><li>May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborate with others for scientific and foundational guidance</li><li>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</li><li>May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)</li><li>Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</li><li>Supports identification of data trends and potential inconsistencies in data across assigned studies and raises</li><li>Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>Demonstrated basic knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills</li><li>Demonstrate some ability to influence within study team</li><li>Independently resolves most issues and complex matters, requiring advanced analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues</li><li>Strong management, interpersonal and problem-solving skills</li><li>Proven track record in clinical trial process improvements</li><li>Considerable organizational awareness, including significant experience working cross-functionally</li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related area. Additionally, ≥ 6 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in immune/inflammatory related clinical trials. Basic knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 22:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs (Gastroenterology / Allergy )]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41443]]></requisitionid>
    <referencenumber><![CDATA[R41443]]></referencenumber>
    <apijobid><![CDATA[r41443]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41443/medical-director-medical-affairs-gastroenterology-allergy/]]></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 seeks a dedicated Medical Director, Medical Affairs, who prioritizes patient care above all else. The successful candidate will drive the development and execution of medical strategies and activities related to Regeneron's strategic assets in the Gastroenterology, Rhinology & Allergy/Immunology disease area, ensuring integrity and scientific accuracy. This role requires deep expertise in Eosinophilic Esophagitis (EoE) and related diseases, and clinical trial execution.</p><div><div><div><div><p><strong>A typical day in the life of a Medical Director, Medical Affairs may include the following responsibilities: </strong></p><p>• Develops and oversees implementation of US and ex-US focused medical strategy and tactics, including scientific communications and publications, annual medical planning, field communications, and collaborations with experts.<br>• Supports the design, conduct, oversight, analysis, and reporting of Medical Affairs post-approval interventional and non-interventional respiratory clinical trials.</p><p>• Attends clinical study team meetings, data oversight review sessions, and works closely with CRO medical monitors in support of medical affairs clinical trials.</p><p>• Oversees and provides hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications.</p><p>• Collaborates effectively within a multifunctional, matrix organization which includes field medical teams, medical operations, education, information, HEOR, publication management, and statistics.<br>• Develops and cultivates long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external stakeholders.</p><p>• Supports commercial activities such as promotional materials review, speaker training, colleague training, etc.</p><p><strong>This role may be for you if you have the following:</strong></p><p>• Physician (MD/MBBS or equivalent medical degree) with specialized training AND experience in gastroenterology or allergy/immunology, specifically EoE</p><p>• 0-4 years of industry experience in GI/Immunology Medical Affairs and/or Clinical Development (academic research experience will be considered)</p><p>• Demonstrated experience in clinical trial execution</p><p>• Experience working in an alliance setting is strongly preferred</p><p>• Lead complex business and technical discussions internally and externally and explain scientific/medical concepts to all levels<br>• Cultivate relationships and establish trust with internal and external Medical Experts in pulmonology.</p><p>• Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management.</p><p>• You thrive in a very dynamic environment in a therapeutic area with other competing treatment options.</p><p>#MDJobs, #MDJOBSMA, #GDMAJobs</p></div></div></div></div><ul></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>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process & Procedure Portfolio Specialist]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45106]]></requisitionid>
    <referencenumber><![CDATA[R45106]]></referencenumber>
    <apijobid><![CDATA[r45106]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45106/process-procedure-portfolio-specialist/]]></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>Join our dynamic team in Warren as a P&P Specialist, where you’ll play a pivotal role in supporting Global Development Process & Procedure’s portfolio management activities. This position offers the opportunity to work independently within a complex global environment, contributing to the controlled document development lifecycle. With minimal guidance, you’ll leverage your expertise to enhance operational efficiency and make a meaningful impact on our team’s success.</p><h3><strong>A Typical Day:</strong></h3><p>As a P&P Specialist, your daily responsibilities will include:</p><ul><li>Developing and maintaining tools to monitor and track procedural document portfolios.</li><li>Support the identification and compilation of metrics.</li><li>Leading portfolio reviews with P&P Leads, including KPI assessments and risk escalations.</li><li>Creating and executing standard reports, dashboards, and metrics to meet organizational needs.</li><li>Analyzing portfolio data to identify trends, risks, and improvement opportunities.</li><li>Supporting compliance activities related to audits, inspections, and process deviations.</li><li>Monitoring project plans for compliance and tracking their status.</li><li>Streamlining team files, communication templates, and repositories for operational efficiency.</li><li>Coordinating logistics for internal and external meetings, ensuring follow-up on actions.</li><li>Organizing and maintaining onboarding materials for new team members.</li></ul><h3><strong>This Role May Be For You If:</strong></h3><ul><li>You excel in analyzing data trends, developing metrics, and leveraging visualization tools to drive decision-making.</li><li>You’re proficient in project management principles and thrive in managing competing priorities.</li><li>You enjoy collaborating across teams and communicating effectively at all organizational levels.</li><li>You have a detail-oriented mindset, ensuring accuracy and adherence to standards.</li><li>You’re self-motivated and capable of working independently with minimal supervision.</li><li>You’re experienced in using AI tools and Electronic Data Management Systems (EDMS).</li><li>You’re passionate about contributing to a regulated, global environment, preferably in biopharma.</li></ul><h3><strong>To Be Considered:</strong></h3><p>Candidates must hold a Bachelor’s Degree with at least 2 years of relevant experience. Strong expertise in Microsoft Office (Excel, PowerPoint), data analysis, and visualization tools is essential. Experience in biopharma or using EDMS is preferred.</p><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 (hourly)</strong></strong></p>$34.47 - $56.20]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 16:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Biostatistics - Patient Reported Outcomes (PRO)]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46050]]></requisitionid>
    <referencenumber><![CDATA[R46050]]></referencenumber>
    <apijobid><![CDATA[r46050]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46050/manager-biostatistics-patient-reported-outcomes-pro/]]></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 seeking a Manager, Biostatistics - Patient Reported Outcomes (PRO) to join our team!</p><p>The Manager of Biostatistics for Patient Reported Outcomes (PRO) analysis will support multiple programs across therapeutic areas and cultivate strong partnerships to enable effective cross-functional collaboration with other product team members from internal groups including BDM, Medical Affairs/HEOR, Clinical Development, Regulatory Affairs and other functions as needed. In addition, the Manager of Biostatistics for PRO analysis will support collaborations with external partners (e.g. CROs, industry consortiums, key opinion leaders). He/She will work with the Director of Biostatistics for PRO to drive and establish best practices with regards to PRO analyses.</p><p><strong>In this role, a typical day might include:</strong> ​</p><ul><li><p>Support the analysis of PRO data ensuring methodological rigor, and regulatory adherence. </p></li><li><p>Create and refine statistical analysis plans, conduct complex statistical analyses and convey findings to internal and external stakeholders. </p></li><li><p>Apply fit for purpose statistical methods tailored to specific study objectives, ensuring robust data interpretation and insight generation. </p></li><li><p>Develop working knowledge of Regeneron asset(s) and support efforts to apply appropriate tools within therapeutic areas. </p></li><li><p>Strong understanding of data sources and leverage hands on data review to guide the selection of appropriate techniques and methods. </p></li><li><p>Authoring of technical documents including statistical analyses plans, programming specifications and TFL mock shells. </p></li><li><p>Support statistical efforts for assigned projects, manage timelines, resources, and coordinate across departments and external stakeholders</p></li><li><p>Stay informed on industry trends, incorporate emerging biostatistical methods to enhance analysis and participate in methodological research for the development of analytical techniques.</p></li><li><p>Assist preparation for biostatistical support on PRO analysis during regulatory interactions, and provide statistical efforts to address queries to ensure alignment with regulatory standards for organizational decision-making processes.</p></li><li><p>Stay informed with guidance documents from regulators to industry on use of PROs for regulatory decision making.</p></li></ul><p><strong>This role might be for you if you can/have:</strong> ​</p><ul><li><p>Strong interest and motivation in exploring PRO data for post-hoc analysis and innovative idea investigations</p></li><li><p>Experience with designing clinical trials especially observational types of studies</p></li><li><p>Exposure to study endpoints and analysis techniques across multiple therapeutic areas</p></li><li><p>Strong communication skills to interpret, explain, and discuss results of complex statistical concepts and analyses to both technical and non-technical audiences.</p></li><li><p>Desire to present and share results with internal and external stakeholders. </p></li><li><p>Experience with providing scientific/statistical input into study design, formulating novel problem-solving methods and independently developing the statistical analysis plan to implement those solutions.</p></li><li><p>Experience of authoring Statistical Analysis Plans (SAP), PRO SAP and Protocols </p></li><li><p>Experience with innovative ways to generate tables, listings, and figures for external communication use in publications/presentations and for internal purposes.</p></li><li><p>Ability to translate and apply relevant innovative statistical methodology to everyday work.</p></li><li><p>Experience of educating and disseminating knowledge throughout the organization for areas within the expertise of medical affairs.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD / DrPH in statistics/biostatistics or related disciplines with >2 years experience in the pharmaceutical/biotech industry or MS degree in statistics/biostatistics with >7 years’ experience in the pharmaceutical industry or academic organization as a statistician. </p></li><li><p>Knowledge of current statistical methods, at least 2 years using SAS/R/Python to solve statistical problems</p></li><li><p>Strong knowledge in advanced statistical methodology to support different endpoints common to PROs. </p></li><li><p>Strong knowledge with analysis using the clinical database for scientific meetings, publications, and internal decision-making (generally based on previously conducted randomized clinical trials). </p></li><li><p>Strong knowledge in statistical methods to support Health Economics and Outcomes Research including patient reported outcomes (including development/validation), HTA/reimbursement/value dossiers, and real-world studies.</p></li><li><p>Experience in statistical methods to support new studies including randomized studies, observational (non-randomized) studies, registries, non-interventional studies, cluster randomization, pragmatic clinical trials, etc.</p></li><li><p>Experience promoting teamwork, innovation, and motivation.</p></li><li><p>Experience estimating and planning resource needs and allocation.</p></li></ul><p>#GDBDMJobs</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 15:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Clinical Research Informatics]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R40950]]></requisitionid>
    <referencenumber><![CDATA[R40950]]></referencenumber>
    <apijobid><![CDATA[r40950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r40950/associate-manager-clinical-research-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>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. You will help us to organize, analyze and interpret health information aggregated from electronic health records, surveys, digital devices, and laboratory assays from multiple collaborators. This will require developing and implementing standards for health data as well as code repositories, pipelines and analysis tools that facilitate interacting with data.</p><p>You will need expertise in organizing and structuring large and complex datasets as well as top-notch software engineering and orchestration skills. You will help design data structures that store health data. You will implement the code and processes that populate, validate, and analyze these data. You will participate in the downstream analysis using machine learning, genomics, and epidemiology. This will be a dynamic, challenging position with lots of work and lots of opportunities.</p><p><strong>As an Associate Manager Clinical Research Informatics, a typical day might include</strong>:</p><ul><li><p>Developing and maintaining a toolkit with key functions, APIs, and summaries that help users understand, interpret, and interact with phenotype data. In addition to Python, knowledge of R, SQL and/or C++ is a definite plus.</p></li><li><p>Developing the tools and code that will transform electronic health records, surveys, laboratory assays, or digital device data into a harmonized tall and narrow format compatible with RGC analytical tools, applications and processes. You will probably be writing and updating code in Python and using associated data science libraries, such as pandas, Polars, NumPy, scikit, and others.</p></li><li><p>Reviewing the structure, content, and quality of phenotype data extracted from electronic health records, surveys, digital devices<strong>,</strong> or laboratory assays. Each of these datasets may include data on 100,000s of people and require coordination and input from multiple stakeholders with varied expertise.</p></li><li><p>Discussing the challenges and opportunities of using health data from electronic health records, surveys, digital devices<strong>,</strong> and laboratory assays to characterize human health and disease. Expertise in cutting-edge statistical methods for epidemiology is a definite plus.</p></li><li><p>Working with modern cloud environments and platforms. A knowledge of AWS and related toolkits will be useful for your day-to-day work. You will be using your computational skills to execute analysis and data processing at scale and to facilitate automation and repeatability of all key processes.</p></li><li><p>Presenting results and summaries of these datasets and data processing plans to a variety of technical audiences, ranging from experts in statistics, epidemiology, genetics, and computation to experts in biology, drug design, and medicine. You will need outstanding communication skills and an ability to summarize and present to a variety of technical audiences.</p></li><li><p>Working in a highly interactive environment with a team of colleagues. We highly value the ability to interact, learn, and teach so that you and other skilled individuals consistently achieve high levels of motivation, enthusiasm, and performance.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>A demonstrated knowledge of Python and key data science libraries is a must. Knowledge of R, SQL and/or C/C++ is also highly valued. If you have contributed to code in GitHub or another public repository, let us know.</p></li><li><p>Understanding strategies for mapping structured and unstructured data to ontologies such as ICD-10, RxNORM and LOINC.</p></li><li><p>Knowledge and experience applying best practices for data quality control, summarization and visualization.</p></li><li><p>A passion for learning. We are a fast-moving team in a fast-moving company. You should expect to encounter challenging work and to learn many new skills.</p></li></ul><p><strong>To be considered for this position </strong>you should have a PhD (or MS with additional years in lieu) in Computer Science, Health Informatics, Clinical Informatics, Biostatistics, or a related field with at least 0-2 years of relevant experience organizing large datasets in a research setting, whether in academia or industry, highly preferred.</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>$108,300.00 - $176,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Command Center Operations]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45898]]></requisitionid>
    <referencenumber><![CDATA[R45898]]></referencenumber>
    <apijobid><![CDATA[r45898]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45898/manager-command-center-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>We are currently looking to fill a Manager Operations Command Center position. In this role you will be responsible for the staff and processes associated with the monitoring and operation of campus MEP systems for all G&A and R&pD locations. These systems include but are not limited to BMS, HVAC, emergency power generation, UPS, critical lab equipment, site utility systems, etc. This position is responsible for the training and development of staff as well as the creation and revision of operating procedures for the center. Additionally, the Manager, Command Center Operations is expected to cultivate relationships with RE&FM leadership, property management leadership, and R&pD leadership. This position will be required to work holidays. Direct reporting structure may be simple or complex. (i.e. Direct reports may manage personnel or contract employees.</p><p>A typical day may include:</p><ul><li><p>Managing the Command Center Operations team</p></li><li><p>Developing processes and procedures for monitoring and/or response to onsite/offsite conditions in a multi-campus, multi-building environment</p></li><li><p>Responsible for contributing to and executing development plans for ROCC programs as well as direct reports</p></li><li><p>Performs administrative management responsibilities including timesheet review/approval, succession planning, candidate recruiting/interviewing, performance evaluation/feedback, etc.</p></li><li><p>Plan, schedule, and coordinate internally with Regeneron stakeholders and externally with outside contractors/vendors to perform scheduled and/or non-scheduled preventative/corrective maintenance/repair</p></li><li><p>Assists with negotiation of Master Service Agreements, Scope of Work contracts, and O&M contracts with Facilities Operations vendors</p></li><li><p>Participates in the design/installation/commissioning of disparate HVAC, BMS, Site Infrastructure, Lab Process systems with the capital project teams as required</p></li><li><p>Works closely with Business Continuity Team on disaster planning and emergency response strategy</p></li><li><p>Coordinates with RE&FM Leadership, Security, EHS, R&pD Operations, and Property Management during planned and unplanned events requiring broad communications and team synchronization</p></li><li><p>Collaborates with Asset Management & Property Management teams to ensure all MEP equipment is accurately represented in IWMS system</p></li><li><p>Ensure all relevant activities are documented accurately and promptly</p></li><li><p>Works with all relevant SOP’s</p></li><li><p>Provides specialized and/or general support when required to other departments</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Can operate company vehicles</p></li><li><p>Are available 24/7 for assistance and emergency response</p></li><li><p>Have the ability to work on diverse teams</p></li><li><p>Have advanced knowledge of commercial and industrial HVAC, BMS Control Sequences MEP principal and refrigeration</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Engineering or Facility Management/Operations Management or relevant field of study plus:</p><p>Manager Level: 8+ years of experience in relevant functions or industries. The ideal candidate will have in-depth Large campus commercial operations.</p><p>Relevant experience will be accepted in lieu of degree</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist - Allergy ENT (Jacksonville, Gainesville, Daytona)]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46175]]></requisitionid>
    <referencenumber><![CDATA[R46175]]></referencenumber>
    <apijobid><![CDATA[r46175]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46175/medical-specialist-allergy-ent-jacksonville-gainesville-daytona/]]></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[<p>Our Medical Specialists are at the forefront of engaging Allergists and Immunologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As an Allergy Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Market Access Pipeline]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46324]]></requisitionid>
    <referencenumber><![CDATA[R46324]]></referencenumber>
    <apijobid><![CDATA[r46324]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46324/director-market-access-pipeline/]]></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 has a rapidly expanding and diverse portfolio of investigational products, spanning across oncology, immunology, general medicine and rare diseases. To support the optimal clinical development and ensure the successful launch of these assets, we are recruiting a Director, Global Market Access Pipeline & Readiness, who will lead the market access planning for several assets in the pipeline.</p><p>This role requires a skilled strategist with excellent leadership capabilities to shape the direction of multiple pipeline assets. You will represent the payer voice for the assets you cover and will be accountable to define (and prepare for) successful reimbursement and patient access.</p><p>This role is part of the Market Access Pipeline & Readiness Team, which is part of the Market Access Business Unit. We are seeking a highly collaborative individual who will work cohesively within the cross-functional team that includes New Product (marketing), HEOR, Medical Affairs, Clinical and Regulatory. For programs that are nearing launch you will serve as the nexus between these stakeholders and other functions within the Inline Market Access Business Unit (Trade, Patient Support, Pricing) to ensure our launch plans reflect their expertise – ultimately leading to a smooth transition for launch.</p><p>Considering the growing Regeneron pipeline, company expansion and collaboration announcements, this role requires you to be comfortable operating autonomously within a growing and evolving company. You will be expected to proactively identify and resolve the opportunities and challenges to achieve the desired business objectives. This includes a commitment to working well together, which is a core value at Regeneron.</p><h3><strong>A typical day may include the following:</strong></h3><p>The Director of Market Access Pipeline & Readiness will work closely with the New Products (Commercial) Lead to inform the market access / payer perspective for key deliverables within the Development decision-making framework. Importantly, the Director will also be responsible for providing assumptions, and associated rationale, incorporated into program forecasts. Each member of the Market Access Pipeline & Readiness Team is assigned multiple assets that range from pre-phase one to filing. Therefore, specific accountabilities will vary by asset; you will be expected to:</p><ul><li>Incorporate timely payer insight and perspectives into commercial planning and clinical development for assets</li><li>Analyze trends and/or changes in the global market access environment, including competitors, to determine the strategic implications for the pipeline assets</li><li>Create and lead strategic market access and pricing plans for pipeline assets, with focus on US, EU and Japan</li><li>Ensure development plans will deliver a compelling payer value proposition(s) to achieve the target reimbursement</li><li>Advise cross-functional team on options for early engagement with HTA authorities with clear recommendations on the insight / knowledge gaps to address, then execute on recommendations</li><li>Identify clinical and economic evidence needs to achieve target reimbursement; ensure that there is a plan in place to address evidence gaps</li><li>Lead the development of market access tools for near-launch assets including global value proposition, objection handlers, launch readiness plans</li><li>Plan for early and expanded access programs in partnership with the development team and patient advocacy</li><li>Provide input as needed on internal needs (e.g., forecasting and business development initiatives)</li></ul><h3><strong>The role may be for you if:</strong></h3><ul><li>You bring a track record of building productive work relationships with internal partners</li><li>You can demonstrate initiative, critical thinking skills, and an ability to work effectively in complex, evolving environments</li><li>You are a strong project and process management skills; ability to work on multiple tasks and to effectively prioritize</li><li>You have lead a matrix team</li><li>You can effectively communicate in written and verbal communication globally</li></ul><p>To be considered for this role, we need you to have 12 years of industry progressive" industry/relevant professional experience in either consulting and/ or pharmaceutical/biotech with 2+ years of experience leading pipeline market access responsibilities. We believe you should have US and ex-US pharmaceutical market access experience of 5+ years with solid knowledge in building successful market access plans for key global payer systems (e.g. US, FRA, GER, UK). We are also looking for previous product launch experience in a market access role. Lastly, we require you to be onsite in Sleepy Hollow, NY for 4 days a week.</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager External Bulk Manufacturing]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45692]]></requisitionid>
    <referencenumber><![CDATA[R45692]]></referencenumber>
    <apijobid><![CDATA[r45692]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45692/manager-external-bulk-manufacturing/]]></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 fill a Mgr External Bulk Manufacturing position. The Mgr External Bulk Manufacturing strategically manages business relationships and/or facilitates day-to-day operations with Contract Manufacturing Organizations (CMOs) and Partners to achieve a consistently high level of interaction in order to meet or exceed Regeneron’s business needs relating to product quality, availability and delivery. Ensures that all critical external bulk manufacturing requirements are executed to ensure world-class performance of Industrial Operations & Product Supply (IOPS) product supply chains. The role of the Manager External Bulk Manufacturing is to act as the Relationship Lead with the CMO/Partners.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Ensures that product manufacture occurs in compliance with cGMP and applicable regulations.</p></li><li><p>Facilitates all External Bulk Manufacturing activities at contract and/or business partner manufacturing sites, including but not limited to scheduling of all batches, supply of materials, direct shipment of bulk and finished product at manufacturing site, tracking and monitoring cycle times and providing any required associated reports and technical expertise.</p></li><li><p>Forms strategic partnerships with technical and operational colleagues to effectively collaborate with other departments and contractors.</p></li><li><p>Functions as a liaison between Regeneron Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners.</p></li><li><p>Ensures the timely routine and review of all technical transfer activities, validation plans, master manufacturing records (MRs), standard operating procedures (SOPs) and other documentation needed to successfully execute required clinical and commercial external manufacturing activities at contractors and/or business partners.</p></li><li><p>Supports and informs strategic initiatives and contract negotiations that drive long-term relationship stability and success.</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>The Relationship Leads manage quarterly business review meetings or other governance structures with CMOs to drive continuous improvement in joint performance.</p></li><li><p>Resolves all supply issues with the CMO/Partner that affect product quality or availability, including evaluating cost/benefit scenarios, making sound recommendations and coordinating internal and external resources to address issues.</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>The Relationship Leads have overall responsibility for RFPs, project plans, purchase requisitions, etc. associated with contractor operations.</p></li><li><p>Provides regulatory filing support to IND, BLA, MAA, etc.</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><li><p>May manage direct report and/or lead a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.</p></li><li><p>May serve as the primary Regeneron technical contact for select contract manufacturing sites concerning day-to-day activities.</p></li><li><p>Travels to contract manufacturers or business partners, as required (25-50%).</p></li></ul><p>To be considered for the Associate Manager you must have a BS/BA in business or scientific discipline and 6 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</p><p>To be considered for the Manager you must have a BS/BA in business or scientific discipline and 7 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</p><p>To be considered for the Senior Manager you must have a BS/BA in business or scientific discipline and 8 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</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>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 17:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Oncology Skin Cancer Marketing]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46356]]></requisitionid>
    <referencenumber><![CDATA[R46356]]></referencenumber>
    <apijobid><![CDATA[r46356]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46356/director-us-oncology-skin-cancer-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[<p>The Director, US Oncology HCP Skin Cancer Marketing, is a member of the Oncology Business Unit with accountability for working closely with the Senior Director to develop commercial HCP promotion strategy and tactical plans for Non-Melanoma Skin Cancer (NMSC) within the US. Also responsible for collaborating with the International team for Global commercialization and promotion.</p><p>This position will report directly to the Senior Director, HCP Skin Cancer Marketing. The Director will work collaboratively across the Franchise Team, International teams, internal cross-functional colleagues, while effectively managing external agency partners to ensure alignment and to drive optimal integration and execution of personal and non-personal initiatives<strong>.</strong></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Lead HCP marketing for the NMSC indications in the US. This includes defining US market opportunities, analyzing the competitive landscape, identifying key site of care and key account segmentation and needs, developing customer-focused and differentiated product and indication positioning, and customizing messages to key target audiences.</li><li>Works in close collaboration with Clinical, Medical Affairs and Field Medical to ensure alignment with Medical Education strategic plans.</li><li>Engage with physician experts and attend key congresses to support Scientific Marketing team efforts and assess important disease and treatment data.</li><li>Work closely with the Insights and Data Analytics team to design and implement promotional strategies, while tracking brand performance, share of voice, market dynamics and competitive actions & response. Provide business assumptions input to forecasting.</li><li>Oversee and collaborate with Digital/Media Strategy team for optimization and implementation of the multi-channel marketing mix, including omni-channel digital & media strategy and implementation, and creation and deployment of educational resources towards brand objectives and developing indicators/metrics for high-impact engagements with HCP key target audiences.</li><li>Develop and coordinate NMSC HCP Marketing inputs and key sections of brand plan, identify and prioritize business opportunities.</li><li>Responsible for the development of the Field Plan of Action and training plan, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/collaborators.</li><li>Maintain strong collaborative relationships with cross-functional areas and internal strategic partners (i.e., Field Sales, Training, Promotional Review Committee, Medical Affairs, Regulatory, Clinical, Legal, Compliance, Market Access etc.)</li><li>Ensures that the marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines.</li><li>Manages and develops a direct report to ensure their continued development and growth.</li><li>Works cross functionally to create, manage and track budget to ensure operating within the approved budget and phasing.</li></ul><h3><strong>This job might be for you if:</strong></h3><ul><li>You are effective collaborator and communicator both written and verbal</li><li>You can navigate regularly in ambiguity</li><li>You excel in a fast paced environment</li></ul><p>To be considered for this role, we expect you to have a Bachelors degree is required; 12+ years of pharmaceutical marketing focused on Oncology. Along with leading and developing long range brand plans, budgets and forecasts for commercial teams in the pharmaceutical/biotech industry. Lastly, this role requires you to travel 30% of the time and to be in the office in Sleepy Hollow, NY 4 days a week.</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Technical Analyst - Manufacturing Systems]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45572]]></requisitionid>
    <referencenumber><![CDATA[R45572]]></referencenumber>
    <apijobid><![CDATA[r45572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45572/principal-technical-analyst-manufacturing-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal Technical Analyst - Manufacturing Systems will serve as a technical expert responsible for implementing and integrating manufacturing technologies across our biopharmaceutical facilities. You will execute hands-on technical builds and integrations spanning Nymi biometric systems, IBM Maximo EAMS (Enterprise Asset Management System), and related manufacturing technologies, ensuring compliant deployment that supports operational excellence and predictive maintenance capabilities.</p><p>As a Principal Technical Analyst - Manufacturing Systems , a typical day might include the following:</p><p>Technical Implementation & Integration</p><ul><li>Execute technical builds and integrations for manufacturing systems including Nymi biometric authentication, IBM Maximo EAMS, MES platforms, and associated technologies across designated facilities or project portfolios</li><li>Implement integration solutions connecting Maximo with predictive maintenance systems, MES workflows, and biometric access controls, following established architectural frameworks</li><li>Configure IBM Maximo EAMS modules including work management, asset management, and predictive maintenance capabilities for future release implementations</li><li>Build and test Nymi biometric integration points with manufacturing systems to enable secure, compliant user authentication workflows</li></ul><p>Compliance & Validation Support</p><ul><li>Execute validation protocols (SDLC Framework aligned to CSA) for manufacturing technology implementations in FDA-regulated environments, ensuring documentation meets regulatory standards</li><li>Implement change control procedures for system modifications, maintaining compliance throughout the development lifecycle</li><li>Configure master data elements within assigned systems following established data architecture standards</li><li>Support transformation of paper-based processes into digital workflows while maintaining regulatory compliance requirements</li></ul><p>Technical Problem Resolution</p><ul><li>Troubleshoot and resolve technical issues related to system integrations, connectivity challenges, and performance optimization across multiple manufacturing technology platforms</li><li>Diagnose integration problems between Maximo, biometric systems, MES platforms, and automation equipment (Ignition, DeltaV, Rockwell)</li><li>Implement technical solutions under timeline constraints while maintaining quality and compliance standards</li><li>Document technical issues, root cause analysis, and resolution approaches for knowledge sharing</li></ul><p>Collaboration & Support</p><ul><li>Partner with senior technical leads, automation engineers, and site stakeholders to understand requirements and deliver technical solutions aligned with business objectives</li><li>Provide technical expertise to project teams implementing new manufacturing technologies or system upgrades</li><li>Contribute to the development of technical standards, build procedures, and integration patterns for the IOPS IT Manufacturing Build team</li><li>Support knowledge transfer activities and mentor junior team members on specific technical implementations</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field required along with </p><p>Principal: 8+ years of progressive industry/relevant experience </p><p>Staff: 10+ years of progressive industry/relevant experience </p><p>May consider equivalent combination of education and experience. Level is 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 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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 14:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)]]></title>
    <date><![CDATA[Sat, 20 Sep 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42074]]></requisitionid>
    <referencenumber><![CDATA[R42074]]></referencenumber>
    <apijobid><![CDATA[r42074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42074/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[<div><p>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. This role may work on studies in melanoma, lung, breast, gastric, or colorectal cancers.</p></div><div><p><strong>As a Medical Director, a typical day may include the following:</strong></p><ul><li><p>Defines clinical trial-related goals and objectives.</p></li><li><p>Conducts literature and database research on clinical trials as needed</p></li><li><p>Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.</p></li><li><p>Leads and supervises the Clinical Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role may be for you if:</strong></p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p><br><strong>To be considered for this role</strong>, you must have a MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience. Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.</p><div><p><em>This role has a 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ.</em></p></div><div><div><div><div></div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, PV Enablement]]></title>
    <date><![CDATA[Thu, 20 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43336]]></requisitionid>
    <referencenumber><![CDATA[R43336]]></referencenumber>
    <apijobid><![CDATA[r43336]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43336/director-pv-enablement/]]></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>Regeneron's Global Patient Safety Organization is looking for a Director, PV Enablement to join the team!!</p><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>The Director of PV Enablement will report directly to the VP of Global Patient Safety (GPS) Operations. This role is pivotal in shaping the delivery of pharmacovigilance (PV) governance to ensure operational requirements are met within a growing global PV platform.</p></li><li><p>In coordination with the Vice President (VP) of GPS Operations, provide strategic oversight and deliver global PV governance in partnership with the GPS Leadership Team (GPS LT). </p></li><li><p>Develop and maintain operational reporting dashboards and provide status oversight for key GPS project initiatives in collaboration with the VP of GPS Operations. </p></li><li><p>Partner with cross-functional teams, including Development Operations, Portfolio Management, and Biostatistics/Data Management, to establish operational portfolio forecasting for GPS.</p></li><li><p>Offer strategic, holistic support for GPS interfaces to enable PV operations and ensure alignment across functions. </p></li><li><p>Lead operational excellence optimization activities, including benchmarking PV innovation and capabilities, as assigned. </p></li><li><p>Identify and assess operational risks across all areas of GPS, ensuring proactive mitigation strategies are in place.</p></li></ul><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>This enablement role is accountable for demonstrating pharmacovigilance (PV) technical expertise and leadership, working collaboratively with key stakeholders to perform the following essential functions:</p></li><li><p>Strategic PV Operations Oversight and Governance: In coordination with the Vice President (VP) of GPS Operations, provide strategic oversight and ensure the effective delivery of global PV governance within the Global Patient Safety (GPS) organization and leadership team. </p></li><li><p>Operational Reporting and Forecasting: Implement an operational reporting dashboard and oversee the status of key GPS project initiatives by partnering with the VP of GPS Operations to ensure the effective delivery of portfolio requirements. Collaborate with cross-functional teams—including Development Operations, Portfolio Management, and Biostatistics/Data Management—to establish operational portfolio forecasting.</p></li><li><p>Support for GPS Interfaces: Offer strategic and holistic support to GPS interfaces to enable PV operational alignment and effectiveness. </p></li><li><p>Operational Excellence: Lead operational excellence initiatives, including benchmarking PV innovation and capabilities, as assigned. Holistically identify and assess GPS operational risks, supporting inspection readiness in collaboration with team stakeholders and relevant areas. </p></li><li><p>Regulatory Compliance and Safety Initiatives: Ensure the successful execution of safety initiatives, maintain regulatory compliance, and drive continuous process improvements within the GPS organization. </p></li><li><p>Cross-Functional Collaboration: Act as a key liaison between the PV department and other functions, including Regulatory Affairs, Development Quality, and Regeneron. </p></li><li><p>Resource Management and Operational Planning: Provide strategic oversight to develop and implement resource management plans, focusing on efficiency of operational requirements within GPS.</p></li><li><p> Planning and Execution Improvement: Oversee and apply a systematic approach, using structured methodologies, to continuously improve planning processes and operational execution. Identify strategic priorities in partnership with the VP to optimize workflows, maximize delivery efficiency, and enhance overall effectiveness. </p></li><li><p>Operational Optimization and Broader Partnerships: Actively participate in operational optimization activities by collaborating with Regulatory Affairs, Global Patient Safety, Development Quality, and Global Development teams. </p></li><li><p>Leadership and Team Development: Manage ambiguity and translate challenges into tangible outputs and opportunities for the department. </p></li><li><p>Contribute to an enriching team environment that supports GPS culture, capability growth and team development, both as a team member and individually, in alignment with the values of the Regeneron Way. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum Bachelor's Degree 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>Function as a subject matter expert in global pharmacovigilance for GPS operations and planning.</p></li><li><p>A 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 problem-solving with the ability to “flex” across different complexities, business situations and cross functional partners of global patient safety</p></li><li><p>Success in effectively utilizing PV technical expertise along with communicating and influencing decisions with all levels of an organization and delivering high quality work.</p></li><li><p>Demonstrated ability and track-record to lead PV operational and planning initiatives with excellence, including governance activities.</p></li></ul><p>#GDPSJobs</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>$202,000.00 - $336,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist- Albuquerque NM, Amarillo, Lubbock TX]]></title>
    <date><![CDATA[Mon, 17 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43551]]></requisitionid>
    <referencenumber><![CDATA[R43551]]></referencenumber>
    <apijobid><![CDATA[r43551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43551/oncology-account-specialist-albuquerque-nm-amarillo-lubbock-tx/]]></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: Albuquerque NM, Amarillo, Lubbock TX</strong></p><p>The Oncology Account Specialist, NSCLC and NMSC will engage specific NSCLC & NMSC (including CSCC and BCC) Oncology specialists and key Oncology customers within a specific account 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, Regional Science Managers to efficiently and effectively address customer needs.</p><br><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Engage Oncology Specialists (NSCLC and NMSC) and other key experts within assigned account alignment and deliver clinical messages to introduce the launch of the brand in NSCLC & NMSC (including CSCC and BCC), grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, alliance counterpart(s), 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 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 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). Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC & NMSC (including CSCC and BCC) 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 Oncology NSCLC & NMSC (including CSCC and BCC) 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. <strong>Must live in the territory.</strong></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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Reporting and Analytics Lead (Oracle Fusion)]]></title>
    <date><![CDATA[Thu, 18 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44208]]></requisitionid>
    <referencenumber><![CDATA[R44208]]></referencenumber>
    <apijobid><![CDATA[r44208]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44208/director-erp-reporting-and-analytics-lead-oracle-fusion/]]></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 Oracle Fusion ERP Reporting and Analytics Lead oversees the reporting and analytics strategy for the Oracle Fusion Cloud implementation. This role partners closely with SI partners, GPOs, Product Leads, Data Engineering, and Business SMEs to rationalize reporting requirements and guide the design and development of reporting solutions across Oracle Fusion Cloud reporting tools and Fusion Data Intelligence (FDI). The role ensures that reporting architecture, data sourcing, and analytics approaches align with enterprise standards, support phased modernization—from Oracle EBS to Oracle Cloud—and comply with data governance and AI policies, including the responsible use of Oracle AI Agents.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide leadership and subject-matter expertise across Oracle Fusion Cloud reporting tools, including OTBI, BI Publisher, Fusion Data Intelligence (FDI), OAC within FDI, Financial Reporting Center, Account Inspector/Monitor, Smart View, and embedded dashboards/KPIs.</p></li><li><p>Work closely with the SI partner to guide reporting design, validate deliverables, and ensure solutions meet business requirements and align with Oracle Cloud capabilities.</p></li><li><p>Lead the report rationalization strategy, determining the appropriate placement of reporting across Fusion-native tools, FDI, the Data Lake, or external BI platforms.</p></li><li><p>Support reporting strategy across a phased implementation, where some functions transition to Oracle Fusion Cloud while other modules remain in Oracle EBS.</p></li><li><p>Ensure reporting continuity during Chart of Accounts (CoA) redesign, including mapping, harmonization, and alignment of reporting structures across EBS and Oracle Cloud during coexistence.</p></li><li><p>Guide reporting solutions that require combined data from Fusion Cloud and external systems, determining where best to perform data blending (FDI vs. Data Lake).</p></li><li><p>Oversee Data Lake extract designs and data sourcing strategies, ensuring required datasets from Oracle Cloud and legacy systems are modeled accurately and consistently.</p></li></ul><h3><strong>This Job Might Be For You If You Have:</strong></h3><ul><li><p>Deep expertise with Oracle Fusion Cloud reporting tools: OTBI, BIP, Fusion Data Intelligence (FDI), OAC within FDI, Financial Reporting Center, Account Monitor/Inspector, Smart View, and embedded KPIs.</p></li><li><p>Strong ability to rationalize reporting requirements and determine appropriate placement across Fusion-native tools, FDI, Data Lake, or external BI platforms.</p></li><li><p>Ability to guide SI partner designs and influence architectural decisions.</p></li><li><p>Knowledge of key business domains including P2P, R2R, O2C, Plan to Make, PLM/PDH, WMS, OTM/GTM.</p></li><li><p>Experience designing, reviewing, and governing Standard and Custom Oracle AI Agents for reporting and analytics use cases.</p></li><li><p>Strong knowledge of SOX, audit controls, data integrity, and security/role-based access models.</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>Bachelor’s degree in Information Systems, Data Analytics, Computer Science, Engineering, or related field.</p></li><li><p>15+ years of experience in enterprise reporting and analytics.</p></li><li><p>10+ years of experience with Oracle Fusion Cloud reporting tools.</p></li><li><p>3+ years of experience with Oracle AI Agents.</p></li><li><p>Experience supporting large-scale ERP transformations and phased modernization (EBS → Fusion)</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[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Pricing Strategy - Immunology]]></title>
    <date><![CDATA[Sun, 11 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44452]]></requisitionid>
    <referencenumber><![CDATA[R44452]]></referencenumber>
    <apijobid><![CDATA[r44452]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44452/senior-director-pricing-strategy-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>The Senior Director, Pricing Strategy, Immunology plays a critical role at Regeneron as they will serve as the primary point for Immunology Global (Ex-US) for inline and LCM indications across all International Markets as well as Immunology pipeline assets. This position is heavily focused on leading the evolution of global pricing strategies to ensure the continued long-term commercial success across multiple indications and geographies. This role will require deep expertise in ex-US payer archetypes, pricing dynamics, and cross-functional collaboration to optimize pricing strategies in alignment with regulatory, payer, and market needs. The ideal candidate will bring strong leadership, analytical, and strategic skills to drive pricing excellence in a highly competitive and dynamic environment.</p><h3>A Typical Day Includes:</h3><ul><li>Serve as a trusted advisor to key partners on Global Pricing risks and opportunities as the Primary Subject Matter Expert for Immunology</li><li>Lead the Pricing Governance process and make go/no-go reason recommendations to senior leadership in partnership with key Market Access and Commercial team members</li><li>Provide strategic inputs and conduct analytics on market-specific price proposals to support the Global Pricing Committee process</li><li>In partnership with Market Access & HEOR, define and implement the global pricing strategy for Immunology assets across all phases—from clinical development through commercialization</li><li>Lead all primary and secondary research and financial analytics to support an insights driven value-based Pricing Strategy</li><li>Lead cross-functional pricing strategy teams, integrating insights from Market Access, HEOR, Medical Affairs, and Commercial functions</li></ul><p><strong>This Role May be for you:</strong></p><ul><li>You have strong leadership, excellent communication and presentation skills with a strategic perspective and the ability to influence without authority</li><li>You bring experience in specialty required with Immunology experience a plus</li><li>You leverage knowledge of pricing market research tools, methodologies, and analytics including exposure to global price management systems</li><li>You can work independently and collaboratively in a matrix team environment</li><li>You thrive is a fast-paced environment and manage multiple projects</li><li>You bring a positive attitude, take-charge mentality, and solution oriented</li></ul><h3>To be considered, you must possess:</h3><ul><li>Advanced degree required (MBA, MPH, PharmD, MHA, or related field)</li><li>15+ years of progressive experience in US & Global Pricing, Market Access, or Commercial Strategy within the biopharmaceutical industry</li><li>Strong understanding of both US Payer System (Commercial, Medicare, & Medicaid), and Ex-US/International (EU4, UK, and other major markets) in terms of Payer, Provider, and Patient dynamics</li><li>Demonstrated experience with managing inline assets and developing global launch pricing strategies (launch sequencing) in the context of various HTA archetypes and payer systems</li><li>Strategic Leader with exceptional analytical and financial modeling skills with a global perspective</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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Jan 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Scientific Marketing Neurology]]></title>
    <date><![CDATA[Thu, 29 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44932]]></requisitionid>
    <referencenumber><![CDATA[R44932]]></referencenumber>
    <apijobid><![CDATA[r44932]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44932/senior-director-scientific-marketing-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>The Senior Director of Scientific Marketing Neurology is a member of Regeneron’s Neurology commercial team, with accountability in leading all professional medical education commercial activities in support of the launch and commercialization in Myasthenia Gravis in the US.</p><p><strong>In this position a typical day may include the following:</strong></p><p>Responsible for Peer to Peer promotional education strategy, planning and execution</p><ul><li>Promotional speaker program execution including live, webex, launch meeting, broadcast events.</li><li>Speaker bureau management and speaker training.</li><li>Development and roll out of promotional content for speaker programs and other peer to peer programs.</li><li>Promotional med com agency management.</li><li>Sales force communication for peer to peer programming and alignment with all cross functional teams.</li></ul><p>Responsible for developing US and select Global Congress plan and execution including congress displays (booths/table tops), partner engagement plan, advertising plan, competitive intelligence, logistics and coordination with cross functional teams.</p><ul><li>Responsible for KOL identification, mapping and engagement plan.</li><li>Lead the development/management of relationships with KOL’s, key HCP’s and professional partners.</li><li>Development and execution of US commercial advisory boards to inform and support brand strategy.</li><li>Manage and coordinate local and regional Neurology trade shows and scientific meetings.</li><li>Develop and manage promotional and advertising spend across the different programs.</li><li>Provide support to the development of the overall brand strategy, functional plans and budget.</li></ul><p><strong>This May Be the Right Role for You If you:</strong></p><ul><li>You bring a track record of commercial success in positions with progressive responsibilities.</li><li>You have effective communication, both written and oral, at all times. Experience in delivering complex messages to various internal and external customers with a track record of effective and influential presentations.</li><li>You demonstrate initiative, creativity, strategic capabilities, and ability to work effectively in complex, rapidly changing environments.</li></ul><h3>To be considered for this role</h3><ul><li>Minimum of 12 years biopharmaceutical experience with at least 7 in Marketing</li><li>Previous product/indication launch experience required.</li><li>Strong science background with deep knowledge of Rare Neurology or Myasthenia Gravis. Ability to understand, work with, and provide commercial input to all functions within the project team.</li><li>Bachelor's Degree Required, MBA 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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 30 Jan 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology- Fresno, CA]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45035]]></requisitionid>
    <referencenumber><![CDATA[R45035]]></referencenumber>
    <apijobid><![CDATA[r45035]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45035/medical-specialist-i-dermatology-fresno-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fresno]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Fresno, California</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - B’ham, Black Country, Staffs, Shropshire, Telford & Wrekin]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45110]]></requisitionid>
    <referencenumber><![CDATA[R45110]]></referencenumber>
    <apijobid><![CDATA[r45110]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45110/sales-specialist-b-ham-black-country-staffs-shropshire-telford-wrekin/]]></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 B’ham, Black Country, Staffs, Shropshire, Telford & Wrekin 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>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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44959]]></requisitionid>
    <referencenumber><![CDATA[R44959]]></referencenumber>
    <apijobid><![CDATA[r44959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44959/senior-manager-global-patient-safety-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>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><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</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 might be for you if can/have the:</strong></p><ul><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><strong>To be considered for this opportunity, you must have the following:</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></ul><p>#GDPSJobs </p></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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Quality Assurance]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44609]]></requisitionid>
    <referencenumber><![CDATA[R44609]]></referencenumber>
    <apijobid><![CDATA[r44609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44609/vice-president-quality-assurance/]]></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>Regeneron is hiring! The Vice President, Quality Assurance will lead the strategic development, execution, and oversight of key quality and compliance programs across Regeneron GMP operations. This role blends deep expertise in microbiology, data governance, and quality systems to safeguard patient safety, ensure product effectiveness, and uphold global regulatory compliance. This position will guide cross-functional teams, drive innovation, and champion a culture of quality across the organization. </p><p>In this role, a typical day might include the following:</p><p>Microbiology Program Leadership:</p><ul><li><p>Oversee the development and implementation of a value-added microbiology program aligned to global regulatory and legal requirements.</p></li><li><p>Monitor program performance via metrics; embed quality tools and risk management for continuous improvement.</p></li><li><p>Stay ahead of evolving industry standards and proactively adapt program strategy and execution.</p></li><li><p>Make science-based decisions that protect patient safety and ensure product quality and effectiveness.</p></li><li><p>Act as a microbiology decision-maker with internal stakeholders, regulators, and corporate partners.</p></li><li><p>Partner with lines of business to drive operational performance and compliance.</p></li><li><p>Allocate resources and set high-performance standards to meet microbiological and organizational objectives.</p></li></ul><p>Data Governance & Integrity (DGI) Program Leadership:</p><ul><li><p>Lead strategic vision of the of the DGI Program, including engagement, culture, monitoring, and operational leadership.</p></li><li><p>Develop and implement policies and procedures aligned with global regulatory standards and industrial best practices.</p></li><li><p>Drive a mature data quality culture through change management and stakeholder engagement.</p></li><li><p>Ensure DGI standards are continuously met and the function is properly resourced and equipped.</p></li></ul><p>Quality Systems Oversight:</p><ul><li><p>Establish and lead quality systems across Regeneron with clear roles, responsibilities, workflows, and metrics.</p></li><li><p>Provide leadership, tools, and coaching to quality system owners for effective execution.</p></li><li><p>Oversee Right to Operate Review meetings; ensure management review expectations are met.</p></li><li><p>Represent the Quality Management System Office in initiatives and program meetings, aligned to organizational goals.</p></li><li><p>Coach and mentor staff; collaborate with Information Systems to support quality systems and the Quality Plan.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven expertise in microbiology, data governance, and quality systems within GMP environments.</p></li><li><p>Experience leading enterprise quality transformations across multi-site operations.</p></li><li><p>Familiarity with digital quality systems, data analytics, and industry best-in-class tools.</p></li><li><p>Strong knowledge of global regulatory standards and quality management principles.</p></li><li><p>Demonstrated ability to drive change management and foster a culture of quality and compliance.</p></li><li><p>Skilled in resource allocation, strategic planning, and decision-making in complex technical and regulatory settings.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and 20+ years in a GMP-regulated industry (Biotech, Pharma, Medical Device), including at least 5+ years in a managerial capacity, or equivalent education and experience.</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>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Detroit]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44984]]></requisitionid>
    <referencenumber><![CDATA[R44984]]></referencenumber>
    <apijobid><![CDATA[r44984]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44984/medical-specialist-i-dermatology-detroit/]]></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[<p><strong>Geography: Detroit, Michigan</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Sales Project Manager]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45475]]></requisitionid>
    <referencenumber><![CDATA[R45475]]></referencenumber>
    <apijobid><![CDATA[r45475]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45475/senior-sales-project-manager/]]></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>We are Regeneron,</strong> a leader in innovative biotechnology, and we are looking for a passionate Senior Sales Project Manager to join our growing team in Tokyo, Japan. This is a unique opportunity to play a pivotal role in shaping the success of our sales strategies and partnerships within the Japanese market. As a key member of our Japan Commercial Operations team, you will drive strategic initiatives, foster collaboration across alliances, and contribute to meaningful advancements in specialty care. Join us to lead impactful projects and help improve lives through innovation.</p><div></div><p><strong>A Typical Day:</strong></p><ul><li>Lead the design, planning, and execution of strategic sales initiatives to align with business objectives.</li><li>Oversee advanced analytics, refining segmentation and targeting strategies to provide actionable insights.</li><li>Act as a senior escalation point, ensuring smooth communication between sales teams, stakeholders, and alliances.</li><li>Facilitate high-level meetings, setting strategic agendas and documenting key decisions for the Japan Leadership Team.</li><li>Manage cross-functional and alliance projects, ensuring timely delivery of results.</li><li>Develop team members while fostering a culture of high performance and continuous improvement.</li><li>Identify and address operational risks, collaborating with global and regional teams to ensure market success.</li><li>Represent Regeneron in alliance communications and external engagements, building strong relationships with key partners.</li></ul><div></div><p><strong>This Role May Be For You If You:</strong></p><ul><li>Have a proven track record in pharmaceutical marketing and sales management, especially within specialty care in Japan.</li><li>Excel at analyzing complex KPIs and providing strategic insights to senior stakeholders.</li><li>Thrive in a collaborative environment, effectively coordinating cross-functional teams and alliances.</li><li>Are proactive, strategic, and detail-oriented, with exceptional planning and organizational skills.</li><li>Possess strong interpersonal and communication skills, adeptly managing both internal and external stakeholders.</li><li>Enjoy driving innovation and operational excellence in a dynamic market environment.</li></ul><div></div><p><strong>To Be Considered:</strong></p><p>You must have a business or life sciences degree, fluency in Japanese, and business-level English proficiency. A minimum of 5 years of progressive industry experience, including 3+ years in pharmaceutical or biotech marketing, is required. Experience in immunology, biologics, dermatology, respiratory, or rhinology is preferred, along with prior co-promote or alliance work. Launch experience is a plus.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 02:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Toledo and Dayton, OH]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44994]]></requisitionid>
    <referencenumber><![CDATA[R44994]]></referencenumber>
    <apijobid><![CDATA[r44994]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44994/medical-specialist-i-dermatology-toledo-and-dayton-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dayton]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Toledo and Dayton, OH</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Predictive Analytics]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45118]]></requisitionid>
    <referencenumber><![CDATA[R45118]]></referencenumber>
    <apijobid><![CDATA[r45118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45118/senior-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>We are seeking a highly motivated and talented Senior Manager of Predictive Analytics to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop and apply predictive models 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. The candidate must have the ability to influence, with strong interpersonal skills. Excellent communication and interpersonal skills are also required as this candidate will be expected to work productively in a collaborative, team working environment.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Plan, develop, and execute large-scale analyses of proteomic and genomic datasets, with an emphasis on aging and age-related diseases.</p></li><li><p>Develop and implement methods for data harmonization and normalization across distinct cohorts to ensure consistency and reproducibility of results.</p></li><li><p>Evaluate statistical methods for disease risk prediction, and if necessary, develop new methods</p></li><li><p>Turn disease prediction needs 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 research directions</p></li><li><p>Deliver clear and concise presentations of genomics and proteomic findings to leadership, ensuring alignment with organizational goals and priorities</p></li><li><p>Ability to provide data to internal, external, and non-scientific audience </p></li><li><p>Design, implement, and optimize data pipelines for high-throughput genomic and proteomic workflows, ensuring efficient processing of large-scale proteomic datasets.</p></li><li><p>Develop and integrate robust quality control (QC) measures at multiple stages of analysis pipelines to ensure data accuracy, consistency, and reproducibility.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Demonstrated expertise in statistics, machine learning and predictive analytics applied to biological data.</p></li><li><p>Demonstrated aptitude for translating research results into products or prototypes</p></li><li><p>Proven ability to independently lead and manage 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>Demonstrated ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li><p>A PhD in a relevant field (e.g., human genetics, statistics, computational biology, or related disciplines) and at least five years of experience analyzing large-scale genomics data, or a bachelor's degree with at least 8 years of relevant experience.</p></li><li><p>Candidates with prior industry experience are preferred</p></li><li><p>Experience in exploratory data analysis, applied statistics, or software engineering is preferred in one or more of these domains</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 19:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Procurement - Direct]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45462]]></requisitionid>
    <referencenumber><![CDATA[R45462]]></referencenumber>
    <apijobid><![CDATA[r45462]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45462/associate-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>We are currently looking to fill an Associate Director Global Procurement, Direct position within our team. In this role you will develop a holistic Category Strategy and provide strategic leadership and direction with a focus on Packaging Components and Device Category. This role will work closely with stakeholders to lead discussions related to Packaging Components and Device Categories while aligning priority needs with procurement management and stakeholders. This position will be critical to driving performance across the IOPS External Manufacturing categories including alignment with stakeholder goals, driving towards competitive advantages (strategic and financial) and optimizing supplier relationships. This role works in close collaboration with IOPS Stakeholders to enable company revenue targets and the new product pipeline.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Help define and implement the global Packaging Components and Devices Category strategy to serve global and regional business needs.</p></li><li><p>Manage negotiations, supplier management activities, and stakeholder engagement activities for the Packaging Components and Devices Category as assigned.</p></li><li><p>Work with leadership to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Represent Global Procurement by participating in organizational decisions in the Packaging Components and Devices categories with critical short and long-term impact on the success, efficiency, growth, and results of Global Procurement.</p></li><li><p>Demonstrate knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Manage category activities to ensure compliance with appropriate GxPs and other applicable regulations, as applicable.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li><li><p>May provide coaching and guidance on job performance and career development to direct reports (if applicable) and provides leadership examples for the organization.</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Believe that value can be driven through strategic partnerships and efficient ways of working.</p></li><li><p>Can tap into strong in-depth knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of a Global Procurement organization.</p></li><li><p>Enjoy successfully leading global categories or global teams, processes, and suppliers within a multi-national organization.</p></li><li><p>Serve as role-model leader consistently exhibiting behaviors across an organization of direct reports to create clarity, provide a clear and understandable vision with transparency and trust both within and outside of the organization.</p></li><li><p>Can demonstrate success managing cross-functional teams to drive results in Packaging Components and Devices categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Can influence and partner with senior executives and peer functions to drive strategic change and efficiency.</p></li><li><p>Have working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Have experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><ul><li><p>Director: 10+ years of experience in relevant functions or industries. The ideal candidate will have in-depth knowledge of Packaging Components and Device Category experience.</p></li></ul><p> This role requires working onsite 5 days per week.</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>$147,800.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 08:56:27 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Dayton, OH/Northern Cincinnati]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45789]]></requisitionid>
    <referencenumber><![CDATA[R45789]]></referencenumber>
    <apijobid><![CDATA[r45789]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45789/medical-specialist-i-pulmonology-dayton-ohnorthern-cincinnati/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dayton]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Dayton, OH/Northern Cincinnati -representative must reside within or close to the territory.</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>As a Medical Specialist, a typical day might include the following:</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 may be for you if you:</strong></p><ul><li><p>Are confident in demonstrating strong and consistent sales performance that exceeds expectations related to goals</p></li><li><p>Are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>Can demonstrate a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>Collaborate effectively with internal and external partners</p></li><li><p>Share a passion and learning interest in science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li></ul><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. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. 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. Ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 09:56:45 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Mgr Clinical Database Development]]></title>
    <date><![CDATA[Sun, 22 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42998]]></requisitionid>
    <referencenumber><![CDATA[R42998]]></referencenumber>
    <apijobid><![CDATA[r42998]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42998/mgr-clinical-database-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>Manager, Clinical Database Development </strong><strong>(Tarrytown, NY)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks a Manager, Clinical Database Development (Tarrytown, NY) to oversee the development and/or technical activities for EDC databases built by CRO partners for assigned studies. Ensure all database build activities are performed according to Regeneron Processes (or CRO processes where applicable). Contribute to the creation of CDASH compliant eCRFs. Maintain and contribute to company standard Global Library. Perform Clinical Database Development activities for all assigned studies. Build early to late phase studies in Medidata Rave independently based on portfolio needs. Provide advanced expertise on Rave database builds to CROs and internal REGN teams. Under direction, support inspection activities related to RAVE and Clinical Database Development. Support the implementation of Database Development strategies for REGN acquisitions. Lead or contribute to special projects that require EDC input. Contribute to Database Development operational meetings with DM CRO partners. Train DM CRO partners on Database Development best practices and REGN requirements. Fulfill the SME role for 1 or more topics. Develop and deliver training. Provide ongoing support for Data management and key stakeholders (as applicable). Track milestones/deliverables, escalate and follow resolution as necessary, and communicate portfolio level updates to internal and CRO developers. Assist in the development of SOPs, Work Instructions, Guidance Manuals, and other Database Development tools. Recommend areas for improvement in Database Development process and practice. Mentor junior staff members. Telecommuting permitted. 20% domestic travel for client meetings, training, conferences, or other business-related activities.</p><p>SALARY: $142,958.00 - $184,700.00 per year</p><p><strong>Job Requirements:</strong></p><p>Requires a Bachelor’s degree in Information Technology or related field and 3 years of direct and indirect Rave EDC database development experience. Must have experience with: Medidata Rave; C# programming; SAS programming; Programming in Electronic Data Capture (EDC), Good Clinical Practice (GCP), and Medidata Rave; Programming languages like SAS, PL/SQL, C# and Microsoft office suite (Word, Excel, and PowerPoint); Providing guidance on Rave database builds to CROs and internal teams; 21 CFR Part 11, ICH-GCP Guidelines and CDISC standards for data collections; Data Management and Database; Rave URL and database related upgrades; and Creating SAS programs for data extraction and compliance checks. Must have a Medidata Study Builder Certification. 20% domestic travel for client meetings, training, conferences, or other business-related activities..</p><p>Apply at https://careers.regeneron.com; Reference code: R42998</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 14:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp QC Technical Resources Specialist]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45769]]></requisitionid>
    <referencenumber><![CDATA[R45769]]></referencenumber>
    <apijobid><![CDATA[r45769]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45769/temp-qc-technical-resources-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Within this role you will support lifecycle management within the QC Technical Resources group. You will participate (Perform, Review, Co-ordinate) in assay development, characterization, optimization, transfer, validation and investigation for QC group. You may provide technical support, guidance and supervision for release, stability, and in-process testing and assay development as a subject matter expert (SME).</div><div></div><div>Please note this is a 12-month contract position.</div><div></div><div></div></div><p><strong>As a Temp QC Technical Resources Specialist</strong><strong>, a typical day might include, but is not limited to, the following:</strong> </p><ul><li>Collaborating with Analytical Sciences (AS) to integrate methods into QC Commercial evaluating and selecting suitable methods prior to process validation</li><li>Monitoring and analyze daily method performance in the QC lab, coordinating with subject matter experts for problem resolution as needed</li><li>Liaising with Regulatory Sciences and External Manufacturing to manage timelines for method validation and transfers, communicating updates to management</li><li>Monitoring method updates, performance, and quality metrics, ensuring consistent harmonization and performance evaluations across multiple sites</li><li>Coordinating post-transfer investigations and multi-site trending, escalating issues to management when necessary</li><li>Driving process improvements and support investigational analysis, performing and coordinating assay qualifications and transfers</li><li>Developing and drafting new test procedures and assays, authoring technical documents like Analytical Development and Validation Reports</li><li>Participating in training programs for QC personnel, ensuring all activities align with project timelines and deliverables<br> </li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>The ability to work independently or as part of a team</li><li>Strong skills in planning, critical thinking and problem-solving, ability to follow directions and perform well-defined tasks</li><li>Excellent written and oral communication skills</li><li>The ability to develop strategy and create metrics to measure effectiveness of strategy</li></ul><p>To be considered for this opportunity you should have a BS/BA in a life sciences field and 2 years of experience or equivalent combination of education and experience.</p><p>Scientist level minimum 2 years of experience</p><p>Sr Scientist level minimum 5+ years of experience<br><br>#LI-Onsite #JOBSIEST #IRELIM #REGNIEEC </p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, IT Product Management – Source to Pay]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45507]]></requisitionid>
    <referencenumber><![CDATA[R45507]]></referencenumber>
    <apijobid><![CDATA[r45507]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45507/associate-director-it-product-management-source-to-pay/]]></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>As an Associate Director, IT Product Management – Source to Pay, you will lead the IT execution, delivery, and operational ownership of Regeneron’s Source-to-Pay (S2P) capabilities within a modern, global ecosystem. This role is accountable for translating product strategy and roadmap direction into high-quality, scalable, and compliant solutions that support Global Procurement, Finance, and Supply Chain operations.</p><p>Success in this role requires not only deep Oracle EBS and Fusion S2P expertise, but also deep Procurement industry knowledge.</p><div></div><p>A typical day in this role might look like:</p><ul><li>Serve as IT Product Owner for Oracle EBS and Fusion Cloud Source-to-Pay and associated boundary systems, including but not limited to Procurement (Direct and Indirect), Purchasing, Sourcing/eRFx, Supplier Portal, Supplier Qualification Management, Third Party Risk Management initiatives and Accounts Payable</li><li>Be a Strategic and trusted IT Partner to business to understand Global Procurement, AP, and Supplier (including ASL and Qualification Management) needs in support of the digital strategy, corporate objectives, and functional priorities.</li><li>Drive S2P end-to-end process, supplier master data and governance (along with Supply Chain) and technology deliverables supporting global growth including standardization.</li><li>Lead IT deliverables for multi-year Procurement Technology Transformation Roadmap and Strategy, deliver on Business outcomes</li><li>Partnering strategically with business for Vendor Selections, RFPs, Cost benefit analysis, application rationalization on an ongoing basis.</li><li>Prepare and maintain project and day-to-day business requirements, functional and system designs, solution documentation, and test plans.</li><li>Provide oversight of system integrators and vendors, ensuring delivery aligns with enterprise standards, Oracle best practices, and future‑state architecture.</li><li>Execute and enforce application, integration, and data architecture standards.</li><li>Partner with technical leads on integrations and extensions involving OIC, APIs, file-based integrations, and data exchanges with upstream and downstream systems.</li><li>Provide techno-functional ownership and oversight for procurement-related boundary systems including Icertis (contract management), ORO (procurement orchestration), Sievo (spend analytics), and Trustpair (supplier bank validations)</li><li>Lead participation in Integration Testing, SIT, UAT, regression testing, and quarterly Oracle patch impact assessments for all P2P-related functionality.</li><li>Maintain strong Identity and Access Management controls (RBAC / ABAC) across sensitive procurement and financial systems.</li><li>Partner with Infosec and other technology teams to ensure alignment with Regeneron security standards and ensure compliance on ERP platforms, SaaS, and third-party applications for patching, data security, privacy.</li></ul><p>This role might be for you if you have:</p><ul><li>Proven experience delivering global S2P implementations, ERP modernizations, or complex rollouts.</li><li>Experience across Oracle ERP Procurement, Finance, and Supply Chain applications</li><li>Deep experience with Direct Procurement and Supplier Onboarding specifically related to complex ASL and Supplier Qualification process</li><li>Oracle Fusion Cloud Procure-to-Pay process areas.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in a related field (Business, Finance, Supply Chain, Information Systems) and 10+ years of experience across Oracle ERP Procurement, Finance, and Supply Chain applications with deep experience with Direct Procurement and Supplier Onboarding specifically related to complex ASL and Supplier Qualification process plus 4+ years of hands-on experience with Oracle Fusion Cloud Procure-to-Pay process areas.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Scientist, Genetics Medicine]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43434]]></requisitionid>
    <referencenumber><![CDATA[R43434]]></referencenumber>
    <apijobid><![CDATA[r43434]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43434/senior-manager-clinical-scientist-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>We are seeking a Senior Manager to join our Clinical Sciences team within Regeneron Genetics Medicine. Qualified scientist with training in the pharmaceutical/biotechnology sector, or academic or clinical setting. You will work closely with supervisor and other members of the cross-functional team, contributes to early development and clinical experimentation for projects for discovery phase through Proof of Concept (POC). </p><p>As a Senior Manager, a typical day may include the following:</p><p><br>- Supports the cross-functional study team on the following activities, including but not limited to: </p><p>- Contributes to the writing of sections of Clinical Study Concepts (CSCs) and Clinical Study Protocols (CSPs) and amendments.</p><p>- Assists with identifying key internal and external collaborators/advisors, organizes consultations with global subject matter experts</p><p>- Represents the clinical genetics medicine function on clinical study teams, contributing medical/scientific knowledge to timely and compliant clinical trial execution and quality of deliverables</p><p>- Works alongside Clinical Trial Manager to provide day-to-day clinical input to the study team</p><p>- Drafts portions of the clinical sections in regulatory and clinical documents such as: regulatory agency briefing books, IND/IMPD submissions, investigator’s brochure, informed consent forms, IRB/IEC submissions, clinical study reports, abstracts/manuscripts for publication, etc.</p><p>- Reviews study related documents such as: medical monitoring plans, statistical analysis plans, data management plan, eCRF completion guidelines, data validation manuals, database UAT, etc</p><p>- Trains and support study team and CRO personnel regarding clinical aspects of trial</p><p>- Assist with medical monitoring, raising and responding to investigator queries, writing safety narratives, analysis of trends of safety and efficacy, etc.</p><p>- Organizes steering committees, advisory boards, and data safety monitoring boards as required</p><p>- Identifies program, trial or data risks, creates and implements mitigation strategies</p><p>- Ensures Clinical Team compliance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety.</p><p>- Provides background literature searches in support of:</p><p>- Early clinical strategy in terms of indication selection, study rationale, scientific/clinical endpoints</p><p>- POC-enabling human studies, First-In-Human (FIH) studies, clinical experimental studies as per clinical strategy</p><p>This role may be for you if:</p><p><br>- Effective communications (verbal & written) and presentation skills are essential</p><p>- Must be able to work productively in a fast-paced collaborative environment</p><p>- Demonstrated/potential for critical thinking skills and sound decision-making</p><p>To be considered for this role, you must have a Bachelor’s degree. Ph.D., PharmD. or Master’s degree in biomedical subject. Additionally, we are seeking 8 years of clinical research/development experience</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 10:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Milwaukee, WI]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45934]]></requisitionid>
    <referencenumber><![CDATA[R45934]]></referencenumber>
    <apijobid><![CDATA[r45934]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45934/medical-specialist-i-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[<p><strong>Geography: Milwaukee, WI</strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with <strong>a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement- Advanced Therapies]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46026]]></requisitionid>
    <referencenumber><![CDATA[R46026]]></referencenumber>
    <apijobid><![CDATA[r46026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>We are looking for a Senior Manager, Global Procurement-Advanced Therapies, with experience in end-to-end procurement strategies/processes and with proven successful global category execution in Contract Development and Manufacturing Operations. Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led for 36 years by physician-scientists, Regeneron's unique ability to translate science repeatedly and consistently into medicine has led to numerous FDA-approved treatments and products in development, almost all of which were homegrown in Regeneron's laboratories.</p><p>A typical day might include the following:</p><ul><li><p>Accountable for supporting the definition and implementation of the global CMO Category strategy to serve global and regional business needs as assigned</p></li><li><p>Works closely with partners to manage discussions related to the CMO Categories and aligns category priorities with Procurement management and business partners</p></li><li><p>Manage negotiations, supplier management activities, and partner engagement activities for the Packaging Category as assigned</p></li><li><p>Takes direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities</p></li><li><p>Supports Global Procurement by participating in organizational decisions in the CMO categories with critical short and long-term impact on the success, efficiency, growth, and results of the category team</p></li><li><p>Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities</p></li></ul><p>The Role Might be for you if have:</p><ul><li><p>Experience leading category activities to ensure compliance with appropriate GxPs and other applicable regulations</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements</p></li><li><p>Managed teams of professional level employees responsible for performing category management tasks (if applicable.)</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li><li><p>Working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li></ul><p>We are looking for someone with a bachelor's degree in a relevant field of study plus relevant, progressive experience in procurement, including experience in Pharma/BioPharma or science in general.</p><ul><li><p>Sr Manager level: 8+ years of experience in relevant functions or industries, demonstrating growth in experience, scale, and development throughout.</p></li></ul><p>*This role requires working onsite 5 days per week</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>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Cleanroom Specialist]]></title>
    <date><![CDATA[Sun, 21 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43902]]></requisitionid>
    <referencenumber><![CDATA[R43902]]></referencenumber>
    <apijobid><![CDATA[r43902]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43902/cleanroom-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>We are currently looking to add a Cleanroom & HEPA Certification Specialist to our growing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Cleanroom & HEPA Certification Specialist will support our manufacturing by coordinating the performance of preventive maintenance and on-demand work of certification activities.</p><div><p>As a Cleanroom & HEPA Certification Specialist, a typical day might include the following:</p><ul><li><p>Planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</p></li><li><p>Working with Certification Vendor(s) and Regeneron Facilities, Manufacturing and Lab Management Scheduling Groups to ensure timely certifications of HEPA filtered areas and equipment</p></li><li><p>Recording certification activities in electronic records</p></li><li><p>Ensuring safe and efficient maintenance of all Cleanroom and HEPA supplied equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</p></li><li><p>Being responsible for vendor documentation files, including hardcopy and electronic formats</p></li><li><p>Collecting, trending and analyzing HEPA Filter data</p></li><li><p>Identifying areas for improvement and implementing proactive program enhancements</p></li><li><p>Participating as a Subject Matter Expert (SME) in the creation and revision of Procedures and Work Instructions and supporting Regulatory and Partner Audits as a SME</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Have experience with electronic work record systems (Blue Mountain Regulatory Asset Manager preferred but not required)</p></li><li><p>Have gowning experience for entering and working in Cleanroom environments</p></li><li><p>Have experience in Cleanroom, ISO Classifications, HEPA Filtration or HVAC Systems</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 timelines 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></ul><p>To be considered for the Cleanroom & HEPA Certification Specialist position you must have a BA/BS degree, or equivalent combination of education and experience, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of relevant experience, including experience with CMMS and experience in HEPA Filtration or HVAC Systems, for each level:</p><ul><li><p>Associate 1+ year</p></li><li><p>Specialist: 2+ years</p></li><li><p>Senior Specialist: 5+ years</p></li></ul><p>Prior experience in Cleanroom and HEPA Certification or HVAC preferred.</p><p>Level will be determined based on qualifications relevant to the role.</p></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>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42160]]></requisitionid>
    <referencenumber><![CDATA[R42160]]></referencenumber>
    <apijobid><![CDATA[r42160]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42160/medical-director-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>At Regeneron, we are dedicated to addressing unmet medical needs through groundbreaking therapies. We are seeking a strategic and accomplished <strong>Medical Director, Medical Affairs</strong> to join our team in Tokyo, Japan.</p><p>This role is pivotal in shaping medical strategies and activities for our genetic medicine and rare disease portfolio, with a focus on gene therapy and auditory neuropathy. You will work at the intersection of science, medicine, and innovation, collaborating with internal teams and external stakeholders to ensure scientific excellence and patient-centered outcomes.</p><p>This is a unique opportunity to lead in a cutting-edge field and contribute to therapies that transform lives.</p><br><h3><strong>A Typical Day:</strong></h3><p>As the Medical Director, Medical Affairs, you will:</p><ul><li>Develop and implement medical strategies, including scientific communications, publications, and annual planning.</li><li>Build and maintain partnerships with healthcare professionals, researchers, and advocacy groups to enhance patient care and outcomes.</li><li>Provide medical and scientific leadership to cross-functional teams, ensuring alignment with global and regional strategies.</li><li>Support clinical study sites and regulatory activities, including J-NDA filings and post-approval processes.</li><li>Oversee the generation and dissemination of clinical and non-clinical data to support medical objectives and high-quality publications.</li><li>Organize advisory board meetings to gather insights and inform strategic decisions.</li><li>Ensure scientific accuracy and compliance in medical materials and communications.</li><li>Represent Regeneron Japan in global medical impact teams and external collaborations.</li><li>Attend surgeries or medical procedures to offer technical and scientific guidance when required.</li></ul><br><h3><strong>This Role May Be For You If:</strong></h3><ul><li>You excel in building relationships with diverse stakeholders, including healthcare providers and researchers.</li><li>You thrive in collaborative environments and can align cross-functional teams toward shared goals.</li><li>You possess expertise in translating complex scientific concepts into actionable strategies.</li><li>You are detail-oriented and committed to maintaining high standards of compliance and ethics.</li><li>You have experience in gene therapy and rare diseases, particularly auditory neuropathy.</li><li>You can provide technical and scientific guidance during surgical interventions when required.</li></ul><br><h3><strong>To Be Considered:</strong></h3><p>Candidates must hold an MD or equivalent, with at least 5 years of related industry experience. A strong background in drug development, regenerative medicine, and rare diseases is essential. Fluency in Japanese and English is required, along with the ability to lead technical and business discussions with internal and external stakeholders. Preferred candidates will have experience in gene therapy and auditory disease, as well as a proven track record of medical affairs leadership.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46083]]></requisitionid>
    <referencenumber><![CDATA[R46083]]></referencenumber>
    <apijobid><![CDATA[r46083]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46083/senior-manager-clinical-study-lead/]]></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>SUMMARY/POSITION OBJECTIVE:</strong></p><p>The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global/regional/country execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is 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 out-sourced 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>JOB DUTIES:</strong></p><ul><li><p>Bachelor’s degree and minimum of 8 years relevant industry experience.</p></li><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Provides operational input into protocol development</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Ensures compliance with the clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors </p></li><li><p>Provides input into baseline budget development and management</p></li><li><p>Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level</p></li><li><p>Supports the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Oversees/conducts site evaluation and selection</p></li><li><p>Leads investigator meeting preparation and execution</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</p></li><li><p>Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Ensures accurate budget management and scope changes for internal and external studies</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL)/Country Operations Lead (COL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Oversees the execution of the clinical study against planned timelines, deliverables and budget</p></li><li><p>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</p></li><li><p>Ensure clinical project audit and inspection readiness through the study lifecycle</p></li><li><p>Supports internal audit and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>Contributes to clinical study report writing and review</p></li><li><p>Facilitates and contributes to study level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables</p></li><li><p>Recommends and participates in cross-functional and departmental process improvement initiatives</p></li><li><p>Responsible for identification of innovative approaches to clinical study execution including global considerations 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><li><p>May be responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require 25% travel</p></li></ul><p><strong>JOB REQUIREMENTS:</strong></p><ul><li><p>Exceptional interpersonal & leadership skills</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Advanced communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Strong budget management experience</p></li><li><p>An awareness of relevant industry trends</p></li><li><p>Ability to build, lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Advanced project management skills, cross-functional team leadership and organizational skills</p></li><li><p>Line management experience (Preferred)</p></li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Advanced Informatics Lead]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43335]]></requisitionid>
    <referencenumber><![CDATA[R43335]]></referencenumber>
    <apijobid><![CDATA[r43335]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43335/senior-director-advanced-informatics-lead/]]></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>Regeneron’s growing portfolio is accompanied by ever-increasing amounts of research and clinical data. We are seeking a leader in advanced analytics who can harness the power and insights within our data to improve Global Development (GD), making it more productive while delivering medicines to patients more efficiently and rapidly. Working with a team of data scientists, this position will develop both strategic and technical approaches to improve data access and quality; develop and implement AI/ML algorithms for predictive and descriptive analytics; and advise the GD organization on its overall data strategy. This position will be a key leader in GD’s Digital Transformation (DT) efforts and will work closely with the DT lead to address scientific and informatics challenges. This position will also be a liaison between the DT group and the broader scientific community in GD and all of Regeneron.</p><p><strong>As a Senior Director, a typical day may include:</strong></p><ul><li><p>Establish and implement advanced analytical strategies to extract maximum value from our data. This may include answering clinical questions, using predictive analytics in trial design, automating document analysis and generation, automating development processes, etc.</p></li></ul><ul><li><p>Supervise the development of prototype systems and approaches that, in partnership with IT, can scale to be used on an enterprise level</p></li><li><p>Lead a team of data scientists and developers to create the technical tools and pipelines necessary to implement advanced analytic solutions</p></li><li><p>Drive the development and implementation of cutting-edge analytic solutions, fostering seamless integration and strategic alignment across GD and other Regeneron business units (e.g., Commercial, Research, etc.) to enhance data-driven decision-making and organizational synergy.</p></li><li><p>Collaborate with external partners (vendor, academic, scientific, etc.) to develop and implement relevant solutions</p></li><li><p>Provide scientific and informatics leadership to GD’s digital transformation strategy with an additional focus on organizational change management. Proven ability to lead organizational change, particularly in adopting new technologies and processes, is a plus.</p></li><li><p>Present the advanced analytic strategy to diverse stakeholders across GD and Regeneron and have the ability to influence senior executive leadership and non-technical audiences</p></li><li><p>Develop KPIs to demonstrate the impact of advanced analytic strategies on GD cycle times and other relevant outcomes</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Proven track-record of developing and scaling advanced analytic solutions and advanced analytic strategies and programs in a healthcare or life sciences organization.</p></li><li><p>Demonstrated experience working with large-scale, complex datasets, particularly in the regulated healthcare or clinical trial setting; understanding of clinical data standards is preferred.</p></li><li><p>Demonstrated experience leading teams and overseeing multiple analytical projects, with a focus on guiding the development and implementation of AI/ML solutions.</p></li><li><p>Proven ability to develop and align data strategies that optimize data utilization, support organizational goals, and drive actionable insights.</p></li><li><p>Expertise in Python, R, or other programming languages, with a focus on applying advanced technical skills to data analysis, automation, and software development. Candidates should demonstrate proficiency in writing efficient, scalable, and maintainable code.</p></li><li><p>Proven expertise in evaluating and validating advanced analytic algorithms, ensuring accuracy, reliability, and reproducibility in clinical and research applications. Skilled in developing frameworks for model validation, enhancing data quality, and implementing quality assurance protocols.</p></li><li><p>A research track record with academic publications and/or academic grant support is preferred.</p></li><li><p>Strong analytical and communication skills.</p></li><li><p>May require travel up to 20%.</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>$238,400.00 - $397,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Medicine, Clinical Scientist (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44795]]></requisitionid>
    <referencenumber><![CDATA[R44795]]></referencenumber>
    <apijobid><![CDATA[r44795]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44795/manager-internal-medicine-clinical-scientist-cardio-metabolic-renal/]]></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 Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3>As a Manager in Clinical Sciences, a typical day may include the following:</h3><ul><li>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</li><li>Develops/maintains 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</li><li>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</li><li>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</li><li>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</li><li>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</li><li>Collaborates with internal functions and external vendors to promote clinical study integrity</li><li>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</li><li>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li>Demonstrated ability to influence within team and may influence cross functionally</li><li>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</li><li>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</li><li>Strong management, interpersonal and problem-solving skills</li><li>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements</li><li>Considerable organizational awareness, including significant experience working cross-functionally</li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 5 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in one or more of the following therapeutic areas – cardiovascular, renal, metabolic disease.</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - Dermatology (Charlotte, NC)]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46194]]></requisitionid>
    <referencenumber><![CDATA[R46194]]></referencenumber>
    <apijobid><![CDATA[r46194]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46194/field-reimbursement-manager-dermatology-charlotte-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Charlotte]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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><p><strong>A typical day may include the following:</strong></p><ul><li><p>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.</p></li><li><p>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</p></li><li><p>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).</p></li><li><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p></li><li><p>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</p></li><li><p>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</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</p></li><li><p>You are an ethical, standout colleague and have can grow in a cross-functional team environment - contributing creative ideas and positive energy to the group.</p></li><li><p>You possess excellent organizational, project management, and communication skills.</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p> 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. You have worked with products delivered through a Specialty Pharmacy network is essential. You have the ability to work within an Account Management based structure. You bring knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Allergy - Chicago S, IL]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45932]]></requisitionid>
    <referencenumber><![CDATA[R45932]]></referencenumber>
    <apijobid><![CDATA[r45932]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45932/medical-specialist-i-allergy-chicago-s-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>Our Medical Specialists are at the forefront of engaging Allergists and Immunologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p>As an Allergy Medical Specialist, a typical day might include the following:</p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Global Payroll]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46061]]></requisitionid>
    <referencenumber><![CDATA[R46061]]></referencenumber>
    <apijobid><![CDATA[r46061]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46061/senior-director-global-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 Senior Director, Global Payroll is responsible for leading and transforming payroll operations across the United States, EMEA, and Asia. This role ensures compliance with international labor laws, tax regulations, and data privacy standards while delivering seamless payroll experience for employees in over 10 countries. This person will drive strategic initiatives, manage vendor relationships, and lead a global team to support the company’s growth and operational excellence.</p><p><strong>A typical day in this role might look like: </strong></p><ul><li><p><strong>Develop and execute a global payroll strategy</strong> aligned with organizational goals, workforce expansion, and digital transformation.</p></li><li><p><strong>Serve as a key advisor</strong> to executive leadership on payroll-related risks, compliance, and operational efficiency.</p></li><li><p><strong>Manage payroll processing</strong> for employees across the US, Europe (including UK, Germany, France, Netherlands, etc.), and Asia (including India and Japan).</p></li><li><p><strong>Ensure compliance</strong> with local labor laws, tax codes, social security, and statutory reporting requirements.</p></li><li><p><strong>Oversee expatriate and cross-border payroll complexities</strong>, including shadow payrolls and split payments.</p></li><li><p><strong>Lead and mentor a global payroll team</strong>, including regional directors and country-specific specialists.</p></li><li><p><strong>Manage third-party vendors</strong> (e.g., ADP, BDO, etc.), ensuring SLAs, data integrity, and cost efficiency.</p></li><li><p><strong>Drive talent development</strong> and succession planning within the payroll function.</p></li><li><p><strong>Implement and maintain global payroll systems</strong>, integrating with HRIS (e.g., Workday, Oracle) and finance platforms.</p></li><li><p><strong>Automate workflows</strong> to reduce manual intervention and improve accuracy.</p></li><li><p><strong>Establish KPIs and dashboards</strong> to monitor payroll performance, error rates, and compliance metrics.</p></li><li><p><strong>Ensure adherence to global data privacy laws</strong> (e.g., GDPR, CCPA) and internal audit controls (e.g., SOX).</p></li><li><p><strong>Lead internal and external audits</strong>, responding to inquiries and implementing corrective actions.</p></li></ul><p><strong>This role might be for you if: </strong></p><ul><li><p>Bachelor’s degree in Accounting, Finance, or related field (Master’s preferred).</p></li><li><p>15+ years of progressive payroll leadership experience, including global scope.</p></li><li><p>Proven expertise in managing payroll across US, EMEA, and APAC regions.</p></li><li><p>Strong knowledge of international payroll regulations, tax compliance, and labor laws.</p></li><li><p>Experience with global payroll platforms and integrations.</p></li><li><p>Exceptional leadership, communication, and stakeholder management skills.</p></li><li><p>Certified Payroll Professional (CPP), Global Payroll Management Institute (GPMI), or equivalent.</p></li><li><p>Experience in high-growth, multinational environments (10,000+ employees).</p></li><li><p>Ability to travel internationally as needed.</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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Scientist - Infectious Diseases]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44045]]></requisitionid>
    <referencenumber><![CDATA[R44045]]></referencenumber>
    <apijobid><![CDATA[r44045]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44045/sr-scientist-infectious-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>We are seeking a highly skilled, motivated and innovative <strong>Sr. Scientist</strong> to contribute to antiviral immunological therapies. In this exciting role you will apply your immunology knowledge to progress candidate therapeutic molecules or develop novel immunological strategies to combat viral infections.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li>Drive research projects forward through independently designing, conducting, analyzing <em>in vitro</em> and <em>in vivo</em> experiments and through collaborative involvement </li><li>Perform T cell characterization experiments, such as cytotoxicity assays , T cell activation and cytokine release assays.</li><li>Conduct different viral inhibition assay</li><li>Routinely present findings in a variety of scientific settings within and across departments</li><li>Troubleshooting methodological and technical issues</li><li>Interpreting experimental data and keeping up to date on relevant literature</li></ul><div></div><p><strong>This Role Might Be For You If:</strong></p><ul><li>You enjoy a dynamic, fast-paced environment</li><li>You love to learn, innovate and have a growth mindset</li><li>You are independent and a critical problem solver</li><li>You are resilient in overcoming challenges and expanding areas of expertise</li></ul><p>This role requires a Ph.D. in immunology, infectious disease, virology or related field with a strong publication record. Proven expertise in immunology or infectious disease with experience with in vitro and in vivo experiments is required. The ideal candidate will have deep expertise in immunology and infectious disease experience and be comfortable tackling complex research scenarios.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Advanced Analytics - Immunology]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45943]]></requisitionid>
    <referencenumber><![CDATA[R45943]]></referencenumber>
    <apijobid><![CDATA[r45943]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45943/manager-advanced-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>Regeneron is seeking a Manager, Advanced Analytics, Immunology to join our team!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Manager, Advanced Analytics, Immunology (Nasal Polyps and Eosinophilic Esophagitis) will report into the Director, Immunology (Nasal Polyps and Eosinophilic Esophagitis), within the Commercial Strategy and Insights and Analytics (CSI&A) department. This role will join a high-performing team responsible for overseeing all Advanced Analytics activities for Immunology Nasal Polyps and Eosinophilic Esophagitis and will partner with and serve as a strategic advisor for the Immunology Commercial Business Unit (CBU) stakeholders to inform business decisions.</p><p>The individual will require a strong understanding of how and when to use specific analytical methodologies to drive a high-resolution and up-to-date market understanding, to inform commercial strategy and brand planning.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Manage</em></p><p>1) Assist in shaping the development and implementation of the Nasal Polyps and Eosinophilic Esophagitis BU analytics plan, ensuring alignment with strategic imperatives and business needs.</p><p>2) Oversee performance reporting and analytics, including dashboards, KPIs, and business readouts tied to strategic objectives and definitions of success.</p><p>3) Guide advanced analytics initiatives such as opportunity assessments, predictive modeling, patient finder, next‑best‑action approaches, segmentation, and targeting.</p><p><em>Develop</em></p><p>4) Develop data‑driven insights and analytic approaches that effectively frame and address priority business questions.</p><p>5) Develop robust sub‑national analytics, championing the integration of local market insights into execution and resource optimization.</p><p>6) Develop integrated insights by synthesizing primary and secondary research, market dynamics, competitive trends, and performance analytics.</p><p>7) Proactively identify opportunities through descriptive, prescriptive, and predictive analytics to influence brand strategy, investment decisions, and growth initiatives.</p><p><em>Partnership and collaboration</em></p><p>8) Partner with key Nasal Polyps and Eosinophilic Esophagitis BU stakeholders (Commercial Strategy Insights & Analytics, Marketing, Sales, Access, Finance, Operations, Data Strategy, Incentives & Alignment) to translate insights into action and influence strategic decisions.</p><p>9) Partner with Data Strategy Management to ensure the right datasets are sourced, governed, and leveraged appropriately.</p><p>10) Manage external vendors and analytics partners to ensure analytical deliverables are accurate, actionable, and aligned with business goals.</p><p>11) Collaborate with Market Research teammates to integrate qualitative and quantitative learning into a cohesive narrative.</p><p>12) Ensure compliance with privacy, security, and regulatory requirements across all analytical workstreams.</p><p><em>Support</em></p><p>13) Support sub‑national, HCP, patient, and market opportunity analyses to inform targeting, resource allocation, and field execution strategies.</p><p>14) Assist with ongoing reporting and business review deliverables, including Integrated Business Reviews (IBRs), Quarterly Business Reviews (QBRs), and strategic planning.</p><p>15) Support rigorous analyses using advanced statistical, coding, and BI tools, including SQL, Python/PySpark, R, SAS, Tableau, Qlik, or equivalent.</p><p>16) Measure and track performance against success metrics and business expectations; develop insights that guide course correction.</p><p>17) Support creation of compelling presentations and data stories that communicate complex analytical outputs in a clear, concise, and business‑oriented way.</p><p>18) Contribute to the recommendation of evidence‑based business‑building ideas supported by analytics and integrated insights.</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required; MBA/Master’s degree desired.</p></li><li><p>MBA/Master's degree completed by start date and 3+ years of business analytics, statistics, data mining, applied mathematics, engineering, computer science or related field experience OR Bachelor’s degree and 5+ years of business analytics, statistics, data mining, applied mathematics, engineering, computer science or related field experience: Rhinology, Gastroenterology, Allergy or Immunology experience preferred.</p></li><li><p>Ability to translate complex data into clear business implications for senior leadership.</p></li><li><p>Strong strategic thinking, problem‑solving capability, and analytical rigor.</p></li><li><p>Demonstrated success leading end‑to‑end analytics, performance measurement, and market research integration to influence commercial decisions.</p></li><li><p>Extensive experience with secondary/syndicated datasets (claims, EHR, lab, SP, HUB, distribution, formulary/access, etc.).</p></li><li><p>Hands‑on expertise in SQL, Python/PySpark, R, SAS, or equivalent statistical coding environments.</p></li><li><p>Experience with data visualization and BI tools (Tableau, QlikView, MicroStrategy, Oracle BI, Cognos, Spotfire, etc.).</p></li><li><p>Advanced proficiency in Excel, and PowerPoint required</p></li><li><p>Strong communication, presentation, and storytelling skills with the ability to build rapport and influence across all levels of the organization.</p></li><li><p>Proven success managing multiple complex projects in a fast‑paced environment, delivering high‑quality results under tight timelines.</p></li><li><p>Demonstrated cross‑functional collaboration and the ability to drive alignment across diverse stakeholder groups.</p></li><li><p>Understanding of privacy, regulatory, legal, and compliance frameworks relevant to analytics and data use in biopharma.</p></li><li><p>Prior experience working in an Alliance partnership (preferred)</p></li><li><p>Familiarity with primary research methodologies and the ability to interpret and integrate research findings into analytical framework (preferred)</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs - Hematology - Québec]]></title>
    <date><![CDATA[Fri, 14 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42141]]></requisitionid>
    <referencenumber><![CDATA[R42141]]></referencenumber>
    <apijobid><![CDATA[r42141]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42141/senior-manager-field-medical-affairs-hematology-quebec/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Senior Manager, Field Medical Affairs, Hematology – Québec</strong> </p></div><div><p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p></div><div><p>We are seeking a <strong>Senior Manager, Field Medical Affairs – Hematology</strong> to join our team and strengthen our partnerships with experts in hematologic malignancies. In this role, you will engage with key opinion leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. You’ll play a meaningful role in the understanding of Regeneron’s therapies, supporting clinical development and investigator-initiated research, and contributing to impactful new therapies. </p></div><div><p>We are looking for our next team member to join our passionate & dedicated Medical Affairs team in Canada. This is a remote, field-based role located in the Montreal Area, Quebec, Canada. </p></div><div><p><strong>Senior Manager, Field Medical Affairs, Hematology</strong> </p></div><div><p><strong>Montréal Area, Québec, Canada </strong></p></div><div></div><div><p><strong>A Typical Day:</strong> </p></div><div><ul><li><p>Building and maintaining relationships with KOLs in malignant hematology. </p></li></ul></div><div><ul><li><p>Acting as a primary clinical/scientific contact for HCPs and investigators. </p></li></ul></div><div><ul><li><p>Generating medical insights to advise strategy and development plans. </p></li></ul></div><div><ul><li><p>Supporting clinical trial execution by identifying investigators and trial sites. </p></li></ul></div><div><ul><li><p>Collaborating on abstracts, posters, and manuscripts to communicate data. </p></li></ul></div><div><ul><li><p>Contributing to investigator-initiated study programs and research collaborations. </p></li></ul></div><div><ul><li><p>Attending medical congresses to support scientific exchange. </p></li></ul></div><div><ul><li><p>Partnering cross-functionally with Medical Affairs, Commercial, and Market Access. </p></li></ul></div><div><p><strong>This Role May Be For You:</strong> </p></div><div><ul><li><p>You thrive on scientific exchange and are confident discussing complex data with KOLs. </p></li></ul></div><div><ul><li><p>You have established background in hematology and understand the oncology landscape. </p></li></ul></div><div><ul><li><p>You enjoy balancing independent field work with cross-functional collaboration. </p></li></ul></div><div><ul><li><p>You adapt easily to changing priorities and field-based challenges. </p></li></ul></div><div><ul><li><p>You are motivated by opportunities to contribute to country readiness and new research. </p></li></ul></div></div><div><div><ul><li><p>You value compliance and integrity while working with investigators and partners. </p></li></ul></div><div><ul><li><p>You are comfortable with frequent travel and engaging in high-level conversations. </p></li></ul></div><div><ul><li><p>You are bilingual in English and French Canadian (written/verbal) </p></li></ul></div><div></div><div><p>To be considered, you should bring at least 5 years of field medical or medical manager experience in biotech or pharma, with a strong background in hematology. Knowledge of malignant hematology is required, and experience in lymphoma or multiple myeloma is preferred. Country readiness experience and established KOL relationships are highly valued. You should also have solid knowledge of treatment guidelines, clinical research, and Canadian regulations. Strong communication, organizational skills, and the ability to travel up to 70% are essential. </p></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Tax Planning]]></title>
    <date><![CDATA[Thu, 18 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43986]]></requisitionid>
    <referencenumber><![CDATA[R43986]]></referencenumber>
    <apijobid><![CDATA[r43986]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43986/associate-director-tax-planning/]]></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 Tax Planning role will be responsible for developing, implementing and maintaining tax planning opportunities across Regeneron’s business and supply chain. This is a highly collaborative role, interfacing with leaders and colleagues from all functional areas to optimize Regeneron’s tax positions, in alignment with Regeneron’s evolving business and expanding footprint. This role provides critical leadership and support across all aspects of tax planning including supply chain planning, domestic and international planning and governance, and business development and special projects. This role works closely with internal and external subject matter experts to identify opportunities, execute strategies and document positions. </p><div></div><div><p>The ideal candidate will have the personal drive and enthusiasm to both understand and successfully navigate a fast-growing company in a rapidly evolving marketplace. The ideal candidate will have a hands-on and entrepreneurial style and be willing assist the team and manage projects from development through to finalization. This person is a strategic thinker who approaches challenges with a positive attitude and drives the team towards solutions. This is a visible position with direct contact with Regeneron business leads and senior management. </p></div><p><em><strong>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 work.</strong></em></p><div><p><strong>As an Associate Director, Tax Planning a typical day may include</strong> </p></div><div><ul><li><p>Identify, develop and implement tax planning opportunities in support of Regeneron’s expanding business and supply chain, including modeling financial impact, leading cross-functional assessment and execution, and identifying risk mitigation strategies. </p></li></ul></div><div><ul><li><p>Lead tax aspects of supply chain planning, including optimization of clinical and commercial supply chains, external manufacturing arrangements and distribution models, in alignment with business needs and taking into account domestic and foreign income taxes and indirect taxes. </p></li></ul></div><div><ul><li><p>Research, review and / or draft documentation involving complex tax issues and strategies as may be required in an expanding business, including but not limited to tax technical memoranda, operating manuals, governance policies and reports, and intercompany and third-party agreements. </p></li></ul></div><div><ul><li><p>Support tax efficient international operations and expansion, including optimization of local tax planning and tax incentives, collaborating cross-functional subject matter experts to ensure that finance and business goals are met and reporting is accurate. </p></li></ul></div><div><ul><li><p>Provide end-to-end tax support to Business Development on third-party deals (licenses, collaborations, acquisitions and divestitures and other agreements) including leading diligence to identify risks and opportunities, development of optimal deal structures, review and negotiation of legal documents, and implementation. </p></li></ul></div><div><ul><li><p>Collaborate closely, both internally and externally, with advisors and subject matter experts to ensure tax strategies and implementation contemplate cross-functional impact and are properly documented (including transfer pricing and tax operations). </p></li></ul></div><div><ul><li><p>Monitor U.S. and foreign tax proposals, including OECD BEPS/Pillar Two, working with tax subject matter experts to determine the financial and operational impacts of proposed changes on Regeneron’s tax positions. </p></li></ul></div><div><ul><li><p>Establish strong relationships, demonstrate organizational and interpersonal skills to build a collaborative environment, foster open communication, and educate the business on tax considerations. </p></li></ul></div><div><ul><li><p>Foster a culture of excellence, integrity, and accountability for a growing team. </p></li></ul></div><div><ul><li><p>Interface and interact effectively with personnel at all levels of Regeneron’s organization, including senior leadership, finance leaders, collaborators, external advisors and members of the tax department. </p></li></ul></div><div><div><p><strong>This role may be for you if you have: </strong> </p></div><div><ul><li><p>Mastery of US tax rules, in particular US international tax rules, mergers and acquisitions </p></li></ul></div><div><ul><li><p>Exposure to international supply chain structures, global complexity and foreign tax rules including OECD BEPS and other proposals. </p></li></ul></div></div><div><div><ul><li><p>Ability to research and interpret complex US and non-US tax rules. </p></li></ul></div><div><ul><li><p>Excellent analytical and problem-solving skills required, with the ability to plan and execute at strategic and tactical levels. </p></li></ul></div><div><ul><li><p>Strong communication and interpersonal skills with an ability to effectively relate tax issues to non-tax personnel and upper management. </p></li></ul></div><div><ul><li><p>Strong creative and analytical thought processes, with ability to work in a fast-paced environment with excellent prioritization and organizational skills. </p></li></ul></div><div><ul><li><p>Confident and personable individual, able to work collaboratively inside and outside the tax department and build bridges at all levels of the enterprise. </p></li></ul></div><div><ul><li><p>A superior work ethic, positive attitude, and willingness to jump into projects and assist the team in all areas of tax as may be required at a growing company. </p></li></ul></div><div><ul><li><p>Dedication to the highest work quality and job excellence. </p></li></ul></div><div><ul><li><p>Proficiency with MS Office, in particular, PowerPoint and Excel. </p></li></ul></div></div><p><strong>To be considered for this role you must possess a Bachelor’s degree with 10+ years of experience in tax planning and strategy, including experience in a corporate environment in addition to law firm and/or accounting firm experience. A J.D., CPA or equivalent required, MBA, LLM or Master’s degree in finance a plus.</strong> </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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Drug Supply & Logistics]]></title>
    <date><![CDATA[Tue, 13 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44561]]></requisitionid>
    <referencenumber><![CDATA[R44561]]></referencenumber>
    <apijobid><![CDATA[r44561]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44561/manager-clinical-drug-supply-logistics/]]></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>The <strong>Manager, Clinical Drug Supply & Logistics</strong> is responsible for 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><p><strong>Supply Planning</strong></p><ul><li>Serves as lead drug supply manager for the functional area in supply planning, including demand forecasting according to IOPS requirements.</li><li>Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical development plan.</li><li>Works with clinical drug supply management to determine resourcing needs.</li><li>Provides input to the development of IP-related study documents including protocols, study and pharmacy manuals.</li><li>Responsible for working within established timelines of investigational product manufacturing, labeling, release, distribution and return/destruction, and/or helping to establish these timelines. </li></ul><p><strong>Inventory tracking</strong></p><ul><li>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.</li></ul><p><strong>Shipments</strong></p><ul><li>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.</li></ul><p><strong>IVRS</strong></p><ul><li>Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS.</li><li>Works with cross-functional teams to develop specifications and support user testing of IRT systems provided by 3rd party vendors.</li><li>Leads effort for clinical supply management functionality.</li><li>Monitors and manages clinical supply activities through IRT from study start-up through study closure.</li></ul><p><strong>Returns & Destruction</strong></p><ul><li>Develops strategy and oversees drug return and destruction activities.</li></ul><p><strong>Expiry Management</strong></p><ul><li>Develops resupply strategies based on stability and shelf-life of clinical supplies.</li><li>Monitors IP expiry data and informs Clinical Supply team and Clinical Trial teams of pending IP expiry.</li></ul><p><strong>Ancillary & Comparator Supplies</strong></p><ul><li>Coordinates with other functional areas, including Regulatory, Medical Director, Forecasting & Planning, and IOPS to define ancillary and/or comparator supply strategy.</li><li>Develops plans for supplying clinical study sites with ancillary and/or comparator supplies, either through in-house initiated supply or working with supply vendors.</li></ul><p><strong>Documentation</strong></p><ul><li>Provides input to drug kit randomization specifications and reviews and approves master kit lists</li><li>Designs, reviews and approves IP-related study tools (for clinical study teams and investigative site use), as needed.</li><li>Supports inspection team in preparation for and during regulatory agency inspection.</li></ul><p><strong>Study Team Interaction</strong></p><ul><li>Represents Clinical Drug Supply & Logistics on cross-functional study team (s) and/or sub-team(s).</li><li>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.</li></ul><p><strong>Budget Management</strong></p><ul><li>Provides input into budgets, SoWs, contracts and timelines for IP-related services.</li><li>Creates RFPs, reviews quotes, and awards third-party vendors for distribution services.</li><li>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.</li></ul><p><strong>Vendor Management</strong></p><ul><li>Leads management of IP service vendors (performance, quality, timelines, deliverables, costs)</li><li>Participates in preparation of RFP, assumptions and SOW for CROs and IP services vendors (labeling, packaging, distribution; IVRS/IWRS)</li><li>Provides input, reviews, and approves vendor study specifications for IP-related activities.</li><li>Serves as point of escalation for vendor-related IP issues as they arise.</li><li>May require 25% travel</li></ul><p><strong>Staff Management</strong></p><ul><li>Does not supervise staff.</li><li>May mentor or coach junior Clinical Drug Supply& Logistics staff.</li></ul><p><strong>Process Initiatives</strong></p><ul><li>Develops and implements process initiatives in accordance with business needs.</li></ul><p><strong>Metrics</strong></p><ul><li>Tracks metrics related to drug supply processes and staff.</li></ul><p><strong>Training</strong></p><ul><li>Provides assistance in training and development as needed.</li></ul><p><strong>Reporting</strong></p><ul><li>Compiles and reports supply status to study teams and senior management</li></ul><p><strong>Problem solving</strong></p><ul><li>Applies knowledge of company policies and standard practices to resolve problems.</li></ul><p><strong>In order to be considered for this role,</strong> a minimum of bachelor's degree and at least 6 years of relevant experience in the biotechnology/pharmaceutical industry, with 3 years minimum in clinical supply management. A Masters/MBA/PharmD with 3+ years of relevant industry experience is preferred</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 14 Jan 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff IT Compliance Analyst]]></title>
    <date><![CDATA[Tue, 20 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43076]]></requisitionid>
    <referencenumber><![CDATA[R43076]]></referencenumber>
    <apijobid><![CDATA[r43076]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43076/staff-it-compliance-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Staff IT Compliance Analyst plays a critical role in ensuring that the Manufacturing IT group operates in full compliance with regulatory requirements, industry standards, and Regeneron’s internal quality procedures. This role also oversees the preparation and management of internal and external audits to maintain a state of inspection readiness.</p><p>As a Staff IT Compliance Analyst, a typical day might include the following:</p><ul><li>Providing expert guidance and analysis to the Manufacturing IT team on regulatory compliance, quality assurance, and inspection readiness, while managing internal programs to ensure audit preparedness.</li><li>Evaluating, developing, and refining Manufacturing IT policies, standard operating procedures (SOPs), and practices to align with regulatory requirements, corporate quality standards, and industry best practices.</li><li>Representing and supporting Manufacturing IT subject matter experts (SMEs) during internal and external audits, while leading the development and execution of responses to audit findings.</li><li>Establishing, maintaining, and improving metrics to monitor IT compliance, inspection readiness, and audit outcomes, and effectively communicating these findings to stakeholders.</li><li>Collaborating with global sites to ensure deployed systems comply with business needs, regulatory expectations, and data integrity requirements, while promoting a culture of quality and continuous improvement.</li><li>Monitoring industry trends in audit observations and regulatory changes, identifying potential compliance gaps, and implementing timely corrective or preventive actions.</li><li>Supporting IT quality processes, including managing IT deviations, change controls, and the creation or revision of IT quality documents, while demonstrating flexibility and cross-functional expertise.</li></ul><p>This role may be for you if you have:</p><ul><li>A deep understanding of GxP regulations (e.g., FDA 21 CFR Part 11, EU Annex 11) and expertise in IT system validation and qualification processes.</li><li>Proven ability to apply quality assurance principles to IT compliance activities, ensuring systems and processes meet both regulatory and corporate quality standards.</li><li>Strong analytical and problem-solving skills, with a proactive approach to identifying and resolving compliance risks.</li><li>Excellent communication and collaboration skills to work effectively across global teams and interact with regulatory inspectors or auditors.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field required along with</p><ul><li>Principal IT Compliance Analyst: 8 years of relevant experience.</li><li>Staff IT Compliance Analyst: 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>Quality Assurance (QA) experience strongly desired.</li><li>Experience in the pharmaceutical or biotechnology industry preferred.</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 21 Jan 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology- Virginia Beach, VA]]></title>
    <date><![CDATA[Mon, 02 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45016]]></requisitionid>
    <referencenumber><![CDATA[R45016]]></referencenumber>
    <apijobid><![CDATA[r45016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45016/medical-specialist-i-dermatology-virginia-beach-va/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Virginia Beach]]></city>
    <state><![CDATA[Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: </strong>Virginia Beach, VA<br>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>As a Medical Specialist, a typical day may include the following:</strong><br>• Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area<br>• Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups<br>• Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs<br>• Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives<br>• Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p><p><strong>This role may be for you if:</strong><br>• You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals<br>• You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values<br>• You have a competitive spirit and harness your “grit” to power your approach to sales<br>• You collaborate effectively with internal and external partners<br>• You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends<br>• You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.<br>#derm<br><br> </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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Feb 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - Neurology]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44952]]></requisitionid>
    <referencenumber><![CDATA[R44952]]></referencenumber>
    <apijobid><![CDATA[r44952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44952/director-global-patient-safety-sciences-neurology/]]></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>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><div><div><div><div><div><p><strong>In this role, a typical day might include:</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></ul><p><strong>This role might be for you if can/have:</strong></p><ul><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>To be considered for this opportunity, you must have the following:</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></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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 13:26:34 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Tue, 03 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44964]]></requisitionid>
    <referencenumber><![CDATA[R44964]]></referencenumber>
    <apijobid><![CDATA[r44964]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44964/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[<div><div>The Medical Director, Clinical Sciences should be a qualified physician with pharmaceutical industry experience, preferably in Ophthalmology Therapeutics Development. The Director will serve as Medical Lead for clinical trials in the CDP and is responsible for the design of clinical study concepts leading to clinical trial protocols. 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.</div></div><div><div><div><div><p><strong>A typical day in the life of a Medical Director may include the following responsibilities:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external stakeholders</p></li><li><p>Defines clinical trial-related Clinical Development Program (CDP) goals and objectives </p></li><li><p>Works closely with discovery teams to provide input on the next generation of targets in the field</p></li><li><p>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts </p></li><li><p>Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings</p></li><li><p>Leads the Global Clinical Study Team to produce high quality program deliverables on schedule </p></li><li><p>Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety </p></li></ul><p><strong>This job may be for you if you have the following: </strong></p><ul><li><p>M.D. or equivalent with board eligibility or board certification in Ophthalmology, Rheumatology, Neurology, or Immunology</p></li><li><p>0-4 years pharmaceutical industry experience (equivalent research in academia will be considered)</p></li><li><p>Experience in Ophthalmic 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>#MDJOBS, #MDJOBSCD#GDTherapeuticJobs</p></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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Feb 2026 12:26:28 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Richmond, VA]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45017]]></requisitionid>
    <referencenumber><![CDATA[R45017]]></referencenumber>
    <apijobid><![CDATA[r45017]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45017/medical-specialist-i-dermatology-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</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Precision Medicine]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44954]]></requisitionid>
    <referencenumber><![CDATA[R44954]]></referencenumber>
    <apijobid><![CDATA[r44954]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>The Precision Medicine group at Regeneron is responsible for designing, implementing, executing, analyzing and interpreting the overarching clinical biomarker strategies for therapeutic candidates during clinical development. We are seeking to hire a hands-on Precision Medicine Strategy Lead (PMSL) roles at the director level, with backgrounds in one or more therapeutic areas within the group. We are seeking someone to independently oversee the development and execution of biomarker strategies across one (or more) therapeutic areas depending on their areas of expertise, with a preference in obesity / metabolism pharmaceutical development.. The following therapeutic areas are in scope: Neurodegenerative Disorders, Cardiovascular Disease, Muscle and Metabolism Disorders, and/or Rare Genetic Diseases). In this highly matrixed role, they will design, develop, communicate at senior levels and operationally implement clinical biomarker strategies to support key programs in early and late stage drug development. Clinical technologies applied include biomarker assays, pharmacogenetic assessments, as well as other clinical and physiological testing devices. </p><p><strong>A typical day may include:</strong></p><ul><li><p>Enhancing our understanding of indications at a cellular and molecular level</p></li><li><p>Conducting novel biomarker discovery, qualifying new biomarkers/approaches to expedite proof-of-concept for new drug candidates.</p></li><li><p>Optimizing label claims for later stage candidates, enabling personalized medicine principles to be applied, as appropriate, in full development. </p></li><li><p>With a focus in therapeutic areas outside of Oncology, broad understanding of disparate biomarker technologies, and deep experience in biomarker assay development and validation in clinical drug development </p></li><li><p>Responsible for conducting in-depth literature and technology reviews pertinent to assigned clinical development programs within the TFA, identifying and pulling in experts in multiple disease areas, navigating and supporting the logistical and regulatory factors pertaining to clinical technologies.</p></li></ul><p><strong>This role may be for you if have experience with the following:</strong></p><ul><li><p>TA--level lead for implementation of strategic vision for clinical biomarkers in one or more therapeutic areas across multiple programs with multiple studies that will broadly enable advances in target identification, indication selection, early indication of biological activity and patient stratification/selection</p></li><li><p>Serve as an individual contributor and senior-level representative of Precision Medicine on development teams and deliver biomarker strategies to key programs from initial concept to execution, data delivery and results interpretation</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine and clinical biomarker strategies for molecules in discovery phases (leading to candidate molecule selection)</p></li><li><p>Represent Regeneron and work with colleagues from allied companies to develop and implement strategies for partnered alliances</p></li><li><p>Collaborate with clinical operations teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Design, oversee and manage internal and external research collaborations in areas of clinical technologies and translational research</p></li><li><p> Accountability for ensuring complex clinical assays used in programs in the TFA portfolio of clinical development are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with internal Regeneron laboratories (e.g. Discovery Research, Molecular Profiling, Regeneron Genetics Center, DNA core, BioAnalysis, etc.) to develop plan for validation and application of research assays</p></li><li><p>Ensure timely delivery of results across selected programs, consistent with program team and senior management expectations in a way that increases the potential impact of Precision Medicine deliverables on Global Development programs</p></li><li><p> Contribute to and ensure the quality of Precision Medicine technical reports, study memos and clinical study reports, data reviews and interpretations, scientific publications and recommendations to development teams and management.</p></li></ul><p><strong>To be considered for this role</strong>, you must have a PhD and 10+ years of experience driving, managing, executing and delivering results for complex multi-functional projects. You have excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills. Strong track record in mentorship and development of direct reports.</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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 21:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director CMC Regulatory Affairs]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45198]]></requisitionid>
    <referencenumber><![CDATA[R45198]]></referencenumber>
    <apijobid><![CDATA[r45198]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45198/associate-director-cmc-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, CMC Regulatory Affairs provides leadership for an assigned product portfolio with a focus on ex-US markets. In this role, you will be responsible for the development and execution of global regulatory strategies for combination products and medical devices, mentor Regulatory Affairs staff, support cross-functional program teams and development partners, and lead ex-US Health Authority activities. This position is ideal for a regulatory leader who thrives in a matrixed, international environment and partners closely across programs and regions to bring therapies and devices to patients worldwide.</p><p><strong>A Typical Day</strong></p><ul><li>Lead combination product and device global development activities from early phase through submissions and post-market requirements, incorporating input from senior management.</li><li>Represent Combination Products Regulatory Affairs (CP RA) at program meetings and independently provide regulatory interpretation, positions, and strategy for global CP portfolios across initial registrations and post-approval activities.</li><li>Proactively identify program issues and develop regulatory strategies to mitigate risks to filings; find alternative solutions/workarounds and secure interpersonal consensus.</li><li>Critically review and provide strategic feedback on regulatory documents (e.g., IMPDs, meeting packages, scientific advice, MAAs, quality defect assessments, Notified Body Opinions) to expedite development, licensure, and market access.</li><li>Lead and facilitate interactions with global regulatory authorities (e.g., meetings, responses to information requests, inspections).</li><li>Perform review and approval of compliance activities to confirm regulatory impact and device submission requirements for clinical and commercial filings; mentor colleagues through compliance assessments and identify process improvements.</li><li>Present CP RA perspectives at internal and external forums (e.g., department meetings, conferences, workshops).</li><li>Participate in company working groups and build cross-functional collaboration.</li><li>Develop Working Instructions, SOPs, and Reviewer’s Guides to promote consistent, efficient practice across CP RA units.</li><li>Identify regulatory gaps in manufacturing and global RA processes, advance appropriately, and contribute to business efficiency improvements.</li><li>Establish, lead, and maintain a knowledge base of current and emerging CP regulatory guidelines.</li><li>See opportunities to initiate operational changes and policy modifications.</li><li>Act as a mentor and coach for team members.</li></ul><p><strong>This Role Might Be for You If You Have</strong></p><ul><li>Experience supporting combination products through development and approval.</li><li>Strong understanding of global CP RA regulations, with particular focus on EU Medical Device Regulation 2017/745.</li><li>Experience engaging with EMA and EU Notified Bodies.</li><li>Experience with device regulatory requirements and development processes for combination products, including authoring technical documents (e.g., test reports, technical memos, input requirements, human factors protocols).</li><li>Experience preparing information for CE mark and Notified Body Opinion submissions.</li><li>Critical thinking, strong problem-solving, and risk mitigation skills.</li><li>Excellent communication, negotiation, and presentation abilities.</li><li>Consistent track record in building collaboration and partnership across cross-functional teams.</li></ul><p><strong>To be considered, </strong>you bring a bachelor’s degree in a relevant technical or scientific field (advanced degree strongly preferred), a minimum of 10 years of pharmaceutical/biotech or equivalent regulatory experience, and at least 5 years of relevant CMC/device experience. You are willing and able to travel internationally as needed to support regulatory meetings, inspections, and stakeholder engagements.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Feb 2026 02:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Savannah, Ga / Charleston, SC]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45032]]></requisitionid>
    <referencenumber><![CDATA[R45032]]></referencenumber>
    <apijobid><![CDATA[r45032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45032/medical-specialist-i-dermatology-savannah-ga-charleston-sc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Savannah]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Savannah, Ga / Charleston, SC</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Country Medical Director (f/m/d), Germany]]></title>
    <date><![CDATA[Sat, 14 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44908]]></requisitionid>
    <referencenumber><![CDATA[R44908]]></referencenumber>
    <apijobid><![CDATA[r44908]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44908/country-medical-director-fmd-germany/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Als Country Medical Director (w/m/d) vertrittst du Regeneron in Deutschland über alle Aktivitäten der Medical Affairs und der Klinischen Entwicklung hinweg. Du fungierst als zentrale medizinische und wissenschaftliche Ansprechperson im Land, verantwortest die Ausgestaltung der nationalen medizinischen Strategie und stellst die enge Abstimmung mit globalen Vorgaben sicher. In einer hochgradig kollaborativen, funktionsübergreifenden Matrix arbeitest du mit internationalen Teams zusammen, stärkst Regenerons wissenschaftliche Präsenz in Deutschland und treibst medizinische Exzellenz voran.</p><p><strong>Ein typischer Arbeitstag kann folgende Tätigkeiten umfassen:</strong></p><ul><li><p>Vertretung von Regeneron in Deutschland als zentrale medizinische Ansprechperson für interne Stakeholder (Medical Affairs, Clinical Development, Operations, Regulatory, Commercial) sowie externe Partner (medizinische Fachgesellschaften, wissenschaftliche Einrichtungen, Key Opinion Leaders).</p></li><li><p>Repräsentation der Medical Affairs in funktionsübergreifenden Meetings und enge Zusammenarbeit mit globalen Therapeutic Area Medical Directors sowie Teams wie HEOR, Medical Education und Medical Information zur Optimierung der strategischen und operativen Planung.</p></li><li><p>Medizinische Leitung für klinische Entwicklungsaktivitäten in Deutschland, einschließlich Identifikation von Centers of Excellence und relevanten Prüfzentren; Unterstützung von Investigator Meetings und Rekrutierungsstrategien.</p></li><li><p>Kontinuierliche Pflege fundierter wissenschaftlicher und klinischer Expertise in Onkologie/Hämatologie sowie Verständnis der klinischen Entscheidungswege und Patient Journeys.</p></li><li><p>Wissenschaftlicher Austausch mit externen Expert:innen zur Förderung des Verständnisses und der sachgerechten Anwendung von Regeneron‑Arzneimitteln.</p></li><li><p>Einbringen der Perspektive deutscher Patient:innen und Ärzt:innen in funktionsübergreifende strategische Diskussionen – unter Berücksichtigung wissenschaftlicher, klinischer und ökonomischer Aspekte.</p></li><li><p>Teilnahme an wissenschaftlichen Kongressen, Symposien und Advisory Boards; Unterstützung bei der Entwicklung und Lokalisierung wissenschaftlicher Inhalte.</p></li><li><p>Durchführung wissenschaftlicher Präsentationen für verschiedene Zielgruppen wie Ärzt:innen, Apotheker:innen, Kostenträger und interne Teams.</p></li><li><p>Medizinische Unterstützung lokaler Clinical‑Operations‑Aktivitäten sowie Sicherstellung der engen Abstimmung mit der Unternehmenszentrale.</p></li><li><p>Analyse der medizinischen Weiterbildungsbedarfe und Ableitung entsprechender interner und externer Strategien.</p></li><li><p>Beitrag medizinischer Expertise zu kommerziellen Strategien, z. B. Launch‑Vorbereitung, Market Access und Life‑Cycle‑Management.</p></li><li><p>Sicherstellung der regelkonformen Prüfung und Freigabe wissenschaftlicher und werblicher Materialien gemäß geltender gesetzlicher Vorgaben und interner Richtlinien.</p></li></ul><p><strong>Diese Rolle passt zu dir, wenn du Folgendes mitbringst:</strong></p><ul><li><p>Ein abgeschlossenes Medizinstudium (bevorzugt Promotion/approbierte:r Arzt/Ärztin) oder eine gleichwertige Qualifikation mit nachweislicher Expertise in Onkologie/Hämatologie; klinische Erfahrung ist von Vorteil.</p></li><li><p>Mindestens 15 Jahre kombinierte Berufserfahrung im klinischen Setting sowie in der pharmazeutischen/biopharmazeutischen Industrie, überwiegend in leitenden Medical Affairs‑Funktionen.</p></li><li><p>Erfahrung in der Leitung von Office‑ und Field‑Based‑Medical‑Teams inkl. Führung über unterschiedliche Ebenen hinweg.</p></li><li><p>Tiefes Verständnis des deutschen Gesundheitssystems, der regulatorischen Rahmenbedingungen und der Prozesse der Arzneimittelentwicklung.</p></li><li><p>Nachweisliche Fähigkeit, in einer komplexen, funktionsübergreifenden Matrix zu arbeiten und strategische medizinische Pläne voranzutreiben.</p></li><li><p>Hervorragende medizinisch‑wissenschaftliche Kommunikationsfähigkeiten sowie die Fähigkeit, präzise und handlungsrelevante Empfehlungen abzuleiten.</p></li><li><p>Erfahrung in der Zusammenarbeit mit internen Stakeholdern und externen Expert:innen sowie ausgeprägte Netzwerk‑ und Beziehungskompetenz.</p></li><li><p>Hohe wissenschaftliche Integrität, Zuverlässigkeit und Umsetzungsstärke.</p></li><li><p>Ausgeprägtes strategisches Denken, Stakeholder‑Management‑Fähigkeiten und die Fähigkeit, komplexe medizinische Inhalte verständlich darzustellen.</p></li><li><p>Proaktives, unternehmerisches Mindset, Belastbarkeit und die Fähigkeit, mehrere Prioritäten gleichzeitig zu managen.</p></li><li><p>Verhandlungssichere Deutsch‑ und Englischkenntnisse.</p></li><li><p>Reisebereitschaft von ca. 30–50%.</p></li></ul><p><strong>Darüber hinaus hast du:</strong></p><ul><li><p>Umfassende Führungserfahrung in verschiedenen Bereichen der Medical Affairs, einschließlich Second‑Line‑Leadership.</p></li><li><p>Expertise in strategischer Planung, Launch‑Vorbereitung, Zusammenarbeit im Bereich Market Access und Medical Governance.</p></li><li><p>Sehr gute Kommunikations‑, Verhandlungs‑ und Analysefähigkeiten.</p></li><li><p>Die Fähigkeit, eigenständig zu arbeiten, fundierte Entscheidungen zu treffen und in einem dynamischen Umfeld effektiv zu agieren.</p></li></ul><p>Sehen Sie sich selbst in dieser Stellenbeschreibung? Dann bewerben Sie sich jetzt und machen Sie den ersten Schritt in Richtung „Regeneron Way“! Wir haben eine inklusive Kultur, die umfangreiche Sozialleistungen bietet, die je nach Standort variieren. In den USA können die Leistungen Gesundheits- und Wellnessprogramme (einschließlich Krankenversicherung, Zahn-, Sehkraft-, Lebens- und Berufsunfähigkeitsversicherung), 401(k)-Zusatz des Unternehmens, Familienleistungen, Aktienzuteilung, bezahlte Freistellungen und bezahlten Urlaub (z. B. Militär- und Elternzeit), für berechtigte Mitarbeiter auf allen Ebenen umfassen! Für weitere Informationen über die Leistungen von Regeneron in den USA siehe https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. Für die spezifischen Vorteile anderer Länder sprechen Sie bitte mit Ihrem Personalberater.<br>Wir sind der Meinung, dass wir bei Regeneron am erfolgreichsten sind und am besten arbeiten, wenn wir zusammen sind. Aus diesem Grund sind viele Aufgaben bei Regeneron nur vor Ort zu erfüllen. Bitte wenden Sie sich an Ihren Personalberater und Personalverantwortlichen, um weitere Informationen über die Vor-Ort-Richtlinien von Regeneron und über die Erwartungen für Ihre Rolle und Ihren Standort zu erhalten.<br> </p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 14 Feb 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Program Operations Leader, Oncology]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45269]]></requisitionid>
    <referencenumber><![CDATA[R45269]]></referencenumber>
    <apijobid><![CDATA[r45269]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45269/director-program-operations-leader-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>The <strong>Director Program Operations Leader</strong> (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><strong>Director Program Operations Leader - Oncology </strong></p><p><em>(For US Locations, this position is on-site 4 days per week and 1 day from home. For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days from home. A fully remote role is NOT possible for this position.)</em></p><p><strong>In a typical day, you will:</strong></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><strong>To be considered, you must possess</strong> 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><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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager,   GCP Quality Management- Global Development]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44852]]></requisitionid>
    <referencenumber><![CDATA[R44852]]></referencenumber>
    <apijobid><![CDATA[r44852]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44852/senior-manager-gcp-quality-management-global-development/]]></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>The Senior Manager, Global Development Quality Management (GCP) acting as a Quality Management Lead (QML) is a key position that will provide guidance and leadership for all aspects of quality and compliance within Global Development Quality (GDQ) systems. The GDQM (GCP) QML will engage with key stakeholders, build strategic partnerships working and liaising with study teams, relevant functions and other GDQ functions to lead risk-based quality management activities on all Regeneron-sponsored clinical trials, inclusive of issue management and providing continuous support of inspection readiness.</p><p>For US locations (Armonk, NY or Warren, NJ), this role is on-site 4 days in the office and 1 day from home. For Uxbridge, UK or Dublin, Ireland this role would be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position.</p><p><strong>A day in the life may look like:</strong></p><p>• Acting as a Subject Matter Expert (SME) and key liaison to GDQ to provide support and advise on any quality issues to ensure compliance and for the Quality Risk Assessment process.<br>• Ensuring and responsible for Risk-Based Quality Management (RBQM) initiatives and process improvements, in partnership with other functional areas.<br>• Responsible for the management of GCP-compliant activities from a quality perspective in conjunction with the business and the GDQM (GCP) team.<br>• Providing day-to-day quality and compliance support to cross-functional stakeholders, including issue management (triage/investigation/actions), audit responses, proactive quality management, Corrective Action/Preventive Action (CAPA) oversight, audit/issue trending.<br>• Engaging with, supporting, and liaising with multiple cross-functional stakeholders whose work impacts the GDQ system.<br>• Leading Quality Risk Assessment and Control Tracker (QRACT) activities at the time of Protocol development predicated on ICHGCP.</p><p><strong>This may be the right role for you if you have experience:</strong></p><p><strong>•</strong> Bachelor's degree with a minimum of 8 years of relevant healthcare/pharmaceutical industry experience.<br>• Experience working in either a quality/compliance role (e.g., Quality Management, Quality Assurance etc.), or in a Clinical Development role with expertise and/or transferable skills related to Good Clinical Practice (GCP), and/or Good Pharmacovigilance Practice (GVP).<br>• Providing consultation, mentorship, training, and support in respect to compliance with applicable international regulations, practices, and guidelines.<br>• Advising on the escalation of any quality issues that potentially represent serious non-compliances (or serious breach) via the issue escalation process.<br>• Supporting the collection and reporting of data (e.g., metrics).<br>• Contributing to and supporting process improvement initiatives and workgroups, as assigned.<br>• Exemplifying a quality mindset and behaviors in all interactions with internal and external colleagues, serving as an ambassador for GDQ.<br>In order to be considered for this role, we are looking for candidates who have:<br> </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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Macon, GA]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45031]]></requisitionid>
    <referencenumber><![CDATA[R45031]]></referencenumber>
    <apijobid><![CDATA[r45031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45031/medical-specialist-i-dermatology-macon-ga/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Macon]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Macon, GA</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listen territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[SALES MANAGER – RESPIRATORY　※Chugoku and Shikoku area]]></title>
    <date><![CDATA[Mon, 02 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45705]]></requisitionid>
    <referencenumber><![CDATA[R45705]]></referencenumber>
    <apijobid><![CDATA[r45705]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45705/sales-manager-respiratory-chugoku-and-shikoku-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Summary / Purpose of Position: </strong></p><p>The District Manager collaborates to build and sustain a high-performance team culture aligned with Regeneron's vision, values, and strategic direction. The manager oversees and leads a team of MRs (Medical Representatives) within the assigned region, effectively guiding and managing their performance to achieve sales targets. </p><p><strong>Assigned Area: </strong></p><p>You will be responsible for the Chugoku and Shikoku area. </p><p>Your residence is expected to be in Hiroshima or Okayama.(Hyogo or Osaka also available for consultation)</p><p><strong>Responsibilities: </strong></p><p>Performance Orientation and Leadership: </p><p>- Recruit industry-leading sales representatives (MRs). </p><p>- Conduct training for new employees in collaboration with HR and talent development programs. </p><p>- Manage the performance of MRs in the assigned region by providing appropriate leadership and guidance. </p><p>- Provide targeted and effective feedback, coaching, training, development plans, and talent management for direct reports. </p><p>- Identify best practices and share them across the department. </p><p>- Build effective and productive partnerships with Regeneron's alliance companies. </p><p>- Enhance Regeneron's reputation and expand relationships with key HCPs (Healthcare Professionals). </p><p>Strategic Planning and Effective Execution: </p><p>- Ensure that direct reports acquire high-level knowledge of products, competitive treatments, and market environments to maximize opportunities for Dupilumab market expansion. </p><p>- Provide field input to relevant headquarters departments and assign clear tactical plans to team members, ensuring their execution. </p><p>- Monitor and track key performance indicators to achieve sales and behavioral goals in the assigned region, making adjustments as needed. </p><p>- Manage and allocate resources effectively to ensure sales targets and profitability are achieved. </p><p>- Manage budgets across the assigned region and demonstrate ROI for investments. </p><p>- Ensure agreed-upon advocacy development plans are achieved across the region. </p><p>- Provide performance summaries to relevant business functions (division and HR). </p><p>Regulatory and Corporate Compliance: </p><p>- Fully comply with industry and company procedures. </p><p>- Act in accordance with applicable pharmaceutical industry codes of conduct and Regeneron's SOPs (Standard Operating Procedures). </p><p><strong>Qualifications: </strong></p><p>- Degree or equivalent education in life sciences, pharmacy, chemistry, or biology preferred. </p><p>- Experience in first-line management (field team oversight). </p><p>- Engagement/experience with alliances. </p><p>- Talent management and leadership abilities. </p><p>- Proven track record in account management and sales performance in the pharmaceutical industry. </p><p>- Understanding of financial tools and processes required for brand plan execution. </p><p>- Demonstrated ability to identify opportunities and develop them into business solutions. </p><p>- Strong network, influence, and personal credibility. </p><p>- Ability to plan effectively and prioritize tasks. </p><p>- High-level communication and presentation skills. </p><p>- Excellent commercial insight. </p><p>- Proficiency in IT and digital tools, with the ability to handle data, multiple systems, and CRM. </p><p>- Certification in relevant pharmaceutical industry codes of conduct. </p><p>- Willingness to travel frequently as required by this role. </p><p>- Basic Excel and PowerPoint skills. </p><p><strong>Preferred Qualifications: </strong></p><p>- Knowledge of therapeutic areas (respiratory) and sales experience with biologics. </p><p>- Up-to-date clinical knowledge of therapeutic areas and competitive brands. </p><p>- Network with key opinion leaders in the respiratory field. </p><p>- English proficiency is desirable but not mandatory for this role. </p><p><strong>Minimum Education Requirements: </strong></p><p>- Bachelor’s degree from an accredited university in business, marketing, finance, economics, market research, statistics, social sciences, biological sciences, or physical sciences. </p><p>- At least 7 years of experience in the pharmaceutical industry or related professional experience. </p><p>- Valid driver’s license. </p><p>- MR certification.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Global Lung Cancer Life Cycle Management Lead]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45335]]></requisitionid>
    <referencenumber><![CDATA[R45335]]></referencenumber>
    <apijobid><![CDATA[r45335]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45335/senior-director-global-lung-cancer-life-cycle-management-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><em>This role is on-site in Sleepy Hollow, NY 4 days per week and 1 day from home. Warren, NJ is not a possible location for this role.</em></p><p>The Senior Director, Global Lung 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 Lung Cancer tumor area. The LCM Lead 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 Lung Cancer Marketing. The LCM Lead will collaborate closely with cross-functional teams to support the overall strategic goals of the portfolio and will play a critical role in Commercial/Clinical cross-functional forums.</p><h3><strong>A typical day may include the following:</strong></h3><ul><li>Develop and evolve the global life cycle management strategy (e.g., indication sequencing, geographic expansion) for all in-line oncology assets with Lung Cancer indications to maintain competitive advantage.</li><li>Shape asset plans within Lung Cancer indications in coordination with the Executive Director of Global Lung 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 Lung Cancer Marketing in developing the commercial perspective for Lung 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.</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 Lung 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><p><strong>Budgeting</strong></p><ul><li>Work cross-functionally to create, manage, and track US and global budgets within Lung Cancer, ensuring adherence to approved budgets and phasing.</li></ul><h3>To be considered, you must possess:</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; NMSC 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 and commercial experience in 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 physician-administered (e.g., buy-and-bill) oncology 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 partners 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 customers 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><ul></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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Tue, 24 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44794]]></requisitionid>
    <referencenumber><![CDATA[R44794]]></referencenumber>
    <apijobid><![CDATA[r44794]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44794/manager-clinical-scientist-internal-medicine-cardio-metabolic-renal/]]></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 Manager, Clinical Scientist to join our team. The Manager Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Manager works in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to the Associate Director/Director Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3>As a Manager within Clinical Sciences, a typical day may include the following:</h3><ul><li><p>Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings</p></li><li><p>May contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments</p></li><li><p>Develops/maintains basic 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 limited knowledge of disease and drug landscape</p></li><li><p>Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets</p></li><li><p>May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborate with others for scientific and foundational guidance</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)</p></li><li><p>Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Supports identification of data trends and potential inconsistencies in data across assigned studies and raises</p></li><li><p>Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study</p></li></ul><h3><strong>This role may be for you if: </strong></h3><ul><li><p>Demonstrated basic knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills</p></li><li><p>Demonstrate some ability to influence within study team</p></li><li><p>Independently resolves most issues and complex matters, requiring advanced analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven track record in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related area. Additionally, ≥ 6 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in one or more of the following therapeutic areas is preferred – cardiovascular, renal, metabolic disease. Basic knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><p>(2 of 2)</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Accountant, Collaboration Accounting]]></title>
    <date><![CDATA[Sun, 22 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44571]]></requisitionid>
    <referencenumber><![CDATA[R44571]]></referencenumber>
    <apijobid><![CDATA[r44571]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44571/senior-accountant-collaboration-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>We seek a <strong>Senior Accountant</strong> within Collaboration Accounting, individual will be an active member of the monthly and quarterly close processes, with a high focus on accounting for our revenue generating agreements. The individual will also be responsible for preparing and analyzing various expense and balance sheet account analyses and will work closely with our Industrial Operation and Supply Chain team for all inventory related transactions that result in revenue generation. You will interact and partner with Accounting & Finance teams, senior leadership, and other business personnel to prepare schedules, present results, and accurately account for transactions. This position will provide exposure to a variety of unique and high-volume transactions, and will give you the opportunity to be a key contributor in interpreting and accurately accounting for the financial transactions resulting from Regeneron’s various Collaboration agreements. Individual will also be responsible for ensuring compliance with our SOX controls and Accounting policies and procedures. With the ongoing global expansion of Regeneron, you will be a key contributor in a growing and dynamic environment.</p><h3>A Typical Day in the Role Might Look Like:</h3><ul><li>Understand complex collaboration agreements, including, but not limited to, expense reimbursement, including the review of the related accounts receivable</li><li>Responsible for preparation and review of various expense schedules</li><li>Works directly with Finance to ensure completeness and accuracy of accruals and reclasses</li><li>Responsible for preparation and review of journal entries, supporting schedules, account analyses</li><li>Responsible for interaction with the Industrial Operation and Supply Chain Accounting team to ensure accurate reporting on the various Collaboration Inventory related transactions, along with the calculation of the related revenue and reimbursement</li><li>Responsible for preparation of P&L and Balance Sheet flux explanations for Management</li><li>Responsible for quarterly reconciliation of accounts receivable with Finance</li><li>Responsible for ensuring compliance with documented Accounting Policies and Sarbanes-Oxley controls</li><li>Participate in monthly and quarterly meetings with internal and external parties</li><li>Demonstrate knowledge of technical accounting standards under US GAAP, and its application to tasks at hand</li><li>Facilitate process improvement initiatives</li></ul><h3>This Role Might Be For You If You:</h3><ul><li>Have strong organizational abilities, attention to detail, and accuracy</li><li>Demonstrate excellent verbal and written communication skills, including, effective presentation skills</li><li>Are highly proficient with Microsoft applications is required</li></ul><p>This role requires a BS degree in Accounting, with CPA/CPA track preferred, with 3-5 year of relevant accounting experience. Experience with financial applications is preferred.</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>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Flow Cytometry]]></title>
    <date><![CDATA[Thu, 26 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45522]]></requisitionid>
    <referencenumber><![CDATA[R45522]]></referencenumber>
    <apijobid><![CDATA[r45522]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45522/associate-scientist-flow-cytometry/]]></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 highly motivated<strong> Associate</strong> Scientist – Flow Cytometry to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as data analysis using various flow cytometric software programs.</p><p><strong>As a Associate Scientist – Flow Cytometry, A Typical Day Might Include:</strong></p><ul><li><p>Ensuring proper maintenance, alignment, and calibration of cell sorting equipment</p></li><li><p>Analyzing flow cytometric data</p></li><li><p>Maintaining and organizing schedules for cell sorting equipment</p></li><li><p>Maintaining adequate inventory of flow cytometry supplies and reagents</p></li><li><p>Supporting maintenance of flow cytometry equipment, such as LSRFortessa X-20, FACSymphony A3/A5, FACSDiscovery A8, Aurora, CytoFLEX (LX), IntelliCyt iOue, and Amnis ImageStreamX MkII cytometers</p></li><li><p>Operating a Sony MA900, FACSFusion, FACSymphony S6, and FACSDiscovery S8 high-speed cell sorters</p></li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li><p>You are able to critically analyze and troubleshoot scientific problems</p></li><li><p>You have a customer-centric viewpoint</p></li><li><p>You have good scientific initiative and ability to multi-task, prioritize work and balance multiple projects</p></li><li><p>You can work independently but also within a collaborative team environment and have flexibility to work on changing priorities</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS in a scientific field and 1-3 years of relevant experience using cytometric instrumentation. Experimental laboratory work and cytometry sorting is strongly preferred. Must be flexible and willing to perform flow cytometric duties that expedite and support scientific staff's flow cytometric goals and objectives. Experiences with cell sorting, tissue culture, cytometry staining, assay development, and data analysis is advantageous. Additionally, we need someone with analytical problem-solving experience. </p><p><strong>#regncyto</strong></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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Feb 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, MASH]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45729]]></requisitionid>
    <referencenumber><![CDATA[R45729]]></referencenumber>
    <apijobid><![CDATA[r45729]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45729/senior-medical-director-medical-affairs-mash/]]></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><div>The Senior Medical Director, Medical Affairs – MASH, will play a pivotal and highly visible strategic leadership role within the organization, reporting directly to the VP, Medical Affairs, General Medicine. This role is responsible for driving the medical strategy and execution for MASH assets, with a strong focus on strategic planning, cross-functional leadership, and external engagement. The Senior Medical Director will ensure all medical affairs activities are delivered with scientific excellence, integrity, and patient-centricity.</div></div><div><div><div><div><p><strong>A typical day in this role might look like: </strong></p><ul><li>Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives. Champions the integration of scientific communications, publications, annual medical planning, and field communication strategies in partnership with key internal and external stakeholders.</li><li>Apply deep therapeutic area expertise and strategic business acumen to proactively identify and address evolving medical needs in clinical practice. Ensures the medically appropriate use of investigational medicines and anticipates future trends impacting patient care, policy, and access.</li><li>Directs and oversees the generation, management, and dissemination of robust clinical and non-clinical data. Drives high-impact publication strategies and ensures scientific content supports both the medical strategy and external stakeholder needs, maintaining the highest standards of accuracy and scientific rigor.</li><li>Leads cross-functional and cross-alliance teams with a focus on strategic alignment, collaboration, and excellence in execution. Fosters a culture of innovation and accountability, ensuring seamless coordination across medical, commercial, regulatory, and alliance partners.</li><li>Serves as a key strategic advisor and leader on global and US cross-functional teams, providing authoritative scientific and medical perspectives that inform and shape organizational strategy and decision-making.</li><li>Oversee the design, conduct, and reporting of Medical Affairs studies, ensuring scientific integrity, regulatory compliance, and alignment with strategic priorities. Provides mentorship and guidance to teams executing these initiatives.</li><li>Cultivates and expands long-term, strategic partnerships with clinical experts, societies, collaborative groups, advocacy organizations, payers, policy makers, and other external stakeholders. Acts as the primary ambassador for Regeneron, building trust and advancing shared goals in the MASH therapeutic area.</li><li>Leads prioritization and support for investigator-initiated studies, serving as a key decision-maker and member of internal Scientific Review Committees. Ensuring alignment with overall medical strategy and organizational objectives.</li><li>Overseas and ensures the scientific accuracy and compliance of all medical materials, including promotional and non-promotional content. Provides final approval and guidance to uphold the highest standards of scientific and ethical integrity.<br> </li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Must have an MD or MD equivalent with a preference for specialized fellowship training in Gastroenterology or Hepatology</li><li>5 years of related industry experience in global or US medical affairs</li><li>Solid background and experience in drug development and life-cycle management</li><li>Experience with working in an alliance setting strongly preferred</li><li>Ability to lead technical and business discussions internally and externally and explain scientific/medical concepts to all levels</li><li>Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields</li><li>Ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through on requests from key opinion leaders</li><li>Strong leadership and management skills</li><li>Attention to detail in analyses, deliverables, and communications</li><li>Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management</li><li>A proactive self-starter who can lead work and manage others independently, with the ability to see the next step and take actions without prompting</li><li>Ability to juggle multiple projects</li><li>Thorough understanding of the healthcare environment including all external stakeholders</li></ul><p>#MDJOBSMA, #MDJOBS, #GDMAJobs</p></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>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 16:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Lab Integration Developer]]></title>
    <date><![CDATA[Sat, 14 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45571]]></requisitionid>
    <referencenumber><![CDATA[R45571]]></referencenumber>
    <apijobid><![CDATA[r45571]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45571/principal-it-lab-integration-developer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal IT Lab Integration Developer is responsible for designing, developing, validating, and supporting integrations between laboratory systems, analytical instruments, enterprise platforms (LIMS), and data platforms within a regulated pharmaceutical environment. This role combines application development, system integration, data management, and regulatory compliance within a GMP-regulated laboratory environment.</p><p>As a Principal IT Lab Integration Developer, a typical day might include the following:</p><ul><li>Support the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Design and develop integrations between instruments and the Orchestration Layer.</li><li>Build and support API-based, file-based, and message-based integrations (REST, SOAP, SFTP, JSON, XML).</li><li>Provide level 2/3 support for QC Lab Systems.</li><li>Partner with QC Analysts, QA, IT infrastructure and external vendors.</li><li>Develop instrument data capture and automation workflows.</li><li>Configure and support middleware and integration platforms.</li><li>Ensure all integrations comply with GxP, 21 CFR Part 11, and data integrity (ALCOA+) requirements.</li><li>Participate in Computer System Validation (CSV/CSA) activities (IQ/OQ/PQ documentation).</li><li>Perform impact assessments and change control documentation.</li><li>Monitor and troubleshoot integration issues in production environments.</li><li>Collaborate with QC, R&D, Manufacturing, and QA teams.</li><li>Support audits and regulatory inspections.</li></ul><p>This role may be for you if you have:</p><ul><li>Skill in connecting various lab instruments (e.g., liquid handlers, analyzers) to central platforms like LIMS or ELNs to automate data capture and reduce manual transcription.</li><li>Knowledge of RESTful APIs, web services, and middleware tools used to bridge communication between the orchestration engine and disparate lab hardware.</li><li>Proficiency in languages such as Python or VBA for customizing automated workflows and data parsing.</li><li>Ability to understand data formats across different systems, ensure consistent values/naming conventions, and providing the correct data to the authorized locations </li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology, Math or related field and </p><ul><li>Senior: 5 years of relevant experience or equivalent combination of education and experience.</li><li>Principal: 8 years of relevant experience or equivalent combination of education and experience.</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 15 Mar 2026 09:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - Midlands]]></title>
    <date><![CDATA[Mon, 02 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44889]]></requisitionid>
    <referencenumber><![CDATA[R44889]]></referencenumber>
    <apijobid><![CDATA[r44889]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44889/sales-specialist-midlands/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>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.</div><div><div><div><div><p>This role is focused on the maintenance and growth of key accounts within the Midlands 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 dermatology 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></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Mar 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Omnichannel Customer Experience, Consumer Marketing (Ophthalmology)]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46178]]></requisitionid>
    <referencenumber><![CDATA[R46178]]></referencenumber>
    <apijobid><![CDATA[r46178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46178/associate-director-omnichannel-customer-experience-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[<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><p><strong>A Typical Day Might Look Like This:</strong></p><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><p><strong>If This Looks Like You:</strong></p><ul><li><p>Demonstrated competency in managing consumer/patient marketing programs</p></li><li><p>Demonstrated digital and social marketing experience</p></li><li><p>Demonstrated ability to work effectively, efficiently, and collaboratively with team members and across departments to develop and execute programs and materials</p></li><li><p>Demonstrated competency in agency management and budget management</p></li><li><p>Proven ability to work within regulatory, legal, and compliance guidelines</p></li><li><p>Demonstrated project management skills</p></li></ul><p>To be considered you have a Bachelor's Degree, MBA a plus. Demonstrated experience in marketing of biologics preferred. You have 10+ years of progressive marketing experience including at least 5 years in the Consumer space in pharmaceutical marketing. Demonstrated omnichannel digital marketing experience. Demonstrated Consumer marketing competencies in the pharmaceutical/biotech areas. Prior U.S. launch experience a plus. Strong interpersonal & presentation skills. Ability to communicate with all levels of the organization. Must be willing to travel ~10% (including weekend travel as needed). This is an office-based role, and the expectation will be to work in the office 4-days a week.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Program Operations Leader, Internal Medicines]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44524]]></requisitionid>
    <referencenumber><![CDATA[R44524]]></referencenumber>
    <apijobid><![CDATA[r44524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44524/director-program-operations-leader-internal-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director Program Operations Leader</strong> (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><strong>Director Program Operations Leader - Specialty Medicine, Rare Disease</strong></p><p><em>(For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days from home. A fully remote role is NOT possible for this position.)</em></p><p><strong>In a typical day, you will:</strong></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><strong>To be considered, you must possess</strong> 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><em>For US Locations, this position is on-site 4 days per week and 1 day from home. </em></p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 04:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46370]]></requisitionid>
    <referencenumber><![CDATA[R46370]]></referencenumber>
    <apijobid><![CDATA[r46370]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46370/drug-production-associate-manufacturing-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 Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment. Please continue to review the job duties if you are interested in working 3rd shift (10pm-8:30am) with the potential for weekends.</p><p>A typical day for a Drug Production, Associate Manufacturing Specialist might include:</p><ul><li><p>Performing all aspects of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operating automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Supporting equipment start-up, troubleshooting, and validation</p></li><li><p>Partnering with R&D teams to implement new drug manufacturing processes and technologies</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Enjoy working 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>Are highly organized, detail oriented and perform work accurately the first time</p></li><li><p>Value trust and transparency in everyday work</p></li><li><p>Work well in both small and large teams to accomplish tasks adhering to a schedule</p></li><li><p>Can 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>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Are a good communicator and can give and receive feedback constructively</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>Gowning and Environment</p><ul><li><p>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>Shift & Physical Requirements</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.</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>To be considered for this role you must meet the below minimum education and experience requirements:</p><p>Drug Production, Associate Manufacturing Specialist:</p><ul><li><p>HS diploma + 4 years of relevant work experience <strong>or</strong></p></li><li><p>AS, BS or BA in Life Sciences or related field</p></li><li><p>Able to work 3rd shift (10pm-8:30am) with the potential for weekends</p></li></ul><p>Regeneron offers an exciting and competitive benefits package! For details check out: <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a></p><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 (hourly)</strong></strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Biostatistics - Thrombosis]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46415]]></requisitionid>
    <referencenumber><![CDATA[R46415]]></referencenumber>
    <apijobid><![CDATA[r46415]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46415/associate-director-biostatistics-thrombosis/]]></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>This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development. </p></div><div><div><div><div><div><div><div><div><div><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></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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Marketing (Hematology)]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43748]]></requisitionid>
    <referencenumber><![CDATA[R43748]]></referencenumber>
    <apijobid><![CDATA[r43748]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43748/associate-director-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we are dedicated to transforming lives through science and innovation. We are seeking a dynamic and entrepreneurial Associate Director Marketing Hematology to join our team in the UK & Ireland.</p><p>This hybrid role blends sales and marketing expertise, offering you the opportunity to build the commercial success of our Haematology portfolio while adapting global strategies to meet local market needs. If you’re passionate about driving impactful results and thrive in a collaborative environment, this role is for you.</p><p>In this position, you’ll play a pivotal role in adapting and implementing global brand plans, ensuring flawless cooperation across cross-functional teams, and championing Regeneron’s values in everything you do. This position offers growth opportunities as the portfolio expands, making it an exciting time to join Regeneron.</p><h3><strong>A Typical Day:</strong></h3><ul><li>Develop and implement brand plans for the Haematology portfolio, aligning efforts and budgets with growth objectives and global strategy.</li><li>Adapt and gain approval for UK-specific materials derived from global resources, ensuring minimal changes while maintaining compliance.</li><li>Own the development of launch strategies, account planning, and commercial advisory boards to optimize market understanding and opportunities.</li><li>Build and implement National, Regional, and Local account plans with clear prioritisation and trade-offs to achieve commercial success.</li><li>Expand Regeneron’s reputation and relationships with key healthcare professionals across therapy areas.</li><li>Collaborate with cross-functional colleagues to analyse market dynamics and trends, supporting brand and collaboration objectives.</li><li>Maintain the highest ethical and compliance standards while encouraging positive relationships with internal and external stakeholders.</li></ul><h3><strong>This Role May Be For You If:</strong></h3><ul><li>Are a self-starter with an ambitious mindset, capable of blending local strategy with global objectives while keeping things simple and actionable.</li><li>Thrive in a hybrid role that demands adaptability, prioritisation, and a hands-on approach to ensure commercial success.</li><li>Excel at building relationships and credibility with KOLs partners.</li><li>Possess excellent planning, communication, and presentation skills, and are comfortable navigating CRM systems and sales data.</li><li>Are willing to travel 30–40% of the time, including occasional weekends for conferences and meetings.</li><li>Have a passion for maintaining ethical standards and aligning with our values.</li></ul><h3><strong>To Be Considered:</strong></h3><p>The ideal candidate will hold a BS/BA degree (Master’s degree or advanced certifications preferred) and have over 10 years of biopharma experience, including proven success as a sales manager and marketer. Strong leadership and communication skills are crucial, along with proficiency in English (a second European language is advantageous). Experience in immunology or biologics and established relationships with oncology KOLs are highly desirable.</p><p>Join us in making a meaningful impact in Haematology while advancing your career in a role that blends strategy, execution, and collaboration.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Integration Engineer]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44508]]></requisitionid>
    <referencenumber><![CDATA[R44508]]></referencenumber>
    <apijobid><![CDATA[r44508]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44508/senior-automation-integration-engineer/]]></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[<div><div><p>We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems. </p></div><div><p>As a Senior Automation Systems Integration Engineer<strong>,</strong> a typical day might include the following: </p></div><div><ul><li><p>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures. </p></li></ul></div><div><ul><li><p>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems. </p></li></ul></div><div><ul><li><p>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines. </p></li></ul></div><div><ul><li><p>Supporting small manufacturing, engineering, and validation projects. </p></li></ul></div><div><ul><li><p>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action. </p></li></ul></div><div><ul><li><p>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols. </p></li></ul></div><div><ul><li><p>Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure </p></li></ul></div><div><ul><li><p>Creation, modification, and maintenance of automation system documentation </p></li></ul></div><div><p>This role might be for you if you: </p></div><div><ul><li><p>Have experience with OT applications, including SCADAs, HMIs, Historians, etc. </p></li></ul></div><div><ul><li><p>Are familiar with standing up large systems at the enterprise level </p></li></ul></div><div><ul><li><p>Have core knowledge related to ISE S95 and S88 principles and IT/Automation integration </p></li></ul></div><div><ul><li><p>Have familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure </p></li></ul></div><div><ul><li><p>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better </p></li></ul></div><div><ul><li><p>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly </p></li></ul></div><div><ul><li><p>Can balance changing priorities with increasing workload by making/communicating timely decisions </p></li></ul></div><div><p>To be considered for the Senior Automation Systems Integration Engineer position you ideally should have a bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level: </p></div><div><ul><li><p>Senior Engineer: 5+ years </p></li></ul></div></div><div><div><ul><li><p>Principal Engineer: 8+ years</p></li></ul></div><div><p>Level will be determined based on qualifications relevant to the role</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 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>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Scientific Communications ( Oncology)]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46060]]></requisitionid>
    <referencenumber><![CDATA[R46060]]></referencenumber>
    <apijobid><![CDATA[r46060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46060/associate-director-scientific-communications-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>We are seeking an Associate Director, Scientific Communications, to join our dynamic Global Medical Affairs team supporting out Oncology portfolio. In this pivotal role, you will shape and implement comprehensive scientific communication strategies for oncology, ensuring alignment with therapeutic goals and delivering impactful educational materials. This position offers the opportunity to collaborate within a matrix organization, influence medical communications globally, and contribute meaningfully to advancing patient care. </p><p>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits.</p><p><strong>A typical day may include the following: </strong><br>• Developing and maintaining scientific communication platforms, lexicons, and disease-state education materials.<br>• Collaborating with Medical Affairs Franchise Directors aligning on congress deliverables and educational content.<br>• Driving quality control and endorsement of scientific assets like program slides and publication updates.<br>• Leading projects through medical review committees to ensure compliance and scientific accuracy.<br>• Managing vendor interactions to ensure timely delivery of high-quality materials.<br>• Creating innovative digital scientific assets for diverse medical channels, including portals and social media.<br>• Assessing internal and external medical education needs to develop impactful educational activities.<br>• Supervising budget allocations and ensuring systematic tracking of expenditures.<br>• Maintaining centralized, searchable resource repositories to support internal teams.</p><p><strong>This may be for you if you:</strong> <br>• Are highly self-motivated with a hands-on execution mentality and a “can-do” spirit. <br>• Excel in a fast-paced, constantly evolving organization and value adaptability. <br>• Are passionate about ensuring scientific integrity and accuracy in all medical and scientific assets. <br>• Enjoy collaborating across multifunctional teams and driving innovative approaches to medical education. <br>• Are committed to ethical standards and prioritize patient-first values in your work. <br>• Are adept at using digital channels to enhance the reach and impact of scientific communications. </p><p>To qualify for this position, you must hold a PhD, MD, or PharmD and have a minimum of 6 years of experience in the pharmaceutical industry, including at least 4 years in Scientific Communications or Medical Affairs. A strong background in oncology and general medicines is essential. Preferred qualifications include proficiency in managing vendor relationships, developing innovative digital assets, and navigating medical review processes. <br> </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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Scientific Communications- General Medicine]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46059]]></requisitionid>
    <referencenumber><![CDATA[R46059]]></referencenumber>
    <apijobid><![CDATA[r46059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46059/director-scientific-communications-general-medicine/]]></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 our passionate team as the Director of Scientific Communications for General Medicine. In this pivotal role, you will lead the creation and alignment of our integrated medical communication strategies to advance medical knowledge and improve clinical care for patients. Collaborating with cross-functional teams, we develop evidence-based scientific communication platforms, ensuring content accuracy, accessibility, and impact. With a focus on innovation and collaboration, this role offers the opportunity to make meaningful contributions to partner engagement and patient outcomes.<br>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Lead the development and execution of comprehensive Integrated Medical Communication Plans. <br>• Establish and communicate clear scientific communication of our objectives and tactical plans<br>• Partner with medical directors and key collaborators to devise congress strategies and oversee deliverables. <br>• Drive the creation of scientific and digital communication materials, including scientific communication platforms, lexicons, narratives, and disease-state education.<br>• Collaborate with the Congress Strategy and Planning team to ensure impactful booth designs and materials.<br>• Assess medical education gaps and find opportunities to create tailored, targeted, and timely content for diverse platforms and regions.<br>• Oversee the medical review process to ensure scientific accuracy, compliance, and ethical integrity of all materials.<br>• Manage project budgets and timelines in collaboration with the project manager.</p><p>T<strong>his may be for you if you: </strong><br>• Thrive in a collaborative, cross-functional environment. <br>• Can manage multiple projects, vendors, and priorities in a fast-paced environment. <br>• Are committed to ethical and compliance standards and have a “patient-first” value framework. <br>• Bring critical thinking and analytical skills to assess data and inform strategic decision-making. </p><p>To be considered it is required to have a PhD, MD, or PharmD with at least 8 years of relevant medical communication experience. Demonstrated expertise in medical communication strategies, congress planning, scientific content development, and medical education is required. Strong project management skills, ethical integrity, and the ability to work in a matrix organization are essential. <br> </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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 14:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Flow Cytometry]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45896]]></requisitionid>
    <referencenumber><![CDATA[R45896]]></referencenumber>
    <apijobid><![CDATA[r45896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45896/associate-scientist-flow-cytometry/]]></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 highly motivated<strong> Associate Scientist – Flow Cytometry</strong> to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as perform data analysis using various flow cytometric software programs.</p><p><strong>As an Associate Scientist – Flow Cytometry, a typical day might include:</strong></p><ul><li><p>Ensuring proper maintenance, alignment, and calibration of cell sorting equipment</p></li><li><p>Analyzing flow cytometric data</p></li><li><p>Maintaining and organizing schedules for cell sorting equipment</p></li><li><p>Maintaining adequate inventory of flow cytometry supplies and reagents</p></li><li><p>Supporting maintenance of flow cytometry equipment, such as LSRFortessa X-20, FACSymphony A3/A5, FACSDiscover A8, Aurora, CytoFLEX (LX), IntelliCyt iQue, and Amnis ImageStreamX MkII cytometers</p></li><li><p>Operating a Sony MA900, FACSAria Fusion, FACSymphony S6, and FACSDiscover S8 high-speed cell sorters</p></li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li><p>You are able to critically analyze and troubleshoot scientific problems</p></li><li><p>You have a customer-centric viewpoint</p></li><li><p>You have good scientific initiative and ability to multi-task, prioritize work, and balance multiple projects</p></li><li><p>You can work independently but also within a collaborative team environment and have flexibility to work on changing priorities</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS in a scientific field and 1-3 years of relevant experience using cytometric instrumentation. Experimental laboratory work and cell sorting is strongly preferred. Must be flexible and willing to perform flow cytometric duties that expedite and support scientific staff's flow cytometric goals and objectives. Experience with cell sorting, tissue culture, cytometry staining, assay development, and data analysis is advantageous. Additionally, we need someone with analytical problem-solving experience. </p><p><strong>#regncyto</strong></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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Research (Neuroscience)]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42013]]></requisitionid>
    <referencenumber><![CDATA[R42013]]></referencenumber>
    <apijobid><![CDATA[r42013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42013/vice-president-research-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>Seeking experienced, rigorous, and innovative leader to direct Regeneron’s Neuroscience research team, consisting of approximately 50 dynamic researchers currently focusing on development of therapeutics against neurodegenerative diseases, motor neuron disease, chronic pain, and neuropsychiatric disorders, utilizing biologics and genetic medicines. Successful candidate would direct and inspire Neuroscience’s preclinical team by using their deep and broad expertise to set strategic vision, suggest novel technological approaches, and critically evaluate data and projects. Candidate would be expected to participate in translational activities, progressing drug targets along the pipeline from early research through clinical development. Candidate would also participate in Regeneron’s broader scientific community, participating actively in cross-functional meetings and representing Regeneron’s Neuroscience vision to Senior Leadership and external collaborators. </p><p><strong>As a Vice President of Neuroscience Research a typical day might look like: </strong></p><ul><li>Directly supervise Regeneron’s senior Neuroscience leadership team and manage the broader group, providing vision, inspiration, and both short-term and long-term goals. Communicate priorities, policies, and goals of Regeneron Senior Leadership to the broader Neuroscience group.</li><li>Identify new strategies or technologies, including genetic medicines, for pursuing novel targets and approaches.</li><li>Set priorities and ensure progression of, or go/no-go decisions for, targets and projects. Be familiar with processes and procedures for moving targets from preclinical research through the development pipeline.</li><li>Actively participate in departmental, cross-functional, senior leadership, and external meetings to contribute neuroscience expertise and to represent the goals and vision of the Neuroscience group.</li><li>Interact broadly and collaboratively with other therapeutic focus areas and technology groups within the company, forging relationships and active collaborations, as well as leveraging technologies to advance neuroscience research as a systems-level endeavor.</li><li>Identify and mentor the Neuroscience group, providing opportunities, visibility, and challenge in order to develop all group members to their maximum scientific and professional potential.</li><li>Conduct or oversee review of neuroscience-related documents, including regulatory submissions, manuscripts, contracts, etc. </li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Both deep and broad expertise in the field of Neuroscience essential.</li><li>Familiarity with cutting edge technology, including genetics medicines, and proven experience applying technology to neuroscience-related questions essential.</li><li>Strong written and oral communication skills with the ability to communicate both science and vision essential.</li><li>Strong leadership skills with managerial and mentorship experience and excellence essential.</li><li>Experience with administratively directing a group (managing budget and organization, etc.) essential.</li><li>Exposure to drug development or similar regulated activities highly desirable.</li><li>Broad network of colleagues and collaborators, strong publication record, and national/international reputation desirable.</li><li>At least 10 years experience after PhD; 20+ years desirable; a minimum of 5 years in an industry or translational setting.</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 and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</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>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development  AI Engineer]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43611]]></requisitionid>
    <referencenumber><![CDATA[R43611]]></referencenumber>
    <apijobid><![CDATA[r43611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43611/senior-manager-global-development-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>Global Development (GD) is embarking on a digital transformation project that will incorporate AI, machine learning, and automation into our processes to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. This position will play a key role in developing the platforms, processes and technologies that will incorporate AI effectively across GD. The AI engineer will work with a team of engineers and scientists to help bring transformative change to GD. The role will encompass a wide range of AI/ML-related activities, from data engineering and technical development to optimizing vendor systems for use at Regeneron to mentoring colleagues in best practices for adopting and AI in their everyday workflows. Development will not necessarily be limited to the use of generative AI, but may also include technical implementation of machine learning models, natural language processing, and other approaches. The engineer will work with stakeholders across GD and Regeneron (e.g. enterprise IT, commercial, research, etc.) to develop solutions and architectures that not only address GD’s needs but also integrate into the overall corporate strategy.</p><div><div><div><div><p><strong>As a Senior Manager, a typical day may include: </strong></p><ul><li><p>Implement, and refine novel algorithms and scalable AI /ML solutions tailored to GD applications such as clinical trial design, regulatory intelligence, patient identification and stratification, etc. Deploy these solutions to production environments as appropriate Implementation includes hands-on development and coding.</p></li><li><p>Develop, implement, and improve data architecture and engineering approaches for diverse data sources across GD</p></li><li><p>Contribute to initiatives with GDIT and enterprise IT to build the necessary infrastructure (software and hardware) to support advanced analytics</p></li><li><p>Collaborate with GD colleagues to help them approach AI/ML more effectively</p></li><li><p>Establish rigorous validation frameworks for AI models and monitor existing models for accuracy and efficiency</p></li><li><p>Stay up to date with the latest advances in the field and, as appropriate, evaluate them for adoption at Regeneron</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Deep understanding of generative AI, machine learning, natural language processing, and statistical modeling</p></li><li><p>Deep expertise in programming (Python, R, etc.), with a focus on applying advanced technical skills to data analysis, pipeline creation, automation, and software development</p></li><li><p>Expertise in database platforms and cloud computing infrastructure</p></li><li><p>Track record of model development, implementation to scale, maintenance, and evaluation in a healthcare of life sciences setting</p></li><li><p>Experience managing and analyzing large-scale clinical datasets</p></li><li><p>Excellent communication skills, both technical and non-technical</p></li><li><p>Experience managing multiple projects</p></li><li><p>Experience working in cross-functional teams</p></li><li><p>May require travel up to 20%</p></li></ul></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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation System Administrator]]></title>
    <date><![CDATA[Sun, 21 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43991]]></requisitionid>
    <referencenumber><![CDATA[R43991]]></referencenumber>
    <apijobid><![CDATA[r43991]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43991/senior-automation-system-administrator/]]></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>As a Senior Automation System Administrator, you will be embedded in a tight-knit team responsible for administration of automated/computerized system software and firmware to meet cGMP and policy requirements. In this critical role our team specifies and maintains software configuration for biopharmaceutical process, monitoring, and testing systems. This involves evaluation of new software for functional equivalence, validation activities to demonstrate suitability of software/process and maintaining the qualified state of systems throughout their lifecycle through change control.</p><p>In this role, a typical day might include:</p><ul><li>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</li><li>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</li><li>Utilizing configuration management and recipe/method management.</li><li>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</li><li>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</li><li>Conducting system integration with existing systems (e.g. LIMS, Historian).</li><li>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and/or design specifications, test plans, technical evaluation, and quality risk assessments.</li><li>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</li><li>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</li><li>Leading aspects of the work for contractors and providing guidance as applicable.</li></ul><p>This role might be for you if you:</p><ul><li>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</li><li>Have interest in manufacturing process within a regulated technical environment.</li><li>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</li><li>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</li><li>Understand process control systems and product release testing systems.</li><li>Are familiar with regulatory and quality policies, procedures, documentation methods.</li><li>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</li><li>Enjoy project management and have strong organizational skills.</li><li>Are motivated to participate in continuous process improvement.</li></ul><p>Applicants ideally should have a BS/BA in Science, Engineering or related field and the following minimum relevant experience for each level:</p><ul><li>Senior Automation System Administrator: 5+ years</li><li>Principal Automation System Administrator: 8+ years</li></ul><p>Equivalent combination of education and experience may be considered. Level will be determined based on qualifications relevant to the role.</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>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Associate Scientist- Neuroscience]]></title>
    <date><![CDATA[Wed, 21 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44714]]></requisitionid>
    <referencenumber><![CDATA[R44714]]></referencenumber>
    <apijobid><![CDATA[r44714]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44714/temp-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>This Associate Scientist position will support preclinical research in the Neurotherapeutics area, with focus on Parkinson’s disease. The selected individual will support the design and execution of experiments to understand the mechanisms of neurodegenerative diseases, discover new therapeutic targets and validate novel therapeutic strategies. Primary duties include in vitro and in vivo studies that involve handling live rodents for tasks such as behavioral testing, injections, surgeries and sample collection and processing. Additionally, the successful candidate will have the opportunity to characterize collected samples using biochemical, molecular, and immune-based assays at the bench as well as develop in vitro assays. Candidates with passion for scientific discovery and dedicated to high quality research are strongly encouraged to apply. </p><p><strong>As an Associate Scientist, a typical day might include:</strong></p><ul><li><p>Planning, initiating, and completing the following types of in vivo assays: cell line maintenance, in vitro experiments, standardized behavioral tests, injections, rodent surgeries, sample collections.</p></li><li><p>Planning, initiating, and completing the following types of biochemical, molecular, and immune-based assays: ELISAs, western blotting, immunofluorescence, immunohistochemistry and RT-qPCR.</p></li><li><p>Learning new methods and/or technologies relevant to various projects including, but not limited to, stereotactic delivery of drugs, flow cytometry and others.</p></li><li><p>Accurately documenting findings and lab records in an electronic laboratory notebook</p></li><li><p>Presenting data in formal and informal meetings.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have strong organizational and time-management.</p></li><li><p>You can work effectively as part of a team as well as independently.</p></li><li><p>You have the ability to work on multiple projects and prioritize as needed.</p></li></ul><p><strong>To be considered for this role, </strong>you must possess a bachelor's or master's degree in a related field along with a minimum of two years of experience in biology, molecular biology, neuroscience, or a related biological science. Experience with in vitro and animal models of brain disorders, histology, tissue preparation, is strongly preferred. Some understanding of neurodegenerative disorders is preferable.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 22 Jan 2026 15:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Medicine, Clinical Scientist (Ophthalmology)]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44659]]></requisitionid>
    <referencenumber><![CDATA[R44659]]></referencenumber>
    <apijobid><![CDATA[r44659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44659/senior-manager-internal-medicine-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[<p>The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3>As a Senior Manager in Clinical Sciences, a typical day may include the following:</h3><ul><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Develops/maintains 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>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Collaborates with internal functions and external vendors to promote clinical study integrity</p></li><li><p>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Demonstrated ability to influence within team and may influence cross functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements.</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally.</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in Ophthalmology clinical trials.</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Allergy & Immunology]]></title>
    <date><![CDATA[Tue, 03 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44729]]></requisitionid>
    <referencenumber><![CDATA[R44729]]></referencenumber>
    <apijobid><![CDATA[r44729]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44729/medical-director-clinical-development-allergy-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[<div>The Medical Director, Clinical Sciences is responsible for facilitating assigned studies, providing investigator support of Regeneron driven studies, and may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into the Clinical Program Lead, Clinical Sciences and is expected to have proficient knowledge of the drug development process, good clinical practice, study design and research methodology as well as understand Regulatory and compliance landscape in the pharmaceutical industry. This role utilizes scientific and clinical expertise to initiate, propose, design and execute research and development programs for early and/or late stage assets. This role may be suitable for an Allergist, Immunologist, Pulmonologist, or Dermatologist. Some industry experience preferred.</div><div><div><div><div><p>A typical day in the life may include the following responsibilities:</p><ul><li>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program. Clinical deliverables may include individual protocols; clinical components of regulatory documents/registration dossier and brand related medical information, clinical communication and publications</li><li>Demonstrated ability to influence team and may influence across function</li><li>Ability to lead activities within a matrix environment</li><li>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally</li><li>Advanced analytical and influencing skills</li><li>Ability to communicate concise and clear messages</li><li>Seeks to understand different perspectives and cultures and values differing points of view</li><li>Can identify critical risks and mitigation</li><li>Proficient medical writing skills and advanced presentation skills</li></ul><p>This role may be for you if:</p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p>In order to be considered for this role, a M.D. degree or equivalent is required. Specialized clinical fellowship training in Allergy, Immunology, Pulmonology, or Dermatology is strongly preferred. 0-4 years of clinical development experience in industry is preferred, but academic research experience will be considered.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p></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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Feb 2026 12:26:28 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Boundary Systems Lead (Oracle Fusion)]]></title>
    <date><![CDATA[Wed, 04 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44207]]></requisitionid>
    <referencenumber><![CDATA[R44207]]></referencenumber>
    <apijobid><![CDATA[r44207]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44207/director-erp-boundary-systems-lead-oracle-fusion/]]></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 Oracle Fusion ERP Boundary Systems Lead provides functional and technical oversight for key boundary applications supporting the Oracle Fusion Cloud modernization program—including but not limited to Icertis (Contract Lifecycle Management), Reval (Treasury), Zycus (iSource), Concur (Travel & Expenses), Serengeti, Pas-X MES, Kinaxis-APS, Veeva Vault, LIMS, Tracelink, Orchestrate, BlueMountain, Tririga, and Nemo (Contractor Management). The role ensures these systems align with future-state Oracle Cloud processes, support phased transitions from Oracle EBS, and effectively enable Procurement, Finance, and Supply Chain operations. The individual partners with GPOs, Product Leads, SMEs, SI partners, and Oracle Support to review designs, resolve system gaps, oversee integration impacts, pursue enhancements, and ensure boundary applications remain stable, compliant, and fully integrated into the ERP landscape.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Serve as the primary SME for the boundary systems listed above throughout the ERP modernization program.</p></li><li><p>Manage Statements of Work (SOWs) for boundary systems, including coordination with vendors and internal teams for effort estimation, resource planning, and tracking deliverables.</p></li><li><p>Manage and work in a “3 in a box” model, collaborating closely with Business stakeholders and System Integrators to ensure alignment, effective communication, and successful delivery across all boundary-system initiatives.</p></li><li><p>Oversee and manage resources associated with boundary systems, ensuring effective resource utilization and engagement.</p></li><li><p>Review and validate SI partner functional and technical designs impacting boundary systems; challenge and refine solutions to ensure optimal alignment with business needs and Oracle Cloud standards.</p></li><li><p>Ensure boundary-system functionality, configurations, workflows, and data structures support end-to-end processes across P2P, R2R, O2C, Plan to Make, PLM/PDH, WMS, OTM/GTM, and EPM Cloud.</p></li><li><p>Assess and resolve functional and technical gaps related to boundary systems; coordinate with Oracle Support and Oracle Development on SRs, enhancement requests, and roadmap clarifications.</p></li><li><p>Support phased ERP deployment—including coexistence with Oracle EBS and transition to Oracle Cloud—and ensure boundary systems adapt to evolving processes and designs.</p></li><li><p>Collaborate with the Integration Lead to understand cross-system dependencies, including OIC middleware flows, REST/SOAP web services, outbound/inbound integrations, BIP/FBDI interfaces, and file-based patterns (without owning the integration build).</p></li><li><p>Lead and oversee reconciliation efforts to ensure data accuracy, completeness, and consistency between Oracle Fusion Cloud and boundary applications.</p></li><li><p>Coordinate with SI partners on integration requirements, error-handling expectations, and sequencing of boundary-system interactions with Oracle Cloud.</p></li><li><p>Identify compliant, practical workarounds to avoid implementation blockers while long-term solutions or Oracle enhancements are pursued.</p></li></ul><h3><strong>This Job Might Be For You If You Have:</strong></h3><br><ul><li><p>Understanding of business processes and Oracle Fusion Cloud modules across Source-Procure to Pay, Record to Report, Supplier Management, Supply Chain, Plan to Make, PLM, Order to Cash related domains.</p></li><li><p>Expertise with Oracle Fusion Cloud and key boundary systems related to domains listed above.</p></li><li><p>Proficiency in managing SOWs, effort estimation, and resource utilization</p></li><li><p>Solid understanding of integration technologies (OIC, APIs, file-based interfaces)</p></li><li><p>Experience with data reconciliation and compliance requirements (SOX, GxP, 21 CFR Part 11)</p></li><li><p>Strong documentation, analytical, and cross-functional collaboration skills</p></li><li><p>Exposure to working with 3PLs, CMOs and other enterprise boundary systems</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><br><ul><li><p>Bachelor’s degree in Computer Science, Information Systems, Engineering, or a related field</p></li><li><p>15+ years of experience with enterprise ERP applications</p></li><li><p>10+ years working on with key boundary systems (e.g., Icertis, Reval, Zycus (iSource), Concur, Serengeti, Pas-X MES, Kinaxis-APS, Veeva Vault, LIMS, Tracelink, Orchestrate, BlueMountain, Tririga and Nemo)</p></li><li><p>Proven track record in large-scale ERP transformation programs (Oracle Fusion Cloud preferred)</p></li></ul><br><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[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Feb 2026 09:56:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Las Vegas]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45033]]></requisitionid>
    <referencenumber><![CDATA[R45033]]></referencenumber>
    <apijobid><![CDATA[r45033]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45033/medical-specialist-i-dermatology-las-vegas/]]></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[<p><strong>Geography: Las Vegas, Nevada</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><ul></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><p>To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44611]]></requisitionid>
    <referencenumber><![CDATA[R44611]]></referencenumber>
    <apijobid><![CDATA[r44611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44611/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>A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies.</p><p><strong>In this role, a typical day might include:</strong> ​</p><p>As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in 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. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.</p><p><strong>This role might be for you if can:</strong> ​</p><ul><li>Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. </li><li>Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. </li><li>Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).</li><li>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. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.</li><li>Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</li><li>Participate in department working groups; provide input in development of tools and improvement of processes.</li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>Masters Degree</li><li>SAS, (Base, Stat, Macro, graph). </li><li>3 + Years experience</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead (Genetics Medicine, Hepatology)]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45358]]></requisitionid>
    <referencenumber><![CDATA[R45358]]></referencenumber>
    <apijobid><![CDATA[r45358]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45358/senior-manager-clinical-study-lead-genetics-medicine-hepatology/]]></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 <strong>Senior Clinical Study Lead</strong> (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is 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 out-sourced 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>This role is not eligible fully remote. This role is required to be onsite in one of our locations.</p><h3><strong>A typical day in this role looks like: </strong></h3><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Provides operational input into protocol development</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Ensures compliance with the clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors</p></li><li><p>Provides input into baseline budget development and management</p></li><li><p>Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level</p></li><li><p>Leads the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Oversees/conducts site evaluation and selection</p></li><li><p>Leads investigator meeting preparation and execution</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</p></li><li><p>Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Ensures accurate budget management and scope changes for internal and external studies</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Oversees the execution of the clinical study against planned timelines, deliverables and budget</p></li><li><p>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</p></li><li><p>Ensure clinical project audit and inspection readiness through the study lifecycle</p></li><li><p>Supports internal audit and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>Contributes to clinical study report writing and review</p></li><li><p>Facilitates and contributes to study level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables</p></li><li><p>Recommends and participates in cross-functional and departmental process improvement initiatives</p></li><li><p>Responsible for identification of innovative approaches to clinical study execution including global considerations 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><li><p>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require 25% travel</p></li></ul><h3><strong>This role may be for you if you have:</strong></h3><ul><li><p>Exceptional interpersonal & leadership skills</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Advanced communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Strong budget management experience</p></li><li><p>An awareness of relevant industry trends</p></li><li><p>Ability to build, lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Advanced project management skills, cross-functional team leadership and organizational skills</p></li><li><p>Line management experience</p></li></ul><p><strong>In order to be considered qualified, </strong>a minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience.</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Deployment & Incentives]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45419]]></requisitionid>
    <referencenumber><![CDATA[R45419]]></referencenumber>
    <apijobid><![CDATA[r45419]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45419/associate-director-field-deployment-incentives/]]></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 seeking an Associate Director of Field Deployment and Incentives to join our organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Associate Director of Field Deployment and Incentives serves as a strategic leader, responsible for enhancing field engagement and performance by designing and implementing IC plans, contests, and awards, and optimizing field force structure and territory alignments to achieve organizational objectives.</p><p>As a key member of the field enablement team, you will be the primary point of contact for your designated therapeutic areas, serving as a trusted strategic partner to field leadership and internal stakeholders. You will proactively provide essential insights and develop strategies for IC, contests, awards, and field force alignments by transforming complex data into clear, actionable recommendations that facilitate data-driven decision-making. Your expertise in project and vendor management will ensure that all deliverables meet the highest standards of quality and timeliness.</p><p>This role presents a unique opportunity to directly impact field performance and corporate outcomes, fostering professional growth and expanding skill sets within a dynamic team environment.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Lead end‑to‑end IC design (plans, contests, awards) aligned to brand and corporate objectives, ensuring solutions are motivational, equitable, compliant, and fiscally responsible.</p></li><li><p>Engage with field force structure and sizing projects, leading expansions, re-structures, and quarterly alignments changes to optimize field deployment and minimize field disruption.</p></li><li><p>Develop and execute robust models and simulations to assess incentives, contests, awards, and field structure design options and their trade-offs, effectively communicating implications and recommendations to facilitate real-time, data-driven decision-making for field leaders and senior stakeholders.</p></li><li><p>Partner with Insights/Marketing/Advanced Analytics to inform IC and award strategy, contest design and objectives, territory coverage and workload, aligning on methodologies and assumptions across teams.</p></li><li><p>Develop communication/training materials to ensure a high level of field understanding of their IC plans, contests, awards, and territory/geography design.</p></li><li><p>Liaise with external vendors and internal partners to ensure the design and delivery of high-quality, fit-for-purpose, actionable tools and reports.</p></li><li><p>Establish and maintain IC governance (policies, business rules, SOPs), partner across Legal/Compliance/Finance/HR/Marketing/Data-Management teams, and drive quality, accuracy, and timeliness in all deliverables.</p></li><li><p>Ensure a unified metric framework and consistent definitions across IC, contests, and performance reporting measures.</p></li><li><p>Address data discrepancies and collaborate with Commercial Data Management to uphold high data integrity. Prioritize, triage, and resolve issues swiftly and clearly, maintaining field trust in our processes and deliverables.</p></li><li><p>Own operations calendar and cross-functional operating rhythm, covering everything from territory design to performance tracking and payouts. Ensure that key timelines are consistently communicated to both field personnel and internal stakeholders and leaders.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong> </p><ul><li><p>Minimum BA/BS with 10+ years (or MBA/MS with 7+ years) of progressive experience in the pharmaceutical industry, focusing on IC, field force size, structure, and alignments, field analytics, targeting, or call planning, with 6+ years directly related to IC and field force structure and alignments.</p></li><li><p>Bachelor’s degree in a quantitative field, business, or related discipline; an advanced degree is preferred. </p></li><li><p>Subject-matter expertise in pharmaceutical incentive compensation and field deployment best practices.</p></li><li><p>Hands-on experience in analytics and modeling using large, complex datasets to solve intricate business challenges.</p></li><li><p>Proven ability to distill complex analyses into clear and actionable recommendations.</p></li><li><p>Strong QC/validation rigor.</p></li><li><p>Exceptional communication and interpersonal skills, with a demonstrated ability to influence without authority and collaborate effectively with diverse teams.</p></li><li><p>Excellent project management and prioritization skills to effectively balance multiple projects and priorities.</p></li><li><p>Able to thrive in fast-paced and ambiguous environments while consistently delivering exceptional results.</p></li><li><p>Solid understanding of open/closed pharma distribution models.</p></li><li><p>Proficient in Excel and PowerPoint for executive‑ready deliverables.</p></li><li><p>Expertise with key pharmaceutical data sources, including Xponent, DDD, 867, specialty pharmacy, patient-level, Hub, among others.</p></li><li><p>Knowledge of programming languages such as SQL, R, and Python.</p></li></ul><p><em>Preferred Qualifications include:</em></p><ul><li><p>Experience in sub-national performance analytics, including territory/region KPIs, execution diagnostics, and pull-through measurement.</p></li><li><p>Familiarity with data management and analytics platforms like Databricks or Snowflake, as well as business intelligence and visualization tools such as Power BI or Tableau.</p></li><li><p>Experience applying AI / Machine Learning to field deployment tools and design.</p></li><li><p>Knowledge of CRM Systems such as Veeva and Salesforce.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Clinical Experimental Sciences)]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44465]]></requisitionid>
    <referencenumber><![CDATA[R44465]]></referencenumber>
    <apijobid><![CDATA[r44465]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44465/senior-manager-clinical-study-lead-clinical-experimental-sciences/]]></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><em>This role is not eligible remote, and must be onsite in one of our US office locations.</em></p><p>The <strong>Senior Clinical Study Lead (CSL) – Clinical Experimental Sciences Operations (CES Ops)</strong> is accountable for the execution of assigned clinical studies/research collaborations from study design, through execution, to study close out. Additionally, there are responsibilities for initiation, oversight and completion of CES Ops continuous improvement and Strategic Imperatives workstreams. The Sr. CSL is accountable for oversight of the contract and budget execution, study timelines, study budget management, and ensuring study conduct is in accordance with, Regeneron Standard Operating Procedures (SOPs), CES Ops Business Practice Tool processes and ICH/GCP, as applicable. The CES Ops portfolio is dynamic in nature; study types include, but are not limited to, less complex data transfer agreements, retrospective sample/data acquisition studies to more complex prospective studies including sample/data acquisition, biomarker/technology/method validation, genotypic/phenotypic call back studies, and challenge/screening studies. This role will interface heavily with Basic Research/Discovery as well as with clinical site staff, predominately at academic institutions. In rare instances the more complex studies may require out-sourcing to Clinical Research Organizations (CROs); the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives. This role may be responsible for direct line management.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Leads the cross-functional study team responsible for clinical study/research collaboration delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</li><li>Provides operational input into research plan and/or study protocol development</li><li>Ensures development of study specific documentation such as samples management plans and data management plans are completed on time and in accordance with the study protocol.</li><li>Oversees set-up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc.</li><li>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors, if appropriate</li><li>Provides input into baseline timeline development and management</li><li>Provides input into baseline budget development and management, facilitates internal review of the study budget for assessment of Fair Market Value</li><li>Ensures accurate budget management and scope changes for internal and external studies</li><li>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</li><li>Oversees the execution of the clinical study against planned timelines, deliverables and budget</li><li>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the</li><li>scope of work</li><li>Manages and oversees study close-out activities</li><li>Ensures End of Study Summary is delivered and properly archived</li><li>Facilitates and contributes to study level lessons learned</li><li>Assigns tasks to Clinical Study Management staff and supports their deliverables</li><li>Recommends and participates in cross-functional and departmental process improvement initiatives</li><li>Responsible for identification of innovative approaches to clinical study execution including global considerations and continuous improvement departmental processes and procedures</li><li>Works with Therapeutic Focus Area groups within Basic Research/Discovery</li><li>Works closely with clinical site staff, predominantly at academic institutions</li><li>Expected to maintain higher volume and/or greater complexity studies</li><li>Expected to communicate learnings, best practices and relevant information to other study leads at all levels, ensures consistency and internal alignment across staff</li><li>May be responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree and8+ years of relevant clinical experience is required.</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 18:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Manager Supplier Quality and Compliance]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44089]]></requisitionid>
    <referencenumber><![CDATA[R44089]]></referencenumber>
    <apijobid><![CDATA[r44089]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44089/sr-manager-supplier-quality-and-compliance/]]></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>We are currently looking to fill a Sr Manager Supplier Quality and Compliance. In this role you will be responsible for overseeing a team that supports and maintains all cGMP compliance aspects of procurement operations. Some of the major activities include but are not limited to the following: management and facilitation of the Approved Supplier List (ASL), deviation investigations, CAPAs, supplier audit closures and evidence follow up, support of regulatory inspections, SOP writing and revision, change controls, and the management of the development of a Supplier Corrective Action Report (SCAR) management process via the compliance function. Additional responsibilities include other compliance tasks and functions as assigned.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Ensures that the team operates as a global cohesive unit taking advantage of the efficiencies and ensuring compliance for all IOPS sites.</p></li><li><p>Tracks progress on all Strategic Sourcing & Procurement quality system deliverables, including deviation investigations, CAPAs and change controls, ensuring quality and accuracy of documentation as well as adherence to established due dates.</p></li><li><p>Interfaces regularly with Quality Assurance and other functional areas to remove obstacles, resolve conflicts, and to help facilitate critical decisions pertaining to quality system deliverables.</p></li><li><p>Monitors, reports, and responds to Key Performance Indicators (KPIs) for the compliance functions, e.g. right-first-time (RFT) for deviation investigations.</p></li><li><p>Performs deviation investigations and coordinates CAPA implementation as needed for high risk events.</p></li><li><p>Proactively manages and maintains all Procurement cGMP procedures, documentation and training related to SOPs and Work Instructions.</p></li><li><p>Continually reassess’ Strategic Sourcing & Procurement systems and processes for adherence to cGMPs and industry best practices and implements changes/improvements as needed. </p></li><li><p>Represents the Strategic Sourcing & Procurement department on various topics during regulatory inspections, and coordinates responses to inspection observations as applicable.</p></li><li><p>Supports the start-up/integration of Strategic Sourcing & Procurement compliance functions at other IOPS sites, including travel as needed.</p></li></ul><p>This role may be a fit for you if you:</p><ul><li><p>Can oversee and direct the maintenance of the Approved Supplier List (ASL) and associated Periodic Review of suppliers.</p></li><li><p>Drive successful audit closures by focusing on proactive issue resolutions and communication with suppliers to effect acceptable audit closures and gathering of evidence of closure for raw material and component suppliers.</p></li><li><p>Can lead the coordination with Cross Functional Compliance resources to support procurement and Quality Auditing needs for acceptable closure of Internal Regeneron and Supplier audit findings and to secure evidence that substantiates commitments. Tracks and reports CAPA in support of audit closure.</p></li><li><p>Have the ability to work closely with Legal, QA and suppliers to help facilitate the execution and management of Master Services Agreements, Quality Agreements, etc. as required.</p></li><li><p>Can action on the procurement responses to compliance related requests for data from Regulatory, Quality Assurance, Audit staff and other stakeholders.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and the following amount of relevant experience:</p><ul><li><p>Sr Manager level: 8+ years of relevant experience, with at least 5 years of relevant experience in a cGMP environment or equivalent combination of education and experience.</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>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Sr Manager, Commercial Operations]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44875]]></requisitionid>
    <referencenumber><![CDATA[R44875]]></referencenumber>
    <apijobid><![CDATA[r44875]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44875/temp-sr-manager-commercial-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager Commercial Operations (Contractor) drives data‑led decision‑making across Commercial Operations by developing and delivering business intelligence strategies, leading analytics projects, and translating sophisticated data into actionable insights.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Lead the build and execution of strategies in partnership with Commercial Operations, Sales, Marketing, and external partners.</p></li><li><p>Scope and handle analytics projects that extract, integrate, and analyze customer and market data from multiple sources to answer strategic and tactical business questions.</p></li><li><p>Own and improve critical commercial tools and platforms, ensuring high data quality, reliability, and usability.</p></li><li><p>Conduct sophisticated analyses to identify performance trends, generate insights, and advise resource allocation, channel mix, and sales force efficiency.</p></li><li><p>Define, track, and communicate critical metrics and leading indicators across teams; maintain dashboards and reporting cadences for collaborators and senior leadership.</p></li><li><p>Deliver clear, compelling presentations and insight narratives that influence decision‑making and drive action.</p></li><li><p>Ensure compliance with corporate policies, privacy, and data governance standards; implement controls and documentation for reproducibility and audit readiness.</p></li><li><p>Collaborate with IT and global analytics teams to build scalable data solutions, automate data pipelines, and modernize analytics products.</p></li><li><p>Support forecasting, segmentation, and targeting initiatives using sophisticated modeling and experimentation techniques.</p></li><li><p>Partner with alliance and above‑market teams to harmonize definitions, share standard processes, and enable consistent measurement across regions.</p></li><li><p>Establish analytics SOPs, playbooks, and reviewer guides; standardize code, QA processes, and release management for dashboards and models.</p></li><li><p>Proactively identify issues, risks, and data gaps; recommend pragmatic solutions and secure alignment across cross‑functional collaborators.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Experience leading commercial analytics and business intelligence initiatives from concept through deployment and adoption.</p></li><li><p>Hands‑on expertise with CRM and marketing platforms (e.g., Veeva CRM, PromoMats) and modern BI tools (e.g., Power BI, Tableau, Qlik) to build and scale dashboards.</p></li><li><p>Strong proficiency in data wrangling and analysis (e.g., SQL and one or more of Python or R), and familiarity with data modeling and automation practices.</p></li><li><p>methodologies to support sales and marketing planning.</p></li><li><p>Deep understanding of data governance, privacy, and compliance principles; comfortable working with cross‑functional IT, Data, and Compliance partners.</p></li><li><p>Excellent storytelling, presentation, and collaborator leadership skills; ability to translate analytics into clear business recommendations.</p></li><li><p>A track record of building collaboration across matrixed teams and influencing without direct authority.</p></li><li><p>This role is a 12 month contract.</p></li></ul><p><strong>To Be Considered:</strong><br>You bring a bachelor’s degree in a quantitative or relevant field with 8+ years of relevant experience, with at least 5+ in pharmaceutical or life‑science.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Operations Specialist (IT Business Process Automation)]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44091]]></requisitionid>
    <referencenumber><![CDATA[R44091]]></referencenumber>
    <apijobid><![CDATA[r44091]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44091/principal-operations-specialist-it-business-process-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Principal Operations Specialist (IT Business Process Automation) to lead ServiceNow and ProcessX automation for IAM and QAR in a GxP environment. Own workflow design, platform optimization, incident response, and audit readiness.</p><p>As a Principal Operations Specialist , a typical day might include the following:</p><ul><li>Design, build, and maintain automated workflows in ServiceNow and ProcessX to improve operational efficiency and service delivery.</li><li>Identify, scope, and prioritize automation opportunities across IAM and QAR, aligned to business goals and regulatory standards.</li><li>Optimize platform configurations and integrations for performance, scalability, and compliance—following ITIL and GxP best practices.</li><li>Monitor and continuously improve service availability, reliability, and throughput against defined SLAs/OLAs.</li><li>Define and enforce operational guardrails, SOPs, and validation artifacts to ensure GxP, security, and audit readiness.</li><li>Lead major incident response for automation-driven services; coordinate resolution, communicate with stakeholders, and conduct post-incident reviews.</li><li>Create and execute Service Improvement Plans; use data and analytics to measure impact and recommend enhancements.</li><li>Act as a trusted advisor to stakeholders—translate requirements into practical automation solutions and clear roadmaps.</li></ul><p>This role may be for you if you have:</p><ul><li>Deep hands-on experience with ServiceNow workflow configuration, custom development, and integrations.</li><li>Proven success implementing automation that improves efficiency and compliance in GxP contexts.</li><li>Strong familiarity with IAM and QAR processes in regulated environments.</li><li>Expertise with ITIL disciplines (Incident, Problem, Change, Reporting, Monitoring).</li><li>Experience operating in validated systems with GAMP 5 concepts and data integrity controls.</li><li>Process and workflow orchestration.</li><li>Familiarity with audit frameworks and documentation for validation packages.</li><li>ServiceNow certifications (e.g., CSA, CAD, CIS in relevant modules).</li><li>Technologies: ServiceNow platform, Flow Designer, IntegrationHub, CMDB, ProcessX (or equivalent GxP workflow platform).</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and</p><ul><li>Senior: 5 years of experience delivering IT/OT services to business or consumers</li><li>Principal: 8 years of experience delivering IT/OT services to business or consumers</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Strong GxP experience and proven experience in highly regulated environments required</li><li>Service Management or support in a large-scale and diverse environment of incident management, escalation procedures and related disciplines</li><li>Experience with delivering projects and initiatives in the IT or OT space.</li><li>Deep experience with ITIL disciplines</li><li>Experience with operating systems (Microsoft Windows & Linux), VMware.</li><li>Experience with monitoring and security tools such as Splunk, Claroty and next Gen OT tools.</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director PPM Data Stewardship Lead]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45539]]></requisitionid>
    <referencenumber><![CDATA[R45539]]></referencenumber>
    <apijobid><![CDATA[r45539]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45539/director-ppm-data-stewardship-lead/]]></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>Director Data Stewardship Lead</strong> (Director Level) is a strategic enterprise role responsible for establishing and leading the data stewardship function at the portfolio level. This individual will define the vision, strategy, and operating model for stewardship, ensuring data integrity, accessibility, and consistency to enable enterprise planning, portfolio insights, and informed decision-making. They will work closely with Data Governance, the key system Business Process Owner (e.g. Planisware, Planview), Portfolio Management, Program and Project Planning, DADS (Data Analytics & Data Science), and domain data owners to operationalize stewardship practices and embed robust data standards, quality frameworks, and analytical capabilities into the organization’s core operations. This role carries responsibility to build out and lead a team over time, enabling the maturation and scaling of the stewardship function.</p><p><em>***NOTE: This role must be onsite 4-days per week in either our Tarrytown, NY or Warren, NJ office and is NOT eligible remote.</em></p><p><strong>A typical day in this role: </strong> </p><ul><li>Establish and lead the data stewardship function, including defining the strategic vision, operating model, and foundational processes, with a roadmap to build and lead a dedicated team over time.</li><li>Partner with Data Governance to build upon and implement enterprise-wide data policies, standards, and SOPs that support regulatory compliance and business objectives.</li><li>Collaborate with system Business Process Owners and Program, Portfolio Management and Project Planning Lead to align stewardship practices with enterprise planning systems and processes.</li><li>Work closely with DADS (Data Analytics & Data Science) to ensure stewardship activities support enterprise analytics, data products, and AI/ML initiatives.</li><li>Curate and maintain business metadata (definitions, glossary terms, business rules) to promote consistent data understanding and usage across functional domains.</li><li>Ensure the quality, integrity, and completeness of portfolio-level data (study/program timelines, resource, financial, and operational metadata), including definition of data quality metrics and remediation plans.</li><li>Design and oversee development of dashboards and reports to monitor stewardship performance, operational data quality, and portfolio trends, enabling data-driven decision making.</li><li>Lead data integration and migration initiatives, ensuring seamless alignment between legacy systems and enterprise data platforms.</li><li>Champion a data-driven culture by developing training, guidance, and communication strategies that empower business users to adopt governed data practices.</li><li>Continuously assess and integrate emerging technologies (e.g., AI/GenAI) to enhance metadata management, anomaly detection, and stewardship efficiency.</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Extensive knowledge of drug development, project planning, and data management, with expertise in implementing data governance policies and upholding data quality standards.</li><li>Proficient in project planning and analytics software such as Planisware, Microsoft Project, OnePager, and Microsoft Office (Word, Excel, PowerPoint), including dashboard and report creation.</li><li>Strong analytical, communication, and collaboration skills, with the ability to identify, report, and escalate risks, and convey complex data insights to diverse stakeholders.</li><li>Experienced in managing and monitoring data quality processes, including validation, reconciliation, and continuous improvement across study, program, resource, and financial data.</li><li>Skilled in designing and maintaining metrics, dashboards, and reports to track operational performance, resource utilization, and financial outcomes.</li><li>Proven ability to provide training and guidance on data stewardship best practices, facilitate alignment on data standards, and support adoption of new data environments and tools.</li><li>Committed to staying current with industry trends, regulatory requirements, and emerging technologies to enhance data stewardship and analytics capabilities.</li></ul><p><strong>In order to be considered qualified for this role, </strong>a minimum of a Bachelors Degree and 12+ years in data management, analytics, resource management, or related roles, with at least 5 years in a leadership or strategic capacity</p><ul><li>Data management or governance certifications (e.g., CDMP) and/or PMI Project Management Professional (PMP) is 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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, HR Business Partner]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43727]]></requisitionid>
    <referencenumber><![CDATA[R43727]]></referencenumber>
    <apijobid><![CDATA[r43727]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43727/manager-hr-business-partner/]]></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>Regeneron is seeking a Manager, HR Business Partner (HRBP) to support Regeneron’s R&pD (Research and Preclinical Development). This role will report into the Director, HR Business Partner.</p><p><strong><em>This role is based at our Global HQ in Tarrytown, NY with a minimum of 4 days onsite required - this is not open to fully remote / hybrid work.</em></strong></p><p>At Regeneron, an HRBP develops solutions to solve business challenges in order to increase their ability to deliver on our mission - utilizing science to bring new medicines to patients. You will be partnering with other HRBP’s, COE functions within HR, and other key stakeholders to provide support and counsel to the business managers / employees on organizational and people related issues. This will include talent acquisition & planning, onboarding and development, employee engagement, culture, performance management, and change management to promote and maintain REGN’s high-performance culture, the Regeneron Way.</p><p>Key to this will also be your ability to quickly develop trusted relationships with people at all levels within R&pD as well as a strong partnership with your Sr. HRBP’s and COE partners. You have to be comfortable with challenging the status quo, influencing scientifically trained leaders and delivering key HRBP support in a fast-paced culture. Being able to pivot is key. This role acts as a champion and a coach for our expanding business.</p><p><br><strong>As a Manager, HRBP a typical day may include:</strong></p><ul><li>Partners with the HRBP Leadership to identify and plan key HR work for the business functions. This role works across all client groups. </li><li>Working with managers and employees to help solve any employee relations, people related challenges, keeping in mind precedence and business needs including partnering with internal HR specialists </li><li>Handling conflicts, investigations, and employee grievances.</li><li>Providing coaching to managers and employees with an emphasis on helping the person understand what their options are for each situation and how to demonstrate the Regeneron Way</li><li>Participating in interviews for key positions, as well as candidate debriefs to help drive the best hiring decisions in a rapidly expanding organization </li><li>Onboarding new managers by partnering with hiring managers to facilitate and support a successful onboarding experience </li><li>Identifying needs (individual and team) within client areas and partner with the OD Consulting team to craft solutions that will address business needs (e.g., team building)</li><li>Partnering with Total Rewards to define new roles, identify external comparable/market value of positions and other reward/recognition programs </li><li>Partnering with managers to support year-end performance calibrations as well as year-end compensation in Workday</li><li>Ad hoc project support (e.g., career ladders, re-organization projects)</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You are able to quickly develop trusted relationships with peers and employees at all levels.</li><li>You are comfortable with challenging the status quo in a growing team and influencing scientific and technical leaders.</li><li>You are learning agile and comfortable with a high level of ambiguity</li><li>You have strong analytical skills and you use data to identify problems and deliver solutions that will benefit employees</li><li>You have exceptional employee relations skills and experience</li></ul><p><strong>To be considered for this role you must possess a Bachelor’s degree in a scientific or HR related discipline; advanced degrees such as MBA, or Master’s in OD / IO or Human Resources is preferred. Minimum of 7-9years’ HR experience, with experience working within the pharma/biopharma/biotech or Manufacturing industry highly preferred.</strong></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>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations (GMP IT/OT)]]></title>
    <date><![CDATA[Tue, 24 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43879]]></requisitionid>
    <referencenumber><![CDATA[R43879]]></referencenumber>
    <apijobid><![CDATA[r43879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>The Associate Director of IT Operations (GMP IT/OT) ensures the reliable operation, delivery, and management of IT/Operational Technology (IT/OT) infrastructure and services, with a focus on supporting a highly regulated GxP environment. This role provides strategic direction, operational management, and administrative oversight for the daily IT operational activities, including hardware, communications & WiFi infrastructure, and service delivery. The position also ensures integration and alignment with corporate IT systems and infrastructure while maintaining robust compliance, security, and service standards.</p><div><div><div><div><p>As an Associate Director of IT Operations (IT/OT), a typical day might include the following:</p><ul><li>Ensure the reliable operation of IT/OT infrastructure, including but not limited to servers, hardware, communications and desktop support, plus oversight of daily operational activities.</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.</li><li>Build scalable and secure wireless networks to support industrial and enterprise needs. </li><li>Provide operational management for data centre operations, network services, telecom, asset management, and security plus ensure systems and procedures are in place for effective monitoring and reporting. </li><li>Maintain compliance with industry standards, including experience with automation systems such as DeltaV/Emerson and Rockwell/Allen-Bradley.</li><li>Manage service providers to ensure high-quality service delivery and alignment to service level agreements (SLAs) and act as the escalation point for major incidents.</li><li>Ensure compliance with relevant regulations and standards, including GxP, FDA and other global regulatory requirements. </li><li>Maintain robust security measures to protect IT/OT infrastructure, including data integrity and disaster recovery planning. </li><li> Lead and mentor a diverse technical team and run recruitment, training, performance evaluations, and target setting for the IT Operations team. </li><li>Collaborate with partners to ensure seamless integration between IT and OT systems. </li><li>Provide regular management reporting on service performance and IT operations. </li></ul><p>This role may be for you if you:</p><ul><li>Management and delivery experience required including management of a diverse technical team, including Helpdesk, Desktop, Server and Network staff. Experiencing managing vendors and managed services.</li><li>Experience in developing and deploying SLA's, Metrics and other best practices as well as having successfully implemented ITIL practices into an organization.</li><li>Experience with Business Continuity and Disaster Recovery planning.</li><li>Strong background in Microsoft OS in particular Server and GPO elements.</li><li>Strong understanding of Data Integrity and associated tools.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with</p><ul><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><li>Preferred knowledge of understanding of IT compliance guidelines, including PICS, CFR21 Part 11, Annex 11, and GAMP.</li></ul></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>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Feb 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr EDC Development]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45329]]></requisitionid>
    <referencenumber><![CDATA[R45329]]></referencenumber>
    <apijobid><![CDATA[r45329]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45329/sr-mgr-edc-development/]]></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>We’re growing our Clinical Database Development team, and we’re looking for a thoughtful leader to help us deliver reliable, inspection‑ready EDC solutions that support our key development programs. We provide clear direction, consistent processes across studies, and caring mentorship so our developers and CRO partners can do their best work. We champion quality standards and regulatory requirements, and we celebrate practical, elegant builds in Medidata Rave. We’ll support you as you guide strategy, develop talent, and shape the standards that move our portfolio forward!</p><p><strong>A Typical Day:</strong></p><ul><li>Oversee CRO EDC database builds and ensure process compliance.</li><li>Build and configure Rave studies using our Global Library.</li><li>Program edit checks, dynamics, derivations, and custom functions.</li><li>Lead UAT setup in Cloud Administration and drive resolution to go‑live.</li><li>Configure Coder, TSDV, and Clinical Views as protocols require.</li><li>Manage amendments, migrations, and quick publishes with Rave tools.</li></ul><p><strong>This Role May Be For You if you:</strong></p><ul><li>Balance standards with protocol nuances to craft dependable Rave builds.</li><li>Guide CRO partners with clarity while maintaining consistent practices.</li><li>Value compliance—21 CFR Part 11, ICH‑GCP, and CDISC are second nature.</li><li>Move comfortably between strategy, oversight, and hands‑on configuration.</li><li>Enjoy coaching developers and contributing to a high‑quality global library.</li></ul><p><strong>To Be Considered</strong><br>A bachelor’s degree in mathematics, science, or a related field is required, along with <strong>8+ years of EDC development</strong> experience in biotechnology, pharmaceutical, or health‑related industries and <strong>3+ years of people‑management</strong> experience. <strong>Medidata Rave</strong> experience is required, and you bring thorough knowledge of Data Management and Clinical Database Development processes and of applicable regulations (<strong>21 CFR Part 11, ICH‑GCP, CDISC</strong> standards for data collection). Preferred qualifications include <strong>Medidata Builder Certification</strong>, <strong>C#</strong> programming knowledge, and <strong>TrialGrid</strong> familiarity, plus experience with Rave Amendment Manager and Medidata Cloud Administration.</p></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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Quality Technical Operations]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45585]]></requisitionid>
    <referencenumber><![CDATA[R45585]]></referencenumber>
    <apijobid><![CDATA[r45585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45585/director-quality-technical-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>Regeneron is hiring! As the Director of Quality Technical Operations you will lead a high-impact Quality function spanning QA MES, QA Validation Oversight, and QA Tech Transfer. You’ll define and implement cGMP best practices, set quality standards and metrics, and ensure clinical and commercial manufacturing operations meet and exceed regulatory compliance requirements.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Define and implement quality standards, systems, and metrics across clinical and commercial manufacturing operations.</p></li><li><p>Provide quality oversight to activities related to validation and ensure that they are effectively administered and comply with regulatory requirements.</p></li><li><p>Oversee QA tasks related to electronic manufacturing record management and tech transfer.</p></li><li><p>Compile, organize, and present quality metrics and trends to senior leadership.</p></li><li><p>Plan and allocate QA resources to meet program goals, timelines, and priorities.</p></li><li><p>Coordinate prioritization of activities with area management to optimize execution.</p></li><li><p>Prepare for regulatory and customer audits; ensure observations are addressed effectively and on schedule.</p></li><li><p>Maintain safety and operational standards and approve documents related to QA functions.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven leadership in cGMP environments with hands-on experience in QA systems and metrics.</p></li><li><p>A track record of successful audit readiness, execution, and response management.</p></li><li><p>Strong collaboration, communication, and stakeholder engagement skills.</p></li><li><p>An understanding of bulk API biologics manufacturing operations.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Life Sciences or related field and the following amount of relevant pharmaceutical manufacturing experience for each level:</p><ul><li><p>Director – 12+ years</p></li><li><p>Sr Director – 15+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role. May substitute proven experience for education requirement.</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>$172,200.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 17:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vet Technician]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45471]]></requisitionid>
    <referencenumber><![CDATA[R45471]]></referencenumber>
    <apijobid><![CDATA[r45471]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45471/vet-technician/]]></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>Regeneron is seeking a highly motivated Vet Tech to assist our Veterinarians and Vivarium Management in administering a program of health and welfare to the rodent barrier and conventional colonies. </p></div><div><p><strong>A typical day as a Veterinary Technician might look like: </strong></p></div><div><ul><li><p>Provides clinical support for rodent health care including but not limited to sick checks, anesthesia, analgesia, euthanasia and surgery. </p></li></ul></div><div><ul><li><p>Coordinates/assists with transfers of rodents within and between facilities. </p></li></ul></div><div><ul><li><p>Performs health surveillance sampling. </p></li></ul></div><div><ul><li><p>Conducts Post Approval Monitoring of housing/procedure rooms. </p></li></ul></div><div><ul><li><p>Assists with training program for animal husbandry staff and research staff utilizing animals. </p></li></ul></div><div><ul><li><p>Pursues continuing education in lab animal medicine and managerial/leadership courses on TalentHub. </p></li></ul></div><div><ul><li><p>Prepares a presentation and presents at one monthly Veterinary Services seminar per year. </p></li><li><p>Rotating weekend on-call and on-site work over winter break is required.</p></li></ul></div><div><p><strong>This may be the role for you if: </strong></p></div><div><ul><li><p>You enjoy working within a team and can collaborate with colleagues. </p></li></ul></div><div><ul><li><p>You are willing to help to train and advise less experienced research staff. </p></li></ul></div><div><ul><li><p>You are meticulous and can produce work that typically does not need to be reviewed upon completion. </p></li></ul></div><div><p>You must have an Associates Degree in a relevant field and a minimum of 2 years of relevant technical experience with mice and rats in a laboratory setting. LVT and AALAS certification at the LAT level is desirable. Ideally you should have experience with anesthesia, analgesia and phlebotomy in rodents. We would also prefer a candidate with knowledge of applicable regulations regarding the accurate standards of animal care and use in a research environment. </p></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>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 12:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Scientist - Analytical and Biological Mass Spectrometry (ABMS)]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45875]]></requisitionid>
    <referencenumber><![CDATA[R45875]]></referencenumber>
    <apijobid><![CDATA[r45875]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45875/sr-scientist-analytical-and-biological-mass-spectrometry-abms/]]></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>Regeneron Pharmaceutical's Analytical and Biological Mass Spectrometry Group (ABMS), located in Tarrytown, NY is seeking a highly motivated Sr. Scientist. In this role, you will work in an innovative mass spectrometry lab and develop LC-MS methods for characterizing biotherapeutic products to support all stages of drug development, from early-stage candidate selections to late-stage regulatory submissions. You will conduct and develop innovative technologies to support a diverse Regeneron's R&D pipeline.</p><h3><strong>A Typical Day In This Role Looks Like:</strong></h3><ul><li>Lead and deliver on characterization activities to elucidate product quality attributes like post-translational modifications, sequence variants, charge variants, size variants, and host cell proteins.</li><li>Provide technical support for cross-functional teams, including formulation development, upstream and downstream process development, manufacturing and help to tackle real-time development challenges in process development and manufacturing for OOS/OOT investigations.</li><li>Proactively find opportunities to advance LC-MS analysis of biotherapeutics by developing technical innovations that will contribute to future developmental needs and/or efficiency gains.</li><li>Perform sample preparation and LC-MS-based experiments independently based on SOPs and document experiments, results and findings in electronic laboratory notebook (ELN).</li><li>Prepare and review regulatory submission documents like IND, comparability, and BLA reports, as well as manuscripts for publication in peer-reviewed journals.</li><li>Serve as the team representative, provide analytical expertise to cross-functional teams, and present findings at internal and external meetings.</li></ul><h3><strong>This Role May Be For You If:</strong></h3><ul><li>You thrive in a fast-paced, collaborative environment and consistently deliver results with efficiency and ownership.</li><li>You quickly learn new technologies, tackle complex problems, and have a passion for science.</li><li>You are self-motivated and proactive, prioritizing effectively, and driving work forward with minimal supervision.</li></ul><p>To be considered for this role, you must have a BS (10+ years), MS (7+ years) or PhD degree (0-3+ years) in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related field. Extensive experience with advanced mass spectrometers (Orbitrap, Q-TOF, Triple Quadrupole, etc.), liquid chromatography, and data processing software (Proteome Discoverer, Skyline, Protein Metrics, etc.) is desired. Knowledge and experience with extended characterization of monoclonal antibodies by mass spectrometry to support cell line and upstream/downstream development is a plus. Experience with automated liquid-handling systems (e.g., Bravo, KingFisher) and with experimental design and data analysis (e.g., design of experiments, molecular modeling, graphing, and statistical analysis software such as JMP) is a plus.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology-Des Moines, Iowa]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45725]]></requisitionid>
    <referencenumber><![CDATA[R45725]]></referencenumber>
    <apijobid><![CDATA[r45725]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45725/medical-specialist-i-dermatology-des-moines-iowa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Des Moines]]></city>
    <state><![CDATA[Iowa]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Specialist, Dermatology (MS) Des Moines/Iowa</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Principal Scientist - Clinical Imaging]]></title>
    <date><![CDATA[Mon, 02 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R38993]]></requisitionid>
    <referencenumber><![CDATA[R38993]]></referencenumber>
    <apijobid><![CDATA[r38993]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r38993/sr-principal-scientist-clinical-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>The Senior Principal Scientist is responsible for spearheading the imaging biomarker strategy and implementation across cardiovascular and metabolic indications in early- and late-phase clinical trials. This role involves collaboration with cross-functional study teams where you will lead the design of complex imaging approaches to test the efficacy and safety of Regeneron products. In this role, you will be responsible for developing and validating novel imaging-based biomarkers to address the needs of the Regeneron experimental therapies.</p><p>As a Senior Principal Scientist in Clinical Imaging you will:</p><ul><li>Collaborate closely with Research and Global Development colleagues to formulate appropriate imaging biomarker strategies to inform and advance the Regeneron clinical pipeline.</li><li>Provide leadership during the strategy phase of study design, guiding the team on all imaging aspects of the study, presenting the imaging components of the integrated biomarker strategy to senior management for endorsement, and authoring of key study documents.</li><li>Work closely with Clinical Imaging Operations and Clinical Trial Management to ensure the delivery of high-quality imaging data in clinical studies. This includes drafting imaging manuals and other documents for the trial, supporting the clinical team during the study start-up phase, and monitoring data integrity throughout the trial.</li><li>Supervise imaging Clinical Research Organizations (CROs) to ensure execution of imaging components in the trial, timely address any image quality issues, and ensure flawless delivery of key study imaging data and achievements</li><li>Identify gaps in imaging assessments for particular indications and propose novel biomarkers, and spearhead validation through collaboration with other functions within Regeneron or external institutions.</li><li>Support regulatory submission packages as the imaging subject matter expert</li></ul><p>This role requires that you:</p><ul><li>Work efficiently in a fast-paced, collaborative environment</li><li>Communicate extremely effectively across clinical teams and functions, and with senior management</li><li>Possess a broad knowledge of imaging and understand the challenges of image standardization across sites and countries</li><li>Have strong analytical and problem-solving skills</li><li>Thrive in addressing complex problems with innovative methods</li></ul><p>To be considered for this position, we expect you to have completed a PhD or MD/PhD program, with a minimum of 6 years of experience in clinical imaging, specifically within cardiovascular and/or metabolic domains. We believe you should have extensive expertise in the acquisition and analysis of various imaging modalities, including MRI, CT, ultrasound, and echocardiography. While experience in industry-sponsored clinical trials is preferred, it is not mandatory.</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>$148,300.00 - $241,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Mar 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Quality Compliance (Complaints)]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45407]]></requisitionid>
    <referencenumber><![CDATA[R45407]]></referencenumber>
    <apijobid><![CDATA[r45407]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45407/manager-quality-compliance-complaints/]]></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>Regeneron is currently looking for a Manager, Quality Compliance (Compliant Investigations).This role will lead a team providing QA oversight of site compliance, with a primary focus on product quality complaint and trend investigations for commercial and clinical products. This role reviews and approves documentation, evaluates evidence and records (internal and external), designs experiments to test hypotheses, and authors technical reports/protocols to support investigation conclusions. The manager partners cross-functionally with Manufacturing (internal/external), Quality Control, Quality Assurance, and Global Patient Safety to meet regulatory requirements and site standards, advising on compliance best practices and stepping in as needed to meet timelines and resolve issues.</p><p>As a Manager Quality Compliance, a typical day might include the following:</p><ul><li>Responsible for ensuring aspects of Quality Compliance for the Rensselaer site inclusive of manufacturing, quality control, validation, facilities, and materials management; this work may be done through direct reports.</li><li>Oversees investigations (product quality complaints and trending) related to dissatisfaction by end user related to commercial and clinical products.</li><li>Provides guidance on investigation plans related to complaints documentations, photographic evidence, return samples and is available support investigations.</li><li>Participates in regulatory and customer audits.</li><li>Identify gaps in systems and develop feasible plans for correction</li><li>Mentor direct reports and functional area counterparts in compliance requirements.</li><li>Facilitating continuous improvement initiatives specific to function.</li><li>Ensuring appropriate training programs are implemented for related to function.</li><li>Other related responsibilities as assigned.</li></ul><p>This role may be for you if you:</p><ul><li>Have previous quality experience in the pharmaceutical industry</li><li>You continuously seek to improve processes for improved performance</li><li>Enjoy leading a team of Quality minded professionals</li><li>Have knowledge/exposure to project management</li><li>Have proficiency in Microsoft Office Programs</li></ul><p>To be considered for the Manager Quality Compliance you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Life Sciences or related field. For various levels you must have the following:</p><ul><li>Assoc Manager, Quality Compliance: 6+ years</li><li>Manager, Quality Compliance: 7+ years</li><li>Sr. Manager, Quality Compliance: 8+ years</li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</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>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Délégué(e) Hospitalier(e) Oncologie - Bourgogne Franche-Comté]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45656]]></requisitionid>
    <referencenumber><![CDATA[R45656]]></referencenumber>
    <apijobid><![CDATA[r45656]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45656/delegue-e-hospitalier-e-oncologie-bourgogne-franche-comte/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>As an Oncology Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, while covering <strong>Bourgogne Franche-Comté</strong>. You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>Oncology Pharmaceutical Representative - Bourgogne Franche-Comté</strong></p><p><strong>As an Oncology Pharmaceutical Representative, a typical day might include the following:</strong></p><ul><li><p>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.</p></li><li><p>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</p></li><li><p>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</p></li><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</p></li><li><p>Leverage all communication channels including digital channels, 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 Immunology leadership team</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</p></li><li><p>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</p></li><li><p>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</p></li><li><p>You can operate effectively in a “start-up” model as this is a completely new team.</p></li></ul><p>To be considered for this opportunity you must hold a Carte Professionnelle with minimum <strong>5+ years of pharmaceutical sales experience in Oncology</strong>. You are happy with regular travel and have a valid driver's license. Conversational English would be desirable, but not required.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 03:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Wednesday - Saturday 2nd Shift]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45541]]></requisitionid>
    <referencenumber><![CDATA[R45541]]></referencenumber>
    <apijobid><![CDATA[r45541]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45541/calibration-technician-wednesday-saturday-2nd-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[<div><div>We are currently looking to add a Calibration Technician to our growing team, working a Wednesday - Saturday 2pm – 12:30am shift. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</div></div><div><div><div><div><p><strong>Please note training will take place Monday-Friday 8:00am-4:30pm for approximately 6 months. Working hours thereafter will be Wednesday-Saturday 2pm-12:30am. </strong><strong>Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Calibration Technician, a typical day might include the following:</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></ul><h3>This role might be for you if you:</h3><ul><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>Seek to build and maintain positive working relationships with the business</li><li>Possess strong written and verbal communication skills</li><li>Maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p>To be considered for the Calibration Technician position you must be willing and able to work a Wednesday - Saturday 2pm-12:30am schedule. 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><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>#REGENTOSK </p></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 (hourly)</strong></strong></p>$28.46 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Tuesday-Saturday 3rd Shift]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45542]]></requisitionid>
    <referencenumber><![CDATA[R45542]]></referencenumber>
    <apijobid><![CDATA[r45542]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45542/calibration-technician-tuesday-saturday-3rd-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>We are currently looking to add a Calibration Technician to our growing team, working a Tuesday-Saturday 10:00pm – 8:30am shift. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</p><p><strong>Please note training will take place Monday-Friday 8:00am-4:30pm for approximately 6 months. Working hours thereafter will be Tuesday-Saturday 10:00pm-8:30am. </strong><strong>Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Calibration Technician, a typical day might include the following:</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></ul><h3>This role might be for you if you:</h3><ul><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>Seek to build and maintain positive working relationships with the business</li><li>Possess strong written and verbal communication skills</li><li>Maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p>To be considered for the Calibration Technician position you must be willing and able to work a Tuesday-Saturday 10:00pm – 8:30am schedule. 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><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>#REGENTOSK </p><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 (hourly)</strong></strong></p>$28.46 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Digital Transformation Operations Lead]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45895]]></requisitionid>
    <referencenumber><![CDATA[R45895]]></referencenumber>
    <apijobid><![CDATA[r45895]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45895/senior-director-digital-transformation-operations-lead/]]></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>Regeneron is seeking a Senior Director, Digital Transformation Operations Lead to join our Global Development organization.</p><p><strong>In this role, a typical day might include:</strong></p><p>Global Development is embarking on a Digital Transformation (DT) project that will incorporate AI, machine learning, and automation into our processes to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. This position will develop strategy and lead project management for Digital Transformation and will work with a wide array of stakeholders to make sure that changes to technology and processes are implemented with their maximum impact. This position’s remit spans Global Development (GD), including development operations, regulatory, medical affairs, and Regeneron’s clinical development units. While mainly focusing on operations, this position will also be expected to contribute to overall strategy, including prioritization and alignment with other Regeneron business units outside of Global Development. This position will also help translate and represent the work of technical groups that will be developing and implementing platforms, algorithms, and systems as part of the digital transformation project. This position will most likely also be the key point of contact between the DT team and outside strategic consultants who will be advising GD on executing digital transformation.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Work with DTI and GD leadership to develop and drive the strategic vision for the overall DT project</p></li><li><p>Lead cross-functional collaboration with internal teams, including AI leads, advanced informatics, IT, and other technical groups, to develop and implement cutting-edge solutions.</p></li><li><p>Act as the primary liaison between GD and external strategic consultants, ensuring alignment on priorities, use case validation, and change management initiatives.</p></li><li><p>Tailor DT strategy to Global Development’s needs and priorities, translating these priorities into specific project plans</p></li><li><p>Build and manage relationships with external partners and vendors, ensuring alignment with business objectives and delivery of high-quality outcomes. Co-lead the development and execution of a robust change management strategy to ensure successful adoption of new processes, technologies, and ways of working.</p></li><li><p>Foster a culture of innovation and adaptability, empowering teams to embrace digital transformation.</p></li><li><p>Oversee the development of comprehensive project plans, outlining prioritization frameworks, technical implementation strategies, and risk mitigation approaches.</p></li><li><p>Establish and monitor performance metrics (KPIs) to evaluate project success, delivering regular updates and strategic recommendations to executive leadership.</p></li><li><p>Coordinate DT strategy and initiatives with other Regeneron business units (e.g., Commercial, Research) to drive enterprise-wide synergies and maximize impact.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum BS with 15+ years of relevant experience (or MS/MBA with 13+ years of relevant experience)</p></li><li><p>At least 7 years experience developing and leading strategy, including accountability for the success of the implementation, in life sciences or healthcare.</p></li><li><p>Experience leading and implementing major strategic projects in the life sciences or healthcare setting</p></li><li><p>Robust knowledge of the essential processes involved in pharmaceutical R&D with a focus on the drug development lifecycle (e.g. protocol and trial design, safety reporting, outcomes research, etc.)</p></li><li><p>Robust technical knowledge of AI/ML and relevant platforms and technologies as well as common enterprise systems</p></li><li><p>Experience presenting to and educating senior leadership around the fundamentals of digital transformation including investment, go/no go decisions, especially with non-technical audiences</p></li><li><p>Excellent communication, stakeholder management, change management, and strategic planning skills</p></li><li><p> Proven ability to work in a matrixed organization, developing and leading complex projects with multiple stakeholders while developing a network of subject matter experts</p></li><li><p>May require travel up to 20%</p></li></ul><p>#GDDOPMJobs</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>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Field Medical Affairs- Oncology (northern CA, Nevada)]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45432]]></requisitionid>
    <referencenumber><![CDATA[R45432]]></referencenumber>
    <apijobid><![CDATA[r45432]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45432/associate-director-field-medical-affairs-oncology-northern-ca-nevada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[San Jose]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs you will engage in scientific exchange and collaborate with Oncology disease experts and product information as well as research initiatives. We provide scientific and/or medical expertise by thoroughly understanding Oncology as a therapeutic area serving as a scientific/medical resource. We present scientific and clinical data and disease state awareness in response to requests for information to therapeutic area specialists, practitioners, investigators, research coordinators, site personnel and internal partners.</p><p><strong>Territory: </strong>northern California and Nevada</p><p><strong>A typical day may include the following</strong><br>• Identifies and maintains a list of relevant medical/therapeutic area professionals, investigator targets and associated plans of action.<br>• Participates in the development and management of clinical trials.<br>• Review of concept proposals and development of protocols<br>• Identifies and assists in selection of investigators and trial sites<br>• Supports site initiation and enrollment activities<br>• Acts as a resource for area healthcare professionals within the surrounding trial site community<br>• Collaborates with Clinical Development and other trial staff to implement plans and strategies. <br>• Establishing scientific relationship with investigators and Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifies gaps in research needs of company and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Performs disease education with identified practitioners, payers and researchers.<br>• Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence<br>• Assists with management of clinical data to ensure rapid and accurate communication of scientific/clinical results supporting abstract, poster, presentation, and manuscript development.</p><p><strong>This may be for you if you:</strong><br>• Enjoy working independently in the field, while having an impact on the company’s mission.<br>• Are passionate about developing knowledge of and sharing clinical scientific data<br>• Like working corroboratively and developing relationships in academic and clinical practice settings<br>• Have the highly developed ability to balance and prioritize multiple initiatives and excel while implementing them independently</p><p>To be considered for this an advanced Clinical/Science Degree required (MD, PharmD, PhD) is required. A minimum of 5 years related work experience in Oncology as a Field Medical Affairs representative or Medical Science Liaison required. Residence must be within the assigned territory. </p><p>#msl #medicalscienceliaison</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 16:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager – Regulatory Submission Compliance]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45206]]></requisitionid>
    <referencenumber><![CDATA[R45206]]></referencenumber>
    <apijobid><![CDATA[r45206]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45206/senior-manager-regulatory-submission-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>The Senior Manager— CMC Regulatory Submission Compliance is responsible for aligning the regulatory landscape with country-specific requirements and supporting clinical regulatory submission activities, supply planning, and QP certification. This role leads processes and cross-functional coordination, ensuring high-quality documentation and timely approvals for clinical and commercial activities.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Provide support for the management of the regulatory submission form process, reviewing clinical regulatory documentation submitted to global health authorities to enable lot release for clinical trials and commercial markets.</p></li><li><p>Lead and coordinate the pre-submission review process to ensure CMC regulatory documentation aligns with global requirements and country-specific expectations.</p></li><li><p>Participate in cross-functional meetings to identify CMC regulatory issues related to submission documentation; ensure clear communication between IOPS and global development on submission-related risks.</p></li><li><p>Develop and improve procedures and systems for review and feedback on the CMC global clinical regulatory submission packages, approvals, and status updates to improve visibility and efficiency.</p></li><li><p>Lead meetings and presentations on complex regulatory issues; contribute to and build regulatory justifications to support filings.</p></li><li><p>Provide CMC regulatory submission oversight of CRO activities, ensuring deliverables meet compliance standards and timelines.</p></li><li><p>Keep management and collaborators advised of assessments, overall strategy, and project status through structured reporting and updates.</p></li><li><p>Implement comprehensive training, tools, and reporting metrics for senior management to strengthen submission compliance and operational readiness.</p></li><li><p>Act as a submission compliance liaison with Regulatory Affairs, Regulatory Submission Management, Clinical Drug Supply and Logistics, and Quality to ensure submissions appropriately support the release of investigational product.</p></li><li><p>Support activities by ensuring documentation completeness and compliance.</p></li><li><p>Mentor, coach, and, where applicable, manage direct reports to develop regulatory capabilities and consistent practices.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><p>A Bachelor’s degree in Chemistry, Biology, or a related field; advanced qualifications or program management experience are a plus. 8+ years of experience in the biotech or pharmaceutical industry, including a minimum of 2 years of relevant CMC experience.</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>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 05:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Compliance Reporting - US Transparency]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45851]]></requisitionid>
    <referencenumber><![CDATA[R45851]]></referencenumber>
    <apijobid><![CDATA[r45851]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45851/associate-director-compliance-reporting-us-transparency/]]></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>Position Title:</strong><br>Associate Director, Compliance Reporting (US Transparency)</p><p><strong>Location:</strong><br>Sleepy Hollow, NY</p><p><strong>Department:</strong><br>Corporate Compliance</p><p><strong>Reports To:</strong><br>Director, Compliance Reporting</p><p><strong>Overview</strong><br>The Associate Director, Compliance Reporting leads data collection, aggregation, analysis, and reporting for Regeneron’s US Transparency Program (Federal Open Payments and US State reporting). Serving as a subject matter expert on federal and state aggregate spend regulations, this role partners cross-functionally to ensure accurate, timely, and compliant reporting, while driving process excellence, operational rigor, and continuous improvement across systems, policies, and training.</p><p><strong>Key Responsibilities</strong></p><ul><li>Act as a subject matter expert on US transparency and aggregate spend requirements, providing practical guidance to internal stakeholders.</li><li>Serve as a trusted advisor to resolve system, process, and policy questions; coordinate with cross-functional partners to triage and resolve issues.</li><li>Lead the development, implementation, and continuous improvement of policies, work instructions, and controls governing HCP/HCO spend capture, validation, and reporting.</li><li>Design and deliver training and ongoing education to internal teams on requirements, systems, and processes to drive adoption and adherence.</li><li>Own end-to-end data operations: collect, aggregate, research, validate, and reconcile HCP/HCO spend data to meet federal and state reporting obligations.</li><li>Use metrics and dashboards to monitor data quality, identify trends and outliers, and proactively implement corrective and preventive actions.</li><li>Stay current on internal policy updates and external regulatory changes; translate requirements into operational updates and change management plans.</li><li>Ensure robust documentation, audit trails, and records retention to support transparency reporting and team operations.</li><li>Triage, document, and escalate compliance concerns when appropriate; contribute to investigations and remediation plans.</li><li>Participate in industry trainings; disseminate insights and best practices to elevate team capabilities.</li><li>Collaborate closely with cross-functional stakeholders to track reportable spend and ensure complete, accurate submissions under applicable US state and federal transparency laws.</li></ul><p><strong>Minimum Qualifications</strong></p><ul><li>Bachelor’s degree</li><li>10+ years of experience in accounting, finance, or compliance within the pharmaceutical/life sciences industry.</li><li>Thorough knowledge of federal and state aggregate spend regulations and hands-on experience preparing and submitting reports and working in a transparency disclosure system.</li><li>Proficiency with Microsoft Excel, Word, PowerPoint, and SharePoint; strong data validation, reconciliation, and documentation skills.</li><li>Proven ability to operate in a fast-paced environment and deliver against reporting deadlines.</li><li>Strong collaboration skills with the ability to work independently and as part of a broader team.</li><li>High sense of urgency, ownership, and attention to detail; excellent written and verbal communication.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 13:56:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Spain]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46238]]></requisitionid>
    <referencenumber><![CDATA[R46238]]></referencenumber>
    <apijobid><![CDATA[r46238]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46238/associate-director-finance-administration-spain/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></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>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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Quality Control Scientist]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45796]]></requisitionid>
    <referencenumber><![CDATA[R45796]]></referencenumber>
    <apijobid><![CDATA[r45796]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45796/sr-quality-control-scientist/]]></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 looking for a Sr Quality Control Scientist in the Technical Resources Department. This position performs assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.</p><p>As a Sr QC Scientist for Chemistry in the Technical Resources Department, a typical day might include the following:</p><ul><li><p>Performs assay development/validation for QC.</p></li><li><p>Reviews new test procedures and assays.</p></li><li><p>Evaluates and bring in new methodologies/techniques when needed.</p></li><li><p>Facilitate assay transfer from R&D and to business partners</p></li><li><p>Organize analytical assay transfer internally and externally.</p></li><li><p>Set product specification.</p></li><li><p>Participates in technical troubleshooting and problem investigation.</p></li><li><p>Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.</p></li><li><p>Participates in training programs for analysts.</p></li></ul><p>This job might be for you if:</p><ul><li>You have experience in drug product functional and dimensional testing, as well as visual inspection.</li><li>You like dealing with technical issues, troubleshooting, and constant change</li><li>You are a team player who can work with a variety of different people on different tasks</li><li>You have strong written and verbal communication skills</li><li>You enjoy mentoring and training others on systems, processes and problem solving</li><li>You enjoy working in a fast-paced environment and are flexible to changing requirements</li><li>You can take on new and sometimes ambiguous challenges and learn quickly</li></ul><p>To be considered for a Sr QC Scientist role you must have a BS in Chemistry, or Engineering, and 6+ years of relevant experience. Higher level degree preferred.</p><p>Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred.</p><p>Level is determined based on experience relevant to the role.</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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 14:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46313]]></requisitionid>
    <referencenumber><![CDATA[R46313]]></referencenumber>
    <apijobid><![CDATA[r46313]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46313/manager-clinical-scientist-hematology/]]></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 Manager, Clinical Sciences, Hematology leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p>As a Manager, a typical day may include the following:</p><ul><li><p>Member of the Clinical Study Team and Global Clinical sub-team</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>Develops/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>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late-stage assets</p></li><li><p>Assists with development of the Expanded Synopsis and may author clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Contributes to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority). Presents data and information to external investigators (SIV) and internal collaborators</p></li></ul><p>This role may be for you if:</p><ul><li><p>Possess demonstrated knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrate solid medical writing skills</p></li><li><p>Proven ability to influence within team and may influence across functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li></ul><p>To be considered for this position, you must have a minimum of Bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). We are seeking ≥ a minimum of 3 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. You have a basic knowledge of oncology or hematology therapeutic areas as well as a proven track in clinical trial process improvements. We need an individual with demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Resolves novel problems requiring creative application of advanced skill, training, and education.</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Process Validation Oversight]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43170]]></requisitionid>
    <referencenumber><![CDATA[R43170]]></referencenumber>
    <apijobid><![CDATA[r43170]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43170/manager-process-validation-oversight/]]></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><div><div><div><p>Regeneron is hiring a Manager, Process Validation Oversight to lead a team dedicated to ensuring the integrity of our process validation processes. This role is integral in supporting process validation activities, ensuring global consistency, addressing recurring themes in process documentation, and playing a pivotal role in regulatory inspections and compliance. </p></div><div></div><div><p>In this role, a typical day might include the following: </p></div><div><ul><li><p>Ensuring alignment between validation activities and Process Sciences initiatives to support successful transition of processes from development to manufacturing. </p></li></ul></div><div><ul><li><p>Collaborate closely with internal Process Sciences team to provide technical expertise and ensure consistency in Process Validation strategies. </p></li></ul></div><div><ul><li><p>Presenting/defending validation strategies, documentation, and processes to FDA and other regulatory agencies. </p></li></ul></div><div><ul><li><p>Reviewing and approving process validation documents, procedures, and protocols, proposing modifications and corrections where necessary to meet regulatory requirements and expectations. </p></li></ul></div><div><ul><li><p>Overseeing all aspects of QA Validation including review and approval of failure investigations, change controls, SOPs, Validation protocols and summary reports, and validation master plans. </p></li></ul></div><div><ul><li><p>Conduct one-on-one discussions with team members to review their performance feedback and set development goals, fostering professional growth within the team. </p></li></ul></div><div></div><div><p>This role might be a for you if you: </p></div><div><ul><li><p>Bring hands-on validation experience in a GMP-regulated environment. </p></li></ul></div><div><ul><li><p>Possess deep understanding and expertise in Process Validation. </p></li></ul></div><div><ul><li><p>Enjoy building strong, collaborative relationships across global internal teams. </p></li></ul></div><div><ul><li><p>Have a continuous improvement mindset. </p></li></ul></div><div><ul><li><p>Are an experienced leader who inspires and guides a multi-tiered team. </p></li></ul></div><div></div><div><p>To be considered for this role, you must hold a Bachelor’s degree in Engineering, Chemistry, or Life Sciences degree and the following minimum years of experience for each level: </p></div><div><ul><li><p>Associate Manager: 6+ years </p></li></ul></div></div><div><div><ul><li><p>Manager: 7+ years </p></li></ul></div><div></div><div><p>May substitute relevant experience in lieu of education requirement. Level is determined on qualifications relevant to the role. </p></div><div></div><div><p>#REGNQA </p></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>$90,800.00 - $173,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Wed, 17 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43877]]></requisitionid>
    <referencenumber><![CDATA[R43877]]></referencenumber>
    <apijobid><![CDATA[r43877]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43877/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>A Sr. Manager provides timely support to the project team on all programming matters according to the project strategies within a therapeutic area. As an integral part of a project team, the incumbent provides project leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical Analysis Plan, programming specifications or user requirements/design documents using internal standards and guidelines. The incumbent is responsible for leading the programming aspect of the project, both internally or CROs, for all programming deliverables and participates in the identification and development of programming standards and macro development to facilitate the creation of statistical deliverables from a single study through to regulatory approval, product launch, and annual reports. May be asked to oversee special projects / work with clinical task force. Meets statistical adhoc requests of senior management.</p><p><br><strong>As a Senior Manager, A typical day may include:</strong></p><p><br>• Independently coordinate and oversee the preparation, execution, reporting and documentation of project analysis programming within a therapeutic area using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Manage and coordinate programming and QC of analysis datasets and TFLs following Regeneron standard data models and/o integration of data across studies in support of CSS/CSE and esub deliverables.<br>• Implement and mentor others on the use of department standardization tools or therapeutic area standard analysis when programming clinical data or system application deliverables.<br>• Contribute to programming development and quality control of the programming deliverables utilizing Regeneron tools and methodologies.<br>• Programming representative within a therapeutic area in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, programming representative for an application development to the user audience.<br>• Develop data models, programming standards and code, and training end users in the use of project standards to support programming deliverables that follow regulatory submission requirements.<br>• Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.<br>• Advises all relevant employees about the procedures surrounding retention of data, records, and information for employees in their group.</p><p><strong>To be considered for this role, you must meet the following requirements</strong>:<br>Education<br>• Masters Degree<br>• SAS Certification desirable.</p><p>Experience<br>• 8 – 10 Years</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Legal Data Privacy Operations]]></title>
    <date><![CDATA[Thu, 18 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43971]]></requisitionid>
    <referencenumber><![CDATA[R43971]]></referencenumber>
    <apijobid><![CDATA[r43971]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43971/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>Regeneron is seeking a dynamic and forward-thinking Legal Privacy Manager to manage our privacy program operations while driving and implementing strategic transformation within the Law Dept. / Privacy Office. This individual will bring a unique blend of innovative thinking, business strategy expertise, and operational excellence to enhance our privacy program through technology-driven solutions and process optimization. As a key member of the Privacy Office within Regeneron’s Law Department, you will have an important role in advancing our data privacy program. This includes managing complex privacy projects, delivering tactical operational support, and supporting governance initiatives. The ideal candidate is strategic, but also capable of rolling up their sleeves to manage day-to-day operations and implement impactful solutions.</p><p><em><strong>Th</strong></em><em><strong><em><strong>is </strong></em>role will require 4 days per week onsite at our Global HQ Campus in Sleepy Hollow, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong><em>A typical day might include:</em></strong></p><ul><li>Identifying opportunities for digital transformation in privacy operations and managing their implementation including incorporating emerging technologies and innovative solutions.</li><li>Managing timelines, deliverables, and metrics of multiple ongoing privacy related projects to ensure timely and compliant execution.</li><li>Triaging and overseeing privacy requests to ensure efficient resolution of issues.</li><li>Documenting advice and implementation of online privacy notices and controls, tracking technologies, and privacy-enhancing tools.</li><li>Conducting privacy risk assessments, maintaining records of processing activities and managing individual rights request processes.</li><li>Developing and maintaining privacy program metrics and KPIs.</li><li>Upkeep and development of internal policies, procedures, guidance documents, training and awareness, including our Intranet site.</li><li>Managing and preparing for our Data Privacy Steering Committee meetings, including coordinating meetings, developing presentations and handling minutes.</li><li>Coordinate and facilitate Privacy Steward engagement to advance enterprise-wide privacy initiatives, ensuring alignment with organizational objectives and regulatory requirements.</li><li>Managing vendor relationships by overseeing the execution of Statements of Work and ensuring timely processing of requisitions, purchase orders, and invoices.</li></ul><p><strong>Required</strong>:</p><ul><li>BS/BA Degree</li><li>At least 5 years of experience in privacy or a related field</li><li>Strong project management skills and ability to manage multiple priorities and deliverables simultaneously</li><li>Excellent relationship building skills and demonstrated ability to work collaboratively</li><li>Exceptional oral, written, and presentation communication skills</li><li>AI literacy (experience with digital transformation helpful)</li></ul><p><strong>Preferred</strong>:</p><ul><li>Knowledge of privacy laws and understanding of privacy risk management technologies</li><li>Certified Information Privacy Manager (CIPM) or Certified Information Privacy Technologist (CIPT) Project Management Professional (PMP) or equivalent certification</li><li>Advanced degree in a related field</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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Enterprise Platform Product Owner - Office of the Chief Information Officer (OCIO)]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44163]]></requisitionid>
    <referencenumber><![CDATA[R44163]]></referencenumber>
    <apijobid><![CDATA[r44163]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44163/associate-manager-enterprise-platform-product-owner-office-of-the-chief-information-officer-ocio/]]></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><div><p>Are you passionate about driving enterprise platform strategies and delivering impactful solutions in the biotech industry? This role is designed for an experienced product owner with relevant pharmaceutical/biotech experience in disciplines including Project Portfolio Management (PPM), Technology Business Management (TBM), financial-based systems, and enterprise architecture. The candidate should also possess a proven ability to lead cross-functional teams, manage technical upgrades, oversee financial and resource management, collaborate with stakeholders, and craft compelling narratives for senior executives to realize business outcomes from digital technology platforms and investments. </p><p><strong>A typical day might include the following:</strong></p></div><div><ul><li><p>Define and maintain the product vision, strategy, and roadmap for enterprise platforms, with a focus on PPM, TBM, and financial-based systems. </p></li></ul></div><div><ul><li><p>Lead the creation of product roadmap presentations for steering committees and senior leadership, ensuring alignment with organizational goals. </p></li></ul></div><div><ul><li><p>Collaborate with business stakeholders to understand their needs, prioritize features, and ensure platform capabilities deliver measurable value. </p></li></ul></div><div><ul><li><p>Act as the primary liaison between business teams, IT teams, vendors, third-party and internal helpdesks to gather requirements and ensure alignment. </p></li></ul></div><div><ul><li><p>Facilitate workshops, discovery sessions, and regular communication with stakeholders to prioritize features and resolve challenges. </p></li></ul></div><div><ul><li><p>Leverage expertise in PPM tools (e.g., Planview, Jira, Project Place, MS Project and others) to optimize project and portfolio management processes. </p></li></ul></div><div><ul><li><p>Oversee the implementation and integration of TBM frameworks (e.g., Apptio, ServiceNow, Oracle) to enhance IT financial management, cost transparency, and value optimization. </p></li></ul></div><div><ul><li><p>Ensure financial-based systems (e.g., Oracle ERP, budgeting, forecasting) are seamlessly integrated with PPM and TBM platforms to enable comprehensive reporting and analytics. </p></li></ul></div><div><ul></ul></div></div><div><div><ul><li><p>Ensure platform design and architecture align with enterprise standards, scalability, and security requirements. </p></li></ul></div><div><ul><li><p>Lead the development of architecture documents for review and approval by enterprise architecture and governance teams. </p></li></ul></div><div><ul><li><p>Provide oversight of platform services through the helpdesk, ensuring timely resolution of issues and optimal user satisfaction. </p></li></ul></div><div><ul><li><p>Manage service-related contracts, ensuring compliance, performance, and alignment with organizational goals. </p></li></ul></div><div><ul><li><p>Track and analyze day-to-day metrics to monitor platform performance and identify areas for improvement.</p></li></ul></div><div><ul></ul></div><div><ul><li><p>Manage and oversee technical upgrades for enterprise platforms, ensuring minimal disruption to business operations. </p></li></ul></div></div><div><div><ul><li><p>Work closely with finance partners to articulate the financial impact of platform investments and ensure alignment with business objectives. </p></li></ul></div><div><p><strong>This role might be for you if you:</strong></p><div><div><ul><li><p>Strong knowledge of PPM tools (e.g., Planview, Project Place, Jira, Microsoft Project) and TBM solutions (e.g., Apptio, ServiceNow TBM). </p></li></ul></div><div><ul><li><p>Experience with enterprise architecture principles and system integration strategies. </p></li></ul></div><div><ul><li><p>Knowledge of financial-based systems (e.g., Oracle, Workday) and their integration with TBM frameworks. </p></li></ul></div><div><ul><li><p>Proven ability to manage complex, cross-functional projects and deliver results in a fast-paced environment. </p></li></ul></div><div><ul><li><p>Strong analytical skills, with the ability to translate business needs into technical requirements. </p></li></ul></div><div><ul><li><p>Exceptional storytelling and interpersonal skills, with experience preparing executive-level presentations that are clear, concise, and impactful. </p></li></ul></div><div><ul><li><p>Experience in data governance, financial reporting, and compliance </p></li></ul></div></div><div><div></div></div><p><strong>To be considered for this role</strong>, <strong>you must have</strong><strong>:</strong></p><ul><li><p>Bachelor’s degree in Computer Science, Information Systems, Business Administration, or a related field (Master’s degree preferred). </p></li></ul></div><div><ul><li><p>7+ years of experience in product ownership or management roles, with a focus on enterprise platforms, PPM tools, TBM frameworks, and financial-based systems. </p></li><li><p>Product Owner (CSPO) or similar Agile certification (preferred)</p></li><li><p>TBM certifications (e.g., Apptio TBM Unified Certification) are highly desirable.</p></li><li><p>PMP, SAFe Agile, or ITIL certifications are a plus.</p></li></ul></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>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Product Testing and Release Management Lead (Oracle)]]></title>
    <date><![CDATA[Thu, 18 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44209]]></requisitionid>
    <referencenumber><![CDATA[R44209]]></referencenumber>
    <apijobid><![CDATA[r44209]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44209/director-erp-product-testing-and-release-management-lead-oracle/]]></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 Oracle Fusion ERP Product Testing and Release Management Lead governs testing and release activities for the Oracle Fusion Cloud implementation. The role focuses on quarterly Oracle patch impact analysis, regression testing, controlled release cycles, and system stability across phased deployments. This position works closely with the Testing (MTS) team, SI partners, GPOs, Product Leads, QA/CSV, and Oracle to ensure consistent testing standards, effective use of automated testing tools, robust test documentation in Jira, and compliance with Regeneron’s validation, SOX, and data integrity requirements.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Partner with the Testing (MTS) team to plan, coordinate, and execute regression testing—including preparation and maintenance of test scripts, test scenarios, regression libraries, and automation for quarterly Oracle updates.</p></li><li><p>Use enterprise automation tools (e.g., Tosca or equivalent) to build and maintain automated regression test suites across Oracle ERP Cloud and integrations with boundary applications.</p></li><li><p>Oversee the use of Jira for managing test scripts, test scenarios, execution tracking, defect logging, triage, and reporting.</p></li><li><p>Lead testing governance across Regression, Integration SIT, UAT, and release readiness cycles.</p></li><li><p>Review Oracle quarterly patch release notes, perform impact assessment, and identify functional or technical areas requiring testing or remediation.</p></li><li><p>Maintain a risk-based regression testing strategy aligned with Oracle’s patch cadence and program release cycles.</p></li><li><p>Coordinate with SI partners to ensure all testing deliverables (scripts, scenarios, data, traceability matrices) meet Regeneron’s standards and are updated in Jira.</p></li><li><p>Collaborate with GPOs, Product Leads, and SMEs to ensure comprehensive cross-functional end-to-end test coverage.</p></li></ul><p><strong>This Job Might Be For You If You Have:</strong></p><ul><li><p>Expertise in analyzing Oracle Fusion Cloud quarterly updates and identifying system impacts.</p></li><li><p>Ability to interpret release notes and convert them into actionable testing scope.</p></li><li><p>Experience with automated testing tools such as Tosca, Selenium, or similar, especially for Oracle Cloud regression automation.</p></li><li><p>Strong understanding of ERP testing processes across Regression, SIT, UAT, and validation cycles.</p></li><li><p>Proficiency with Jira for managing test scripts, test scenarios, execution cycles, and defect tracking.</p></li><li><p>Solid grounding in SOX, GxP, data integrity, validation, and audit readiness.</p></li></ul><br><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Bachelor’s degree in Computer Science, Information Systems, Engineering, or a related field.</p></li><li><p>15+ years of experience in Oracle ERP applications testing, quality assurance, or release management.</p></li><li><p>10+ years of experience specifically with Oracle Fusion Cloud testing and release management.</p></li><li><p>Experience with Oracle Fusion Cloud or Oracle EBS release cycles and quarterly update impact analysis.</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[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Infrastructure Engineer]]></title>
    <date><![CDATA[Wed, 04 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44776]]></requisitionid>
    <referencenumber><![CDATA[R44776]]></referencenumber>
    <apijobid><![CDATA[r44776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44776/automation-infrastructure-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Automation Infrastructure Engineer who will be responsible for delivering and maintaining automation-based systems and solutions which provide for flexible, innovative, cost effective, compliant and quality-focused manufacturing of Biopharmaceuticals. </p><p><strong>As an Automation Infrastructure Engineer, a typical day might include the following:</strong></p><ul><li>Supporting critical-to-manufacturing systems and ensuring their high availability reducing or eliminating unplanned downtime</li><li>Designing, configuring, programming, and qualifying Rockwell FactoryTalk Systems (DCS), ThinManager; Asset Centre</li><li>Excellent understanding of protocols such as OPC, UPC-UA, MQTT, TCP/IP, HTTP</li><li>Ensuring appropriate monitoring, alerting and response to network, system and application issues affecting functionality and availability</li><li>Providing automation technical knowledge and support for troubleshooting, investigations, installations and training</li><li>Providing automation system design for data integrity, stability, and integration between different systems</li><li>Designing and delivering end-to-end data solutions to meet current and future needs</li><li>Facilitating the smooth transition of projects from Development into Production Environment</li><li>Overseeing migration of data from legacy systems to new applications</li><li>Acting as a Subject Matter Expert and the technical go-to for Historian and data integration solutions</li><li>Ensuring compliance and optimisation of automation systems</li><li>Creating, modifying, and maintaining automation systems and documentation, including automation specification documents and SOPs, in a compliant state</li><li>Working closely with the corporate IT infrastructure team to ensure continued technical alignment. Managing support for manufacturing dependencies and touchpoints with enterprise systems</li><li>Supporting the validation of automation systems with QA Validation</li><li>Designing and implementing solutions across automation platforms in line with the site change control procedures</li><li>Implementing and reporting of preventative maintenance, patching & upgrades</li><li>Developing a plan for system obsolescence, vendor support and upgrade scheduling</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have some experience with cGMP and validation pertaining to biopharmaceutical production operations and computerised systems and the ability to implement best practices (GAMP) to ensure site automation systems are cGMP compliant</li><li>Have an understanding of automation system implementation and validation life cycle along with an understanding of the product quality impact of changes</li><li>Demonstrated capability for leading complex projects technically from initial design / development through to the validation of the facility in support of defined objectives</li><li>Experience of implementing change controls and investigating system deviations/events</li><li>Experience with SQL databases</li><li>Experience with networking: Cisco, Stratix Switches, Firewalls</li><li>Experience with Enterprise Security: Antivirus and network security</li><li>Experience with monitoring and security tools such as Splunk</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better</li></ul><p>To be considered for this position you should have a Bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level:</p><ul><li>Engineer: 2+ years</li><li>Senior Engineer: 5+ years</li><li>Principal Engineer: 8+ years</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>#IRELIM #JOBSIEPR #LI-Onsite #REGNIRLTO</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Feb 2026 04:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[District Sales Manager - Dermatology-Tri-State (NY, CT, NJ)]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44939]]></requisitionid>
    <referencenumber><![CDATA[R44939]]></referencenumber>
    <apijobid><![CDATA[r44939]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44939/district-sales-manager-dermatology-tri-state-ny-ct-nj/]]></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>Geography: Wayne, NJ; Bronx, White Plains, Syracuse, Buffalo, CT</strong></p><p><strong>District Manager, Tri-State (NY, CT, NJ) - Dermatology</strong></p><p>The District Manager (DM), Dermatology will report to the Regional Director, Dermatology and be responsible for hiring, leading, developing and retaining the Dermatology Medical Specialists in their assigned district. </p><p><strong>A Typical Might Look Like This:</strong></p><p>The DM 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 Dermatology District assigned. The DM will work closely with their Alliance partner counterpart(s) to insure full cooperation and transparency. The DM will work closely to ensure appropriate development and retention of key personnel within the district to continue to facilitate growth in the commercial organization. The DM 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>This Position Might Be for You If:</strong></p><ul><li><p>Successful leadership record of hiring, coaching, developing, promoting, and retaining top talent within span of control and ability to effectively manage performance of the team.</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a District Sales Manager in complex markets within complex systems required.</p></li><li><p>Strong understanding of Payer environment, reimbursement and challenges within National, Regional and local payer market including; government programs, managed health care and evolving health care systems.</p></li><li><p>Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners.</p></li></ul><p>To be considered for this opportunity you will have the following: Bachelor’s degree required, Master’s degree or other advanced education/certifications a plus (Focused degree in science or clinical experience is a plus). Minimum of 7 years of pharmaceutical/biopharmaceutical experience with 3 years of sales leadership/management in office-based, sub-cutaneous self-injectable biologic markets required. Experience in the Dermatology market preferred. Ability to travel extensively with local and regional influence.</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>$175,300.00 - $218,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Brooklyn, NY]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45007]]></requisitionid>
    <referencenumber><![CDATA[R45007]]></referencenumber>
    <apijobid><![CDATA[r45007]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45007/medical-specialist-i-dermatology-brooklyn-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Brooklyn]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Brooklyn, NY</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Global Development Quality Assurance (GLP)]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45122]]></requisitionid>
    <referencenumber><![CDATA[R45122]]></referencenumber>
    <apijobid><![CDATA[r45122]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45122/senior-director-global-development-quality-assurance-glp/]]></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>As a Senior Director, Global Development Quality Assurance (GDQA) you will provide leadership for an entire GLP function. You will lead all staff while developing and leading all aspects of the execution of functional/departmental mission and vision. You will create and oversee strategic partnerships and implement risk-based quality auditing activities internally and with external organizations. You are expect to apply your expert knowledge of the FDA and EU regulations and ICH guidance documents with other regulations affecting drug development. </p><p>You will manage Good Laboratory (GLP) audit function within GDQA. In addition, we partner with other members of the GDQA, identifying trends through metrics to diagnose and remediate systemic quality issues. We oversee the development, execution and reporting of the overall GxP Audit Program(s) for which they are responsible. </p><p>This position will be on-site 4 days/week at our Tarrytown, NY offices. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following</strong>: <br>• Developing and managing the overall strategic plan for the GLP audit functions. <br>• Represent the GDQA audit function by providing audit and compliance input in cross functional meetings and external meetings. <br>• Manage, hire and develop direct reports within GDQA and conducting Mid-year and End-of year performance assessments. <br>• Lead the identification of internal quality/compliance issues and act as a catalyst for process improvements to promote standardization and best practices. <br>• Represent GDQA on top priority teams, complex compliance projects and initiatives both within and across functional areas or other departments as applicable. <br>• Be responsible for policies, standards, and regulations, and evaluate potentially critical problems. <br>• Oversee the education and/or training of the GDQA organization and other Global Development departments as needed. <br>• Ensure succession planning and business continuity for GDQA department.</p><p><strong>This may be for you if you: </strong><br>• Can demonstrate success in leading a GLP Quality Assurance (GDQA) function. <br>• Self-motivated with the ability to work effectively in a dynamic environment with ambiguity <br>• Ability to effectively manage multiple priorities with a sense of urgency <br>• Strong people and project management, collaboration skills and negotiation of complex situations </p><p>To be considered a Bachelor’s degree (Master’s preferred) with 12+ years of relevant industry experience is required. We are seeking a minimum of 10 years’ experience working in GLP auditing and/or audit strategy and 6-8 years prior supervisory/leadership experience. Strong knowledge of FDA or other Regulatory Inspections of Investigator sites, Sponsors or CROs is necessary. Demonstrated experience in driving Quality into the Clinical Trial Operations processes. <br> </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>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, QA Investigations]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43314]]></requisitionid>
    <referencenumber><![CDATA[R43314]]></referencenumber>
    <apijobid><![CDATA[r43314]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43314/associate-manager-qa-investigations/]]></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 fill an Associate Manager, QA Investigations position. This position is responsible for providing oversight of the quality review, quality approval and management of deviation events, investigations and CAPA.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Manages a team with direct oversight of review and approval for deviations, laboratory investigations and corrective actions.</p></li><li><p>May review, verify and approve system records.</p></li><li><p>Collaborates across QA to provide succinct support to investigation teams to drive quality outcomes.</p></li><li><p>Approves and reviews SOP revisions.</p></li><li><p>Provides direction for cross-functional study team meetings and interacts with subject matter authorities.</p></li><li><p>Provides input for error prevention and corrective actions based on investigational findings.</p></li><li><p>Involved in post-production management of events as required to facilitate closures to meet the required timelines.</p></li><li><p>Serves as a subject matter authority to present topics to management and during inspections.</p></li><li><p>Monitors quality system metrics including deviations, corrective actions, change management and controlled document workflows.</p></li><li><p>Drafts and implements long-term planning for the process, staff and budget.</p></li><li><p>Performs personnel management functions (i.e. annual employee evaluations, coaching, mentoring, performance feedback, etc.).</p></li><li><p>Makes decisions and develops and implements policies.</p></li><li><p>Ensures that policies and procedures are effectively coordinated and follow regulatory requirements and current good manufacturing practices (cGMPs).</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Have previous quality experience in the pharmaceutical industry</p></li><li><p>You continuously seek to improve processes for improved performance</p></li><li><p>Enjoy leading a team of Quality minded professionals</p></li></ul><p>To be considered for this role you must hold a BA / BS degree in Life Sciences or related field and 6+ years of relevant cGMP manufacturing experience. Also, must have 3 years of supervisory experience. May substitute proven experience for education requirement.</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>$90,800.00 - $148,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Feb 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Dir Health Economics & Outcomes Research, Solid Tumors]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45357]]></requisitionid>
    <referencenumber><![CDATA[R45357]]></referencenumber>
    <apijobid><![CDATA[r45357]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45357/assoc-dir-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>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.</p><p><br>This position is at our Sleepy Hollow, NY location and will require you to be onsite 4 days/week. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong><br>• Develop and implement global HEOR strategies and programs for our portfolio 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 future 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 future 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 learnings to pipeline products.<br>• Maintain an up-to-date awareness of regulatory (e.g. FDA, EMA) 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 may be for you if you:</strong><br>• Want to have an impact on patient lives<br>• Enjoy working in a ‘rapid response’ environment<br>• Would like an opportunity to present to senior leaders<br>• Want to be part of a growing high performing team</p><p>To be considered it is required to have an Advanced graduate degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field (e.g. pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health). 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. Strong technical expertise required in design and conduct of HEOR studies and models. Solid understanding of regulatory (e.g. FDA, EMA) and HTA considerations. Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data. Experience with Oncology is preferred. <br> </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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager,  QA (Sustaining Engineering)]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42269]]></requisitionid>
    <referencenumber><![CDATA[R42269]]></referencenumber>
    <apijobid><![CDATA[r42269]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r42269/associate-manager-qa-sustaining-engineering/]]></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>We are currently looking to fill a Manager, Medical Device Quality Assurance position on our Medical Device Sustaining Engineering QA team. This position will provide QA oversight of the Medical Device function including combination products, including pre-filled syringe and auto-injectors/pen injectors for biological therapeutics developed internally and in collaboration with partners and CMO’s. Supports the work using quality risk management principles and their application to medical device development and commercialization. The scope will involve collaboration with internal and external partners, primarily post-transfer and commercial activities.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Provide leadership to team, including sustaining engineering support.</p></li><li><p>Support sustaining engineering programs through risk evaluation, design change, and maintain the design history file</p></li><li><p>Advise and participate in Design Reviews associated with combination products and/ or medical devices</p></li><li><p>Maintain the quality risk management file for commercial combination products within Regeneron including data driven risk assessments (risk identification, analysis and ranking)</p></li><li><p>Provide QA oversight and support to combination products in the sustainability phase of commercialization</p></li><li><p>Provide technical support to quality engineers and regulatory team during maintenance of the combination product</p></li><li><p>Responsible for the management and development of quality engineering team members</p></li><li><p>Represent Regeneron’s medical device QMS during regulatory inspections and partner audits</p></li><li><p>Interact with partners and contract organizations to ensure accurate completion of project achievements, including impact of changes and post-commercialization activities</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Thrive in a quality focused environment</p></li><li><p>Have proven experience in global applications of Quality Assurance and Quality Risk Management in the medical device/combination products field</p></li><li><p>Possess excellent written, oral, and interpersonal communication skills with ability to effectively interact with a broad spectrum of audiences</p></li></ul><p>To be considered for this role you must hold a Bachelors degree in Mechanical or Biomedical engineering or equivalent with the following amount of related experience in the pharmaceutical/medical device/biotechnology industry:</p><ul><li><p>Associate Manager – 6+ years</p></li><li><p>Manager – 7+ years</p></li></ul><p>Level is determined based on qualifications relevant to the role.</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>$90,800.00 - $173,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Corporate Accounting]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45377]]></requisitionid>
    <referencenumber><![CDATA[R45377]]></referencenumber>
    <apijobid><![CDATA[r45377]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45377/associate-manager-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>The Associate Manager, Corporate Accounting is a key contributor within the accounting organization, responsible for overseeing core accounting activities. This role partners closely with Finance, Financial Reporting, IT, Facilities, and other business stakeholders to deliver accurate financial information, ensure compliance with accounting policies, and maintain effective internal controls. In addition, the Associate Manager plays an integral role in driving process improvements, enhancing operational efficiency, and helping scale accounting operations to support a growing organization.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><p>• Managing the timely and accurate completion of the monthly accounting cycle for areas of responsibility<br>• Reviewing and preparing journal entries, supporting schedules, account analyses, reconciliations and variance explanations<br>• Ensuring proper accounting and compliance with the Company’s accounting policies for capital expenditures, leases, prepaid expenses, and other areas of responsibility<br>• Presenting monthly financial results to Senior Management including the Corporate Controller and the CFO<br>• Ensuring accuracy of 10Q/K financial statement notes related to areas of responsibility <br>• Ensuring that (i) effective internal controls are in place and are adhered to and (ii) associated internal control documentation is prepared and/or updated on a timely basis<br>• Facilitating quarterly and annual requests from internal and external auditors and leading SOX walkthroughs<br>• Reviewing and updating the relevant Company accounting policies to reflect changes in the business or accounting guidance<br>• Assisting in supporting Oracle Fusion Cloud Financials ERP implementation project<br>o Performing user acceptance testing, and ensuring workpapers and process documentation is updated as appropriate<br>• Managing and participating in continuous improvement initiatives and special projects as necessary</p><p><br><strong>The Role Might be for You If You:</strong></p><ul><li>Possess in-depth accounting knowledge gained through a mix of public accounting and hands-on corporate accounting experience</li><li>Can effectively communicate across all levels of the organization and build rapport with stakeholders</li><li>Are coachable and dependable with a willingness to learn and determination to drive tasks to completion</li><li>Have experience leading, coaching and developing team members</li></ul><p>To be considered for this role, you must have 5+ years of accounting experience and 1+ year(s) in a people management role. Strong analytical skills and attention to detail are critical. Must be able to operate in a fast-paced environment and handle multiple priorities.</p><p>Big 4 Accounting experience and CPA or CPA track are preferred. High proficiency with Microsoft applications is required, specifically Microsoft Excel. Experience with Oracle GL, Smartview, and Oracle Fixed Asset Module a plus. ERP implementation experience a plus.</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>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 08:56:53 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology - South Florida]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45442]]></requisitionid>
    <referencenumber><![CDATA[R45442]]></referencenumber>
    <apijobid><![CDATA[r45442]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45442/medical-specialist-ii-ophthalmology-south-florida/]]></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[<p><strong>Territory: South Florida</strong> (Miami, West Palm Beach, Ft Lauderdale, Naples, Ft Myers, Sarasota, and other surrounding cities)</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.</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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Allergy/ENT-Minneapolis North]]></title>
    <date><![CDATA[Thu, 26 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44453]]></requisitionid>
    <referencenumber><![CDATA[R44453]]></referencenumber>
    <apijobid><![CDATA[r44453]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44453/medical-specialist-i-allergyent-minneapolis-north/]]></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>Geography: Minneapolis, North Allergy/ENT territory</strong></p><p><strong>Key Markets include Minneapolis, MN, Duluth, MN, Fargo, ND, and Bismark, ND</strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with <strong>a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Feb 2026 15:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, Cell Culture Development]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45686]]></requisitionid>
    <referencenumber><![CDATA[R45686]]></referencenumber>
    <apijobid><![CDATA[r45686]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45686/process-development-engineer-ii-cell-culture-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>Regeneron’s Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated Process Development Engineer II to work as part of the late-stage development team to develop production processes of monoclonal antibodies in a non-GMP process development laboratory. In this role, they will perform studies at bench scale to conduct cell line selection, perform medium and feed development, and define optimal and robust upstream processes in support of clinical or commercial manufacturing production.</p><p><strong>A Typical Day in the Role of Process Development Engineer II Might Look Like:</strong></p><ul><li>Conducting statistical data analysis and leveraging Quality by Design (QbD) framework to define commercial processes for biologics</li><li>Coaching and mentoring developers in a matrixed environment</li><li>Designing and executing cell culture studies in single-use bioreactors (including AMBR250 system), and glass bench scale bioreactors (2L to 15L scale)</li><li>Operating and maintaining bioreactor and analytical equipment, preparing media and feed, generating cell banks</li><li>Generating, analyzing, and managing critical data in a highly organized manner</li><li>Coordinating and collaborating with colleagues from other groups involved in the research process, including cell line development, bioreactor scale-up, purification, analytics, and manufacturing.</li><li>Authoring technical documents, entering electronic lab notebook entries, and reviewing manufacturing records</li><li>Active involvement in technology transfer via written process transmittals, and by providing troubleshooting, process understanding, and on-site support to manufacturing production campaigns in Albany, NY</li><li>The position requires work on weekends and occasional travel to upstate NY</li></ul><p><strong>This Job May Be For You If:</strong></p><ul><li>You have exceptional written and oral communication skills, with the ability to effectively engage and collaborate with stakeholders at all levels within a matrixed organization, including technical teams, management, and external vendors.</li><li>You possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, direct projects, and mentor developers.</li><li>You have strong initiative to complete ambitious projects and drive new technology implementation.</li><li>You have experience in development of cell culture processes, experimental design, statistical analysis of data, and process characterization experience for commercial-enabling processes.</li><li>You have proven experience working independently and within a team environment on multiple projects simultaneously in an R&D laboratory setting.</li></ul><p>This role requires a Master’s degree in Chemical Engineering or Bio-related Engineering with 3-6 years, or a Bachelor’s degree (6+ years) of experience in a laboratory setting.</p><p><strong>Preferred:</strong></p><ul><li>Experience with mammalian cell culture; developing fed-batch bioreactor commercial processes including leveraging Quality by Design (QbD) framework; statistical design and analysis software (i.e., JMP).</li><li>Experience with technology transfer to manufacturing facilities and providing person-in-plant support and troubleshooting for upstream commercial processes.</li><li>Demonstrated leadership abilities, prior mentorship experience, and a track record of successfully managing cross-functional projects and/or teams.</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>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Software Engineer (Genomics)]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44731]]></requisitionid>
    <referencenumber><![CDATA[R44731]]></referencenumber>
    <apijobid><![CDATA[r44731]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44731/principal-software-engineer-genomics/]]></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>SUMMARY:</strong></p><p>We are seeking a Principal Software Engineer (Genomics), who can help develop and maintain computational software, tools, and applications to analyze and interpret millions of sequenced and deeply phenotyped human samples. To enable Regeneron to deliver better medicines to patients, we must empower our scientists to efficiently generate and interact with association analysis results from massive human genetics experiments. You will deliver high-quality, production-level, and flexible tools that help scientists perform large scale genomic analysis and explore and interpret their results. A proven track record of implementing software and pipelines in a cloud-based computing environment (such as Amazon Web Services or Google Cloud Platform) is essential for this role.</p><p><strong>As Principal Software Engineer (Genomics), a typical day may include:</strong></p><p>· Design and implement software applications to fit users’ needs based on shifting state-of-the-art genetic analysis methods, opportunities and priorities.</p><p>· Modernize and optimize existing code bases to improve performance and create scalable, portable, unit tested code.</p><p>· Designing and maintaining robust, cloud-based genomic analysis platforms capable of processing petabytes of genomic data.</p><p>· Implementing comprehensive data management solutions that ensure FAIR data principles.</p><p>· Interact with other developers on the team and jointly develop code to address high-priority tasks.</p><p>· Provide user support by answering questions, understanding specific use cases, fixing bugs, and writing documentation.</p><p>This role could be for you if you:</p><p>· Have a strong foundation in the current best practices of software engineering.</p><p>· Enjoy developing tools and solving challenging problems to aid scientists in performing creative analysis.</p><p>· Have a proven record of implementing scalable software tools, applications and workflows and in a cloud-based computing environment.</p><p>· Enjoy directly interacting with users to identify and develop solutions for their needs.</p><p>· Skilled in software development and is familiar or has a strong interest in human genetics or computational genomics.</p><p>· Can effectively communicate methods and present code to a variety of technical audiences.</p><p>· Enjoy working in a highly interactive environment with a diverse team of colleagues.</p><p><strong>To be considered for this role, you must have:</strong></p><p>· At least a Masters degree in Computer Science, Bioinformatics, Biomedical Engineering, or related field with at least 6 years of relevant experience in Computational Biology or a related field. A Doctoral degree in Computer Science, Bioinformatics, Biomedical Engineering, or related field is also encouraged.</p><p>· Extensive experience with cloud computing platforms (AWS, GCP, or Azure) and containerization technologies.</p><p>· Strong background in developing and optimizing high-performance computing solutions for large-scale genomic data analysis.</p><p>· Proven experience with version control systems, CI/CD pipelines, and other modern software development practices.</p><p>· Deep expertise in multiple programming languages (e.g., Python, C++) and experience with genomic analysis tools.</p><p>· Experience building and maintaining databases and API layers is preferred.</p><p>​#RGC</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-West Virginia]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45788]]></requisitionid>
    <referencenumber><![CDATA[R45788]]></referencenumber>
    <apijobid><![CDATA[r45788]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45788/medical-specialist-i-pulmonology-west-virginia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Charleston]]></city>
    <state><![CDATA[West Virginia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: West Virginia - representative must reside within or close to the territory.</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>As a Medical Specialist, a typical day might include the following:</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 may be for you if you:</strong></p><ul><li><p>Are confident in demonstrating strong and consistent sales performance that exceeds expectations related to goals</p></li><li><p>Are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>Can demonstrate a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>Collaborate effectively with internal and external partners</p></li><li><p>Share a passion and learning interest in science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li></ul><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. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. 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. Ability to travel and cover large geographic territories.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 09:56:45 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45600]]></requisitionid>
    <referencenumber><![CDATA[R45600]]></referencenumber>
    <apijobid><![CDATA[r45600]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45600/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[<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><p><strong>As an Associate Biotech Production Specialist, a typical shift might include, but is not limited to, the following:</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><br><strong>This role might be for you if:</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><br>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><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><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 / Car Valet</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>#LI-Onsite #JOBSIEST #REGNIELSM #IRELIM</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Biostatistics - Safety Statistics]]></title>
    <date><![CDATA[Fri, 06 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45852]]></requisitionid>
    <referencenumber><![CDATA[R45852]]></referencenumber>
    <apijobid><![CDATA[r45852]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45852/senior-director-biostatistics-safety-statistics/]]></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>Regeneron Pharmaceuticals is seeking a Senior Director, Biostatistics - Safety Statistics to join our organization!!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Senior Director, Biostatistics, will lead a new capability group within the Biostatistics department, focused on working closely with Global Patient Safety (GPS) Sciences and will partner with GPS to bring the best statistical approaches for GPS’ core mission of safety surveillance, signal detection, communication of the safety profile, and benefit risk assessment, as well as giving statistical input to regulatory agency submissions and queries. The incumbent will establish the vision and direction for this new group. The Biostatistics Safety Group (BSG) will collaborate closely with the therapeutically aligned statisticians within Biostatistics, as well as the Clinical Development Units, Regulatory Affairs, Statistical Programming, Data Management, and Medical Writing. The BSG works on products in the Regeneron portfolio ranging from pre-IND through approval and post-marketing, with a focus on evaluation, interpretation, and reporting of aggregate/integrated safety data, including benefit risk planning and assessment. The group will also be responsible for ensuring the integrity of safety monitoring in open-label studies and for managing the interface with IDMCs. </p><p>Regeneron is seeking an experienced statistician to lead this new group. The leader will build the strategy, operating model, processes, and team to partner closely with GPS and to ensure robust, compliant, and innovative evaluation of aggregate safety data. The Senior Director, Biostatistics Safety Group, will report to VP Biostatistics and work with colleagues in Biostatistics, BDM, GPS, Regulatory and with CDU leadership to establish a vision and resourcing model for the group.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Oversee development of key processes and templates for analyzing safety data from Regeneron clinical development projects, including safety-related contents of Statistical Analysis Plans (SAPs) and Integrated Summary of Safety Statistical Analysis Plans (ISS SAPs) ensuring consistency, quality, and audit-readiness across programs.</p></li><li><p>Provide strategic input to and oversight of the development of Safety SAPs and ISS SAPs</p></li><li><p>Assess the impact of safety findings of external data on Regeneron-developed medications, and assess the impact of new regulatory guidances on how Regeneron analyzes and interprets safety data. </p></li><li><p>Provide strategic input on safety related submissions to regulatory agencies and responses to requests from regulatory agencies.</p></li><li><p>Provide strategic statistical leadership for safety deliverables across the portfolio (pre-IND to post-marketing), including integrated safety analyses to support regulatory submissions and responses.</p></li><li><p>Serve as statistical lead at regulatory meetings; guide statistical strategy for safety-related briefing materials, queries, and inspection readiness.</p></li><li><p>Lead statistical contributions and provide oversight of contributions by Safety Statistics to benefit-risk planning and assessment, including ensuring effective delivery and communication of benefit-risk data analyses and visualizations to internal and external stakeholders.</p></li><li><p>Ensure appropriate interpretation of safety deliverables in collaboration with other functions.</p></li><li><p>Oversight of the development, and timely delivery and interpretation of high-quality safety outputs, including graphics.</p></li><li><p>Oversight of cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.</p></li><li><p>Oversight to ensure the delivery of high-quality outputs according to agreed-upon timelines.</p></li><li><p>Identify potential areas to improve processes or statistical methodologies, initiate steps to evaluate possible improvements and develop a plan to implement changes based on this evaluation.</p></li><li><p>Lead and/or represent Biostatistics on cross-functional efforts to implement strategic initiatives that address processes related to monitoring, assessing, interpreting, and reporting safety data.</p></li><li><p>Represent Regeneron on external initiatives to advance the safety discipline (e.g., ASA, PHUSE, DIA, etc.), in collaboration with Statistical Programming and Biostatistics.</p></li><li><p>Mentor team members and provide appropriate development opportunities.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>MS (with at least 15+ years of experience) or PhD (with at least 10+ years of experience) in Statistics, Biostatistics, or a highly related field, with at least 9 years (MS) or 7 years (PhD) of experience in pharmaceutical development.</p></li><li><p>Minimum of 2 years of management experience required for people managers.</p></li><li><p>Excellent English communication skills, both oral and written</p></li><li><p>Advanced knowledge of statistical methodology including experimental design, descriptive statistics, inferential statistics, and statistical programming.</p></li><li><p>Must have demonstrated exemplary statistical experience in managing and completing multiple projects or equivalent experience.</p></li><li><p>In-depth knowledge and understanding in application of standard business procedures (regulatory guidance, global regulations, ethical issues associated with scientific research trials, SOPs, etc.).</p></li><li><p>Experience interacting with regulatory agencies.</p></li><li><p>Experience in leading NDA, BLA, and or CTD submission preferred.</p></li><li><p>Oversight of multiple safety-related projects (e.g., ISS, SSAP, benefit-risk assessment, signal detection).</p></li></ul><p>#GDBDMJobs</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>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Mar 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, SDLC, Testing & Release Management]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44112]]></requisitionid>
    <referencenumber><![CDATA[R44112]]></referencenumber>
    <apijobid><![CDATA[r44112]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44112/director-sdlc-testing-release-management/]]></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>The Director of SDLC, Testing & Release Management will own, develop, and execute the strategic vision for SDLC, CI/CD, testing, release management, and AI‑augmented automation across the enterprise to accelerate digital transformation that includes deployment and upgrades of several GMP IT solutions.</p><p>As a Director, a typical day might include the following:</p><ul><li>Establish and govern standardized SDLC processes ensuring consistency, efficiency, speed and compliance.</li><li>Build, train and guide internal IT SDLC team on SDLC and CSA processes and requirements, development of effective and efficient test plans, compliant documentation ready for QA approval. Serve as the organizational authority for Computer Software Assurance (CSA).</li><li>Develop test automation frameworks including LLM‑ and AI‑driven testing. Enhance release management processes for reliability and continuity.</li><li>Lead and mentor a cross‑functional organization, partner with QA, Compliance, and Regulatory teams to accelerate new system implementations and system changes.</li><li>Define and improve quality metrics and KPIs including AI‑enabled indicators.</li><li>Drive adoption of modern testing methodologies and AI‑assisted validation, establish robust test data management practices. Oversee risk evaluation of emerging technologies including LLMs.</li><li>Ensure compliance with CSA, CSV, Part 11, Annex 11, GAMP 5. Enforce documentation standards, including automated draft content generation.</li><li>Serve as the primary escalation point. Represent test and release functions at executive forums.</li></ul><p>This role may be for you if you have:</p><ul><li>CI/CD: Jenkins, GitLab CI, GitHub Actions.</li><li>Testing: Selenium, JUnit, TestNG, Cypress, Playwright.</li><li>AI/LLM: testing tools, prompt engineering, model governance.</li><li>IaC: Terraform, Ansible.</li><li>Cloud & Containers: Docker, Kubernetes.</li><li>Monitoring: Prometheus, Grafana, ELK.</li><li>Version Control: Git, SVN.</li><li>Work Management: Jira, Confluence, Azure DevOps.</li><li>Validation Systems: electronic validation platforms.</li><li>Change‑management leadership with strong decision‑making, risk‑management skills and budget/resource planning.</li><li>Compliance leadership including AI‑enabled systems.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Associate Director: 10 + years industry experience in Information Systems and Technology with 8+ years of managing employees and budgets, 7+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment plus experience with IT Compliance guidelines as per GAMP 5.</li><li>Director: 12+ years working in Information Systems and Technology with 10+ years of managing employees and budgets, 10+ years working in a GMP manufacturing environment and experience in a biotech/pharma environment plus experience with IT Compliance guidelines as per GAMP 5.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</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>$147,800.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sample Management Associate]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45879]]></requisitionid>
    <referencenumber><![CDATA[R45879]]></referencenumber>
    <apijobid><![CDATA[r45879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45879/sample-management-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>A Sample Management Associate supports biobanking operations efficiently and effectively while beginning to independently lead sample data processes. Possesses a thorough knowledge and understanding of clinical/non-clinical study protocols and associated documentation. Is fully capable of multi-tasking across assignments. Works with clients directly in a team environment. The incumbent may help in assessing and investigating new opportunities that will lead to increased efficiencies and improved productivity with regards to biobanking operations.</p><p><strong>As a Sample Management Associate, a typical day may include:</strong></p><ul><li><p>Trains on clinical/non-clinical study protocols and associated study documentation to build knowledge of study conduct as it pertains to biospecimen management. Executes study reference file creation by interpreting protocols and other applicable data inputs with guidance.</p></li><li><p>Performs the accessioning and receipt of non-clinical/clinical samples by assessing and verifying data, both manually and with automated platforms such as Microsoft VBA and Streamlit. May identify and communicate issues with automated platforms to drive resolution.</p></li><li><p>Has an in-depth knowledge of Microsoft Excel and can analyze discrepancies in sample metadata using complex formulas with limited guidance.</p></li><li><p>Drives necessary operations in applicable software systems (e.g., LIMS, ELN, etc.) to perform specimen and data management. Has the ability to identify and troubleshoot routine challenges.</p></li><li><p>Fulfills clinical/non-clinical sample requests to support bioanalysis deliverables as well as company-wide research initiatives.</p></li><li><p>Facilitates the completion and review sample transfer documentation, as applicable.</p></li><li><p>Responsible for assigning and coordinating sample management activities for assigned programs under limited guidance.</p></li><li><p>Under supervision, executes the reconciliation and data cleaning of biospecimens to drive deliverables forward.</p></li><li><p>May be responsible for the review of study documents to support study start up and protocol amendments.</p></li><li><p>Ensures a state of audit readiness. Assists in the preparation of supporting documents for Quality Audits, as applicable. May participate in study audit activities.</p></li><li><p>Provides cross-functional support to other sample management teams, as needed.</p></li><li><p>May assist with the training of other laboratory staff.</p></li><li><p>Participates in sub-group meetings and may shares results or progress of work with others.</p></li><li><p>Responsible for his/her own safety in the laboratory, as well as for the safety of co-workers and visitors.</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Ensure compliance and proper documentation in accordance with SOPs, and applicable regulations.</p></li><li><p>Handle high priority and multiple tasks within the appropriate timeframe while maintaining accuracy. Adapts to changing priorities. Is capable of multi-tasking across assignments.</p></li><li><p>Capable of identifying and troubleshooting problems pertaining to clinical/non-clinical protocols and associated documents as well as routine sample management processes and/or procedures.</p></li><li><p>Collaborates and maintains effective verbal and written communication with internal and/or external stakeholders to facilitate data discrepancy resolution. Communicates with CRO’s and third-party vendors to support biospecimen operations.</p></li><li><p>Communicates optimally with their manager and actively seeks out feedback to deepen self-development.</p></li></ul><h3>To be considered for this role, you must meet the following:</h3><ul><li><p>Bachelor’s degree</p></li><li><p>Typically, 2-4 years of relevant post-degree laboratory experience for Bachelor’s degree</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>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Global Procurement- CRO]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44608]]></requisitionid>
    <referencenumber><![CDATA[R44608]]></referencenumber>
    <apijobid><![CDATA[r44608]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44608/associate-director-global-procurement-cro/]]></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 currently looking to fill an Associate Director Global Procurement, R&D position within our team. In this role you will be responsible for all Procurement activities in support of the global clinical CRO category. As an Associate Director will manage categories with high degree of complexity, as well as executing challenging supplier negotiations and delivering high service level to the business. In this role, you must demonstrate the capability to proactively manage a supply base and maximize value, minimize risk, and ensure quality & cost effectiveness by working collaboratively with business unit.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Help define and implement the global CRO Category strategy to serve global and regional business needs.</p></li><li><p>Work closely with stakeholders to lead discussions related to the CRO Category and aligns category priorities with Procurement management and stakeholders.</p></li><li><p>Manage negotiations, supplier management activities, and stakeholder engagement activities for the CRO Category as assigned.</p></li><li><p>Work with leadership to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Manage category activities to ensure compliance with appropriate GxPs and other applicable regulations, as applicable.</p></li><li><p>Demonstrate knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li><li><p>Can directly or through a matrix structure, manage team of professional level employees responsible for performing category management tasks (if applicable.)</p></li><li><p>Can provide coaching and guidance on job performance and career development to direct reports (if applicable) and provides leadership examples for the organization.</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Can negotiate contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li><li><p>Have working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Have the ability to leverage standard business applications for communicating, presenting and analyzing (Word, Excel, PowerPoint)</p></li><li><p>Have used external data sources, market information, and supplier engagement to constantly improve Regeneron’s knowledge of supply market dynamics.</p></li><li><p>Are able to demonstrate success managing cross-functional teams to drive results in Clinical Trial categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Can demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including experience in Pharma/BioPharma.</p><ul><li><p>Associate Director level: 10+ years of experience in relevant experience, functions or industries. The ideal candidate will have in-depth knowledge of managing global category processes, and suppliers across a breadth of categories</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Commercial Operations, UK and Ireland]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44039]]></requisitionid>
    <referencenumber><![CDATA[R44039]]></referencenumber>
    <apijobid><![CDATA[r44039]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44039/associate-director-commercial-operations-uk-and-ireland/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Commercial Operations Lead to join our team in Uxbridge, supporting our commercial business across the UK and Ireland<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.</p><p>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><h3><strong>A Typical Day:</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 May Be For You:</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 value accuracy and clarity in communications, especially when supporting external teams.</p></li><li><p>You take pride in mentoring others and encouraging team growth.</p></li><li><p>You’re motivated by solving operational challenges that support patient-impacting work.</p></li></ul><p><strong>To be considered</strong></p><p>You’ll need to bring significant leadership experience in Commercial Operations within the UK & Irish biopharmaceutical industry. A strong grasp of market dynamics, local laws, and reporting requirements is important. You should be confident navigating analytics, experienced with tools like PowerPoint, Excel, Veeva, and WORD, and able to communicate fluently in English. Prior experience supporting field sales in a pharma setting is desirable, along with a Bachelor’s degree and at least 7 years of industry experience, including 5 years in global commercial operations.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 09:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Submission Project Management (RSPM)]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44752]]></requisitionid>
    <referencenumber><![CDATA[R44752]]></referencenumber>
    <apijobid><![CDATA[r44752]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44752/manager-regulatory-submission-project-management-rspm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced and detail-oriented Manager, Regulatory Submission Project Management (RSPM) to join our dynamic team. This pivotal role offers the opportunity to lead the planning, execution, and review of regulatory operations activities, ensuring the successful submission of regulatory documents and data to health authorities. If you thrive in a collaborative environment and are passionate about driving regulatory milestones, this position could be your next career step.</p><p><strong>A Typical Day:</strong><br>As a Manager, Regulatory Submission Project Management, your day may include:</p><ul><li>Collaborating with cross-functional teams to create submission timelines and responsibility matrices.</li><li>Guiding teams and resolving issues related to submission documents to maintain quality and timeliness.</li><li>Managing submission deliverables and coordinating with Regulatory Publishing and vendors on document status.</li><li>Reviewing submission content plans and validating documents for compliance with health authority guidelines.</li><li>Supporting PMDA consultations, Clinical Trial Notifications, PCAs, MCNs, and NDAs through operational excellence.</li><li>Maintaining submission templates and obtaining literature references to support submissions.</li><li>Ensuring consistency and standardization across regulatory submissions.</li><li>Tracking and managing metadata within the electronic data management system (EDMS).</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You have a strong knowledge of Regulatory Agency regulations, guidelines, and specifications (e.g., PMDA, FDA, EMA, and ICH).</li><li>You excel in project management and timeline management for regulatory submissions.</li><li>You enjoy working with submission processes and systems such as Veeva Vault RIM or docuBridge.</li><li>You are adept at eCTD preparation and validation processes.</li><li>You thrive in fast-paced environments and can adapt quickly to changing priorities.</li><li>You have strong proficiency with MS Office applications and Adobe Acrobat.</li><li>You value collaboration and have exceptional attention to detail.</li><li>You are driven by the opportunity to make meaningful contributions to regulatory milestones.</li></ul><p><strong>To Be Considered:</strong><br>To excel in this role, you must have a Bachelor's Degree and at least six years of pharmaceutical industry or relevant experience. Strong knowledge of submission processes, eCTD guidelines, and regulatory tools is essential. Proficiency with systems like Veeva Vault RIM and docuBridge is highly desirable. Native level fluency in Japanese and business level English is required.</p><p>This is your chance to be part of a team that drives impactful regulatory submissions while fostering innovation and collaboration. Apply now to make a difference in regulatory excellence!</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Site Management and Monitoring]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44535]]></requisitionid>
    <referencenumber><![CDATA[R44535]]></referencenumber>
    <apijobid><![CDATA[r44535]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44535/senior-manager-global-site-management-and-monitoring/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. We’re looking for a Senior Manager, Global Site Management and monitoring, to join our team and play a pivotal role in coordinating and improving the delivery of clinical trial operations. In this role, you’ll contribute to the planning, execution, and oversight of our clinical trial portfolio, ensuring collaboration among internal teams, external vendors, and investigator sites. With opportunities to drive innovation and process improvement, this position offers meaningful impact in advancing clinical trial strategies and methodologies.</p><h3><strong>A Typical Day:</strong></h3><ul><li><p>Develop and be responsible for study-specific risk-based monitoring strategies to ensure compliance and efficiency, while managing vendor relationships, including onboarding, performance evaluations and resource alignment.</p></li><li><p>Collaborate with Clinical Trial Management teams to design monitoring strategies aligned with RBQM methodologies, including budget planning and approval.</p></li><li><p>Provide input to monitoring plans, ensuring alignment with critical data specifications and SDR/SDV approaches.</p></li><li><p>Oversee and evaluate performance metrics and risk indicators, providing intervention as needed.</p></li><li><p>Act as an SME for monitoring/site management topics, offering guidance to internal and external stakeholders.</p></li><li><p>Support inspection readiness activities and participate in regulatory GCP inspections and audits.</p></li></ul><h3><strong>This Role May Be For You If:</strong></h3><ul><li><p>You have extensive experience with risk-based quality operating models and clinical trial operations.</p></li><li><p>You excel in collaborative environments while maintaining the ability to work independently.</p></li><li><p>You are skilled in establishing relationships with stakeholders and translating strategies into actionable frameworks.</p></li><li><p>You are familiar with medical terminology and industry regulations, including ICH/GCP standards.</p></li></ul><h3><strong>To Be Considered:</strong></h3><p>Applicants must have a Bachelor’s Degree and at least 8 years of proven experience in clinical trial operations, monitoring, and site management. A proven understanding of ICH/GCP standards and familiarity with medical terminology are crucial. Preferred qualifications include experience in risk-based monitoring methodologies and expertise in collaborating with CROs and FSPs. This position involves travelling up to 10% of the time to support site management activities.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Pulmonology/Cardiology]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46016]]></requisitionid>
    <referencenumber><![CDATA[R46016]]></referencenumber>
    <apijobid><![CDATA[r46016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46016/medical-director-clinical-development-pulmonologycardiology/]]></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 Medical Director, Clinical Development, Specialty Medicine should be a qualified physician with pharmaceutical industry experience, preferably in the area of Pulmonary/Critical Care Medicine or Cardiology, in relevant areas such as pulmonary hypertension. The Director will serve as Medical Lead for clinical trials in the CDP and is responsible for the design of clinical study concepts leading to clinical trial protocols. 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><strong>A typical day in the life of a Medical Director may include the following responsibilities:</strong></p><ul><li>Acts as medical expert and leader in interactions with external stakeholders</li><li>Defines clinical trial-related Clinical Development Program (CDP) goals and objectives </li><li>Works closely with discovery teams to provide input on the next generation of targets in the field</li><li>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts </li><li>Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings</li><li>Leads the Global Clinical Study Team to produce high quality program deliverables on schedule </li><li>Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety </li></ul><p><strong>This job may be for you if you have the following:</strong></p><ul><li>An M.D. or equivalent with board eligibility or board certification in Pulmonary/Critical Care or Cardiology preferred; relevant experience can be acceptable.</li><li>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</li><li>Experience in cardiovascular disease drug development strongly preferred</li><li>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</li></ul><p>#MDJobsCD, #MDJobs, #GDTherapeuticJobs</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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Obesity]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44958]]></requisitionid>
    <referencenumber><![CDATA[R44958]]></referencenumber>
    <apijobid><![CDATA[r44958]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44958/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[<div>The Medical Director, Clinical Development, Obesity should be a qualified physician with pharmaceutical industry experience, preferably in the area of metabolism, in relevant areas such as obesity or Type 2 diabetes. The Director will serve as Medical Lead for clinical trials in the CDP and is responsible for the design of clinical study concepts leading to clinical trial protocols. 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.</div><div><div><div><div><div><div><div><div><div><div><div><div><p><strong>A typical day in the life of a Medical Director may include the following responsibilities:</strong></p><ul><li>Acts as medical expert and leader in interactions with external stakeholders</li><li>Defines clinical trial-related Clinical Development Program (CDP) goals and objectives </li><li>Works closely with discovery teams to provide input on the next generation of targets in the field</li><li>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts </li><li>Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings</li><li>Leads the Global Clinical Study Team to produce high quality program deliverables on schedule </li><li>Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety </li></ul><p><strong>This job may be for you if you have the following: </strong></p><ul><li>An M.D. or equivalent with board eligibility or board certification in Endocrinology preferred; relevant experience can be acceptable.</li><li>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</li><li>Experience in metabolic disorders drug development strongly preferred</li><li>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</li></ul><p>#MDJOBS, #MDJOBSCD#GDTherapeuticJobs</p></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>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Mar 2026 16:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I, Bioconjugation Development]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45791]]></requisitionid>
    <referencenumber><![CDATA[R45791]]></referencenumber>
    <apijobid><![CDATA[r45791]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45791/process-development-engineer-i-bioconjugation-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>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking and dynamic Process Development Engineer I for its new Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will develop conjugation and purification processes for bioconjugation of proteins to a diverse range of smaller-molecules. You would work in close collaboration with cross-functional teams for process development and optimization using the principles of Quality by Design (QbD) to make the processes suitable for GMP production. This role also involves process scale-up and technology transfer of manufacturing related workflows to Contract Development and Manufacturing Organizations (CDMOs) or Regeneron based manufacturing suites to ensure timely and reliable entrance to the clinic through product commercialization.</p><h3><strong>A typical day in the role of Process Development Engineer I might include:</strong></h3><ul><li><p>Working at the bench to design and develop scalable, robust and controlled GMP-ready bioconjugation and purification processes.</p></li><li><p>Collaborating with analytical groups within or outside the organization to establish supportive analytical characterization techniques.</p></li><li><p>Discussing plans and data in cross functional teams to evaluate processes and determine developmental goals and ensure integrated program success.</p></li><li><p>Proactively complying to lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</p></li><li><p>Using statistical design of experiments (DOE) to optimize bioconjugation processes including conjugation reactions, purification operations, and analytical characterization.</p></li><li><p>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to provide technical assessment of CDMO’s intended for GMP production and successfully transferring processes with immediate, first-time success.</p></li><li><p>Researching, identifying, and developing new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT) to ensure robust and controllable bioconjugation and purification processes.</p></li><li><p>Authoring robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</p></li><li><p>Analyzing and presenting data in a clear and cohesive manner to a broad audience facilitating data-driven decision making.</p></li><li><p>Authoring, reviewing, or providing domain expertise for publications, reports, tech transfer documents, regulatory support documents and patents.</p></li><li><p>Being a responsible lab citizen by ensuring timely maintenance of lab equipment, keeping the lab tidy and organized and proactively planning for lab resources.</p></li><li><p>Coaching and mentorship of junior team members of the organization as needed.</p></li></ul><h3><strong>This role may be for you if you:</strong></h3><ul><li><p>Enjoy working in the lab to advance exciting new drug modalities to patients.</p></li><li><p>Have strong initiative and aim to complete challenging tasks and learn new technologies.</p></li><li><p>Have a strong fundamental understanding of various protein purification and technology transfer principles</p></li><li><p>Are capable of multi-tasking and working both independently and in a collaborative environment involving cross-functional teams.</p></li><li><p>Have excellent interpersonal, verbal and written communication skills.</p></li><li><p>Can think critically and demonstrate problem-solving skills.</p></li></ul><p>This role requires a Bachelor’s + 4 years relevant experience or Master’s+0-3 years relevant experience in chemical/biochemical engineering or a related field. Experience with antibodies in the bioconjugates space is highly preferable. Hands on experience with bioconjugation processes (lysine-based, cysteine-based, site-specific etc.) with practical knowledge of downstream purification techniques such as chromatography, ultrafiltration/diafiltration, membrane technologies etc. is preferred. Experience with a variety of analytical characterization tools such as electrophoresis, mass spectrometry, high-performance liquid chromatography (HPLC), UV spectroscopy, etc. is preferred.</p><p>Note: title will be commensurate with experience</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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Development Strategy Planning & Operations, Hematology]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44886]]></requisitionid>
    <referencenumber><![CDATA[R44886]]></referencenumber>
    <apijobid><![CDATA[r44886]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44886/associate-director-clinical-development-strategy-planning-operations-hematology/]]></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, Clinical Sciences Strategy and Planning, will partner with the Executive Director, Clinical Science Strategy and Excellence, to support the strategic and operational advancement of the assigned CDU(s) portfolio. This role will serve as a key operational partner, driving execution of critical initiatives while performing Chief of Staff functions for the department. The position requires close collaboration with the CDU leadership team, Clinical Scientist leadership, and cross-functional stakeholders to ensure alignment of priorities, effective communication, and operational excellence across Clinical Sciences.</p><p>This role is both strategic and tactical, requiring a nimble thinker with strong interpersonal skills, drug development and operational acumen, and the ability to pivot quickly as new data and priorities emerge. The ideal candidate will demonstrate the ability to translate strategic vision into operational execution while fostering cross-organizational collaboration.</p><p><strong>A typical day in the life of an Associate Director, Clinical Sciences Strategy and Planning may include the following responsibilities: </strong></p><ul><li>Partners with the Executive Director and CDU leadership team to drive and optimize critical Clinical Sciences initiatives, ensuring focus on the most impactful items for business success.</li><li>Supports the execution of key projects and initiatives within the portfolio, tracking progress and ensuring alignment with Regeneron's strategic goals and objectives.</li><li>Creates and maintains content for CDU communication platforms (e.g., intranet, SharePoint sites) to drive awareness and clarity about the Clinical Sciences strategy, organization, portfolio, and work activities.</li><li>Develops agendas for key internal meetings, facilitates effective discussions, documents clear action items, and drives communication and accountability within the Clinical Sciences organization.</li><li>Assists in driving pipeline planning activities for the CDU portfolio, working with the CDU Leadership Team and other key stakeholders to ensure continuity of corporate planning and execution.</li><li>Responsible for supporting cross-CDU resource and planning activities, including workforce/headcount planning, space planning, and quarterly/annual planning and budgeting processes.</li><li>Supports the Executive Director clinical trial excellence initiatives, implementation of next-generation technologies, and enterprise-wide initiatives by coordinating cross-functional workstreams and tracking deliverables.</li><li>Identifies and regularly reports on key performance metrics, providing insights and recommendations for enhancing team effectiveness and cross-organizational collaboration.</li><li>Supports the preparation of board meetings, executive team meetings, and other senior management meetings, including development of presentation materials and briefing documents.</li></ul><p>This role may be for you if you have the following:</p><ul><li>Advanced Degree in a scientific or business field preferred; MD, PhD, MBA, or PharmD strongly preferred.</li><li>Minimum of 7 years of relevant experience in clinical research, drug development, and/or pharmaceutical operations.</li><li>Proven ability to manage complex projects and drive operational excellence in a matrixed environment.</li><li>Excellent communication and interpersonal skills, with the ability to build strong relationships at all levels of the organization.</li><li>Strong analytical and problem-solving skills, with the ability to synthesize information and make informed recommendations.</li><li>Demonstrated experience in fostering cross-organizational collaboration and managing multiple priorities simultaneously.</li><li>Scientific acumen with the ability to understand and communicate complex clinical and scientific concepts.</li><li>Experience with strategic planning, portfolio management, or Chief of Staff functions preferred.</li><li>High level of integrity and professionalism, with the ability to handle sensitive information with discretion.</li><li>Proficiency in creating executive-level presentations and communications.</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 14:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations (Infrastructure Architecture)]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45562]]></requisitionid>
    <referencenumber><![CDATA[R45562]]></referencenumber>
    <apijobid><![CDATA[r45562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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[<p>The Associate Director of IT Operations (Infrastructure Architecture) ensures the reliable operation, delivery, and management of IT/Operational Technology (IT/OT) infrastructure and services, with a focus on supporting a highly regulated GxP environment. This role provides strategic direction, operational management, and administrative oversight for the daily IT operational activities, including hardware, communications & WiFi infrastructure, and service delivery. The position also ensures integration and alignment with corporate IT systems and infrastructure while maintaining robust compliance, security, and service standards.</p><p>As an Associate Director of IT Operations (Infrastructure Architecture), a typical day might include the following:</p><ul><li>Ensure the reliable operation of IT/OT infrastructure, including but not limited to servers, hardware, communications and desktop support, plus oversight of daily operational activities.</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.</li><li>Build scalable and secure wireless networks to support industrial and enterprise needs.</li><li>Provide operational management for data centre operations, network services, telecom, asset management, and security plus ensure systems and procedures are in place for effective monitoring and reporting.</li><li>Maintain compliance with industry standards, including experience with automation systems such as DeltaV/Emerson and Rockwell/Allen-Bradley.</li><li>Manage service providers to ensure high-quality service delivery and alignment to service level agreements (SLAs) and act as the escalation point for major incidents.</li><li>Ensure compliance with relevant regulations and standards, including GxP, FDA and other global regulatory requirements.</li><li>Maintain robust security measures to protect IT/OT infrastructure, including data integrity and disaster recovery planning.</li><li>Lead and mentor a diverse technical team and run recruitment, training, performance evaluations, and target setting for the IT Operations team.</li><li>Collaborate with partners to ensure seamless integration between IT and OT systems.</li><li>Provide regular management reporting on service performance and IT operations.</li></ul><p>​​​</p><p>This role may be for you if you:</p><ul><li>Have management and delivery experience including management of a diverse technical team, including Helpdesk, Desktop, Server and Network staff, with experience managing vendors and managed services.</li><li>Have experience in developing and deploying SLAs, Metrics and other best practices, as well as having successfully implemented ITIL practices into an organisation.</li><li>Have experience with Business Continuity and Disaster Recovery planning.</li><li>Have a strong background in Microsoft OS, in particular Server and GPO elements.</li><li>Have a strong understanding of Data Integrity and associated tools.</li><li>Possess hands-on experience designing and documenting infrastructure architecture across networking, compute, and security domains.</li><li>Have demonstrated experience with security frameworks (NIST CSF, IEC 62443, or ISO 27001) and applying them within regulated environments.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with</p><ul><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><li>Preferred knowledge of understanding of IT compliance guidelines, including PICS, CFR21 Part 11, Annex 11, and GAMP.</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>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist, Oncology (Histology and Immunohistochemistry)]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46021]]></requisitionid>
    <referencenumber><![CDATA[R46021]]></referencenumber>
    <apijobid><![CDATA[r46021]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46021/scientist-oncology-histology-and-immunohistochemistry/]]></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 Histology team is seeking a highly motivated Senior Associate Scientist/Scientist to join the Oncology/Immuno-Oncology department at Regeneron Pharmaceuticals, as we make transformational advances in harnessing the power of the immune system to fight cancer. The position will involve executing complex histological studies to reveal potential target expression and investigate the mechanism of action of novel immuno-oncology therapeutics. This role will be deeply involved in the development of cutting-edge therapeutics including bispecific antibodies, antibody-drug conjugates, and CAR-T cells. You will work closely with other team members and collaborators to advance programs spanning from initial target discovery to support of ongoing clinical-stage therapeutics.<br><br><strong>As a Senior Associate Scientist/Scientist, a typical day may include the following:</strong><br> </p><ul><li><p>Independent execution of immunohistochemistry (IHC) assays, including the use of high-throughput Ventana and Biocare autostainer platforms</p></li><li><p> RNA in-situ hybridization (ISH) based assays using modern platforms such as RNAscope.</p></li><li><p>Histological tissue processing, microtomy, cryosectioning, and H&E staining of human and non-human tissues</p></li><li><p>Development and characterization of novel antibodies and probes for IHC and ISH assays</p></li><li><p>Scanning of slides and assembly of images in PowerPoint and other formats for presentation</p></li><li><p>Basic analysis of images and frequent collaboration with members of the Pathology department</p></li></ul><p><strong>This role may be for you if:</strong><br> </p><ul><li><p>You have proven basic histology skills and a desire to further expand and develop your skill set and knowledge of the immuno-oncology drug development process.</p></li><li><p>You are enthusiastic to learn new skill sets, including multiplex IHC, complex image analysis, and performing cell culture </p></li><li><p>You are detail-oriented, have strong time management skills, and appreciate an opportunity for growth as a scientist.</p></li><li><p>You possess the drive and desire to learn how to troubleshoot and think outside the box to solve complex problems.</p></li><li><p>You have excellent written and verbal communication skills, and the ability to work as part of a diverse team.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><p>A BS with 7 years or MS with + 5+ years of laboratory experience (in academia or industry) in a relevant scientific discipline (Immunology, Oncology, Molecular/Cell Biology) and direct hands-on experience executing histology and immunohistochemistry techniques. Experience with autostainer platforms (e.g., Ventana or Biocare) is a plus. Experience in the research and development of targeted cancer therapeutics, including antibodies and CAR-T cells, is an advantage. The ideal candidate will possess strong organizational skills including the ability to manage and record details of several complex projects simultaneously. A demonstrated ability to communicate seamlessly and work across diverse groups to achieve a common goal is also desired.<br><br> </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>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 20:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Marketing - HCP+DTC (Dermatology)]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45693]]></requisitionid>
    <referencenumber><![CDATA[R45693]]></referencenumber>
    <apijobid><![CDATA[r45693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45693/director-marketing-hcpplusdtc-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[<p>The Director of Marketing (DTC + HCP), US Dermatology is responsible for leading, developing and completing comprehensive US digital marketing strategies to reach, educate, and activate consumers and HCPs across the omnichannel ecosystem, including web, social media, influencer, paid media, and CRM, carried out in collaboration with the Dermatology alliance team. The Director formulates and fosters innovation to provide optimal patient and customer experience. This role requires a strategic and creative problem solver with a deep understanding of bio/pharmaceutical brand marketing, digital and omnichannel marketing trends, and online consumer/HCP behavior. This role will report to the Senior Director of Dermatology Consumer Marketing.</p><h3><strong>A Typical Day Might Look Like this:</strong></h3><ul><li>Lead the development of the Dermatology Omnichannel Marketing strategy (DTC and HCP) within the overall brand strategy across all current and future Dermatology indications</li><li>Plan, develop, and help execute branded, unbranded, and multi-cultural digital consumer and NPP marketing initiatives across various online channels, including but not limited to web, social media, display, SEM, CRM, email. Includes supporting and sponsoring materials through joint medical, regulatory, and legal review committees </li><li>Own end-to-end social media strategy and activation for DTC, architecting a first-in-class influencer model and scaling integrated paid and owned programs to accelerate patient demand and optimize ROI</li><li>Lead and mentor consumer and HCP digital marketing/NPP professional(s), fostering a collaborative and innovative work environment</li><li>Demonstrated leadership experience managing direct report(s), fostering a collaborative working environment</li><li>Partner with alliance media to develop efficient and effective media mix strategies</li></ul><h3><strong>This Position Might Be for You if:</strong></h3><ul><li>You bring Strategic, scientific, and analytical competence focused on delivering results</li><li>You can demonstrate leadership and experience managing direct report(s).</li><li>You bring brand marketing experience, with expertise in DTC/HCP media and ROI analysis </li><li>You can demonstrate competency and tenured experience in social media marketing channels (influencer activation a plus)</li><li>You can focus on execution and manage multiple projects in a fast-paced environment.</li><li>You have organizational agility and the capability to reprioritize based on external or internal changes.</li><li>You can manage external partners like agencies.</li></ul><p>To be considered you must have a bachelor’s degree is required; an MBA is a plus. 12+ years of “progressive” industry/relevant professional experience in strategic roles. 8+ years of experience in pharmaceutical/biotech marketing or a related industry, including consumer/HCP brand marketing/franchise management and omnichannel strategy, with strong understanding of digital marketing trends and innovations. Experience navigating and managing alliance partnerships is preferred. Must be willing to travel 20% of the time, including weekend travel as needed. Willingness to work in a hybrid environment with a minimum of 4 days on-site at Sleepy Hollow, NY</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist]]></title>
    <date><![CDATA[Thu, 26 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46013]]></requisitionid>
    <referencenumber><![CDATA[R46013]]></referencenumber>
    <apijobid><![CDATA[r46013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46013/senior-associate-scientist/]]></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>Regeneron's Assay Development Group (ADG), located in Tarrytown, NY, is seeking a highly motivated <strong>Senior Associate Scientist</strong> to join the team. The ADG in Bioanalytical sciences develops preclinical and clinical assays to support program pipeline. In this role, you will support ongoing work, sample preparation, assay runs, data processing ensuring compliance with current GxP guidance documentation.</p><p><strong>A typical day might include:</strong></p><ul><li><p>Designs and executes immunoassays (e.g., ELISA) with minimal supervision, based on protocols provided by literature, seminars and other scientists. Troubleshoots assay-related problems with minimal guidance of his/her supervisor and performs follow-up experiments. Suggests modifications to protocols or alternative protocols.</p></li><li><p>Develops immunoassay methods and writes assay validation protocols for review with minimal supervision by supervisor and/or Study Director.</p></li><li><p>Routinely multi-tasks and can work on multiple projects simultaneously.</p></li><li><p>Summarizes and presents results to supervisor in a logical manner, verbally and in written reports or presentations.</p></li><li><p>Expertly performs validation experiments, summarizes results in a tabular manner. Writes/reviews validation reports and procedure documents for review by the Study Director.</p></li><li><p>Communicates effectively with supervisor and other members of the Assay Development Group.</p></li></ul><p><strong>This Role Could Be a Great Fit If You Have Experience:</strong></p><ul><li><p>Overseeing the preparation of reagents and buffers for use within the Assay Development Group and may coordinate the re-ordering of laboratory supplies and reagents when needed.</p></li><li><p>Effectively operating a range of laboratory instrumentation and may oversee instrument verifications and/or maintenance, if required.</p></li><li><p>Evaluating new technologies for the development of immunoassays using new formats or techniques.</p></li><li><p>Maintain GLP compliance for all laboratory work and documentation related to assay validations in accordance with FDA regulations and company SOPs. Assists in maintaining GLP compliance in the laboratory.</p></li><li><p>Maintain cleanliness of individual and communal work areas.</p></li><li><p>Learn and comply with safety requirements of his/her laboratory. Recognizes potential safety problems and takes action to correct them.</p></li></ul><p><strong>In order to be considered for this role, </strong>the individual must have Bachelor or Master degree in biology or a related field with 3-6+ years of proven experience. Hands-on knowledge in immunoassays using a variety of detection systems and a proven understanding of additional methodologies to measure proteins and immunogenicity is needed. Prior experience in bioanalytical assay development is highly desirable.</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>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Mar 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Global Procurement- Research Services]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41683]]></requisitionid>
    <referencenumber><![CDATA[R41683]]></referencenumber>
    <apijobid><![CDATA[r41683]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41683/manager-global-procurement-research-services/]]></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>As a Manager, Global Procurement, you will support the contracts with external research facilities (universities, institutions), licensing agreements, consultant agreements supporting a variety of developmental capabilities. We work closely with Discovery Research through pre-Clinical Development managing discussions related to the research and pre-clinical service contracts and aligning priorities with Procurement management and interested parties.</p><p><strong>A typical day may include the following</strong><br>• Manages complex contracts/contracting, supplier and partner activities.<br>• Work closely with stakeholders to manage discussions related to various research service categories, and aligns category priorities with Procurement management and stakeholders.</p><p>Takes direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings.<br>• Participate in organizational decisions in the research and pre-clinical service contracts with critical short and long-term impact on success, efficiency, growth, and results. <br>• Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry. <br>• Manages contract activities to ensure compliance with appropriate GxPs and other applicable regulations. <br>• Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.<br>• Uses data to drive decision-making for successful contract projects.<br>• Coaches proficiency on procurement technical skills among global procurement team.</p><p><strong>This may be for you if you:</strong><br>• Enjoy working on complex research contracts<br>• Demonstrated success working with academic institutions for pre-clinical and/or early clinical research projects<br>• Want to have an impact on patient lives<br>• Operate with integrity, focus, and clarity in an environment of ambiguity to drive change and continuous improvement.</p><p>The role requires a bachelor's degree in a relevant field of study including experience in Pharma/BioPharma and 6+ years of relevant experience within procurement. Advanced level proficiency using negotiations and contracting skills. Experience successfully managing contract processes, including strategy development and execution. Provide insight and knowledge regarding rates, unit costs, costing structures, cost models, and TCO to enable optimal negotiations. <br> </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>$113,100.00 - $184,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Flow Cytometry]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44331]]></requisitionid>
    <referencenumber><![CDATA[R44331]]></referencenumber>
    <apijobid><![CDATA[r44331]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44331/associate-scientist-flow-cytometry/]]></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 highly motivated<strong> Associate</strong> Scientist – Flow Cytometry to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as data analysis using various flow cytometric software programs.</p><p><strong>As an Associate Scientist – Flow Cytometry, A Typical Day Might Include:</strong></p><ul><li><p>Ensuring proper maintenance, alignment, and calibration of cell sorting equipment</p></li><li><p>Analyzing flow cytometric data</p></li><li><p>Maintaining and organizing schedules for cell sorting equipment</p></li><li><p>Maintaining adequate inventory of flow cytometry supplies and reagents</p></li><li><p>Supporting maintenance of flow cytometry equipment, such as LSRFortessa X-20, FACSymphony A3/A5, FACSDiscovery A8, Aurora, CytoFLEX (LX), IntelliCyt iOue, and Amnis ImageStreamX MkII cytometers</p></li><li><p>Operating a Sony MA900, FACSFusion, FACSymphony S6, and FACSDiscovery S8 high-speed cell sorters</p></li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li><p>You are able to critically analyze and troubleshoot scientific problems</p></li><li><p>You have a customer-centric viewpoint</p></li><li><p>You have good scientific initiative and ability to multi-task, prioritize work and balance multiple projects</p></li><li><p>You can work independently but also within a collaborative team environment and have flexibility to work on changing priorities</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS in a scientific field and 1-3 years of relevant experience using cytometric instrumentation. Experimental laboratory work and cytometry sorting is strongly preferred. Must be flexible and willing to perform flow cytometric duties that expedite and support scientific staff's flow cytometric goals and objectives. Experiences with cell sorting, tissue culture, cytometry staining, assay development, and data analysis is advantageous. Additionally, we need someone with analytical problem-solving experience. Cover letter is encouraged.</p><p><strong>#regncyto</strong></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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 14:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Bioinformatics]]></title>
    <date><![CDATA[Sun, 29 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46249]]></requisitionid>
    <referencenumber><![CDATA[R46249]]></referencenumber>
    <apijobid><![CDATA[r46249]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46249/senior-scientist-bioinformatics/]]></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 Molecular Profiling and Data Science Department is looking for an enthusiastic and motivated Computational Scientist who values independent research in an open and collaborative working environment. You will participate in original studies that span from basic research to translational studies, directly impacting the lives of patients.</p><p>You will join a diverse and inspiring team which leverages bioinformatic strategies to optimize key aspects of gene therapeutic products, including expression, stability, splicing, and translation. You will work closely with the Regeneron Genetic Medicines Technology Center (RGM) to advance therapeutic development through cutting-edge computational support. You will utilize genomic and transcriptomic profiling sequencing tools to engineer delivery vehicles, evaluate therapeutic cargo efficacy, and identify the off-target effects of the delivered payload.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead computational on-target and off-target characterization of gene therapy programs, utilizing both empirical NGS datasets and <em>in silico</em> prediction models.</p></li><li><p>Build and refine models to predict, score, and prioritize therapeutic off-target effects across the transcriptome and genome.</p></li><li><p>Use computational approaches to optimize expression of therapy payloads (siRNA, shRNA, snRNA and microRNA) and delivery of viral and non-viral vehicle technologies.</p></li><li><p>Develop internal tools, pipelines, workflows, and documentation that raise the analytical standards of the Molecular Profiling and Data Science group.</p></li><li><p>Contribute with technical expertise on discussions of research efforts conducted by your and other departments in the company.</p></li><li><p>Prepare and deliver clear, concise scientific presentations for collaborators and senior management.</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Have a strong background in gene therapy and differential gene expression analysis.</p></li><li><p>Have direct experience or is very familiar with the production of a range of NGS datasets.</p></li><li><p>Bring innovative thinking to multi-omics data analysis.</p></li><li><p>Have a strong work ethic and are proactive in providing solutions to foster scientific collaborations and drive projects forward within Regeneron.</p></li><li><p>Can effectively communicate with collaborators of various scientific backgrounds.</p></li><li><p>Value teamwork and team excellence.</p></li></ul><p><strong>In order to be considered for this role, you must have</strong>:</p><ul><li><p>Ph.D. in Data Science, computational biology, or related field</p></li><li><p>0-2 years of relevant experience</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 30 Mar 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Biologics Characterization]]></title>
    <date><![CDATA[Sun, 29 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45974]]></requisitionid>
    <referencenumber><![CDATA[R45974]]></referencenumber>
    <apijobid><![CDATA[r45974]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45974/associate-scientist-biologics-characterization/]]></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>Regeneron is seeking a highly motivated and passionate Associate Scientist to join our Protein Biochemistry team. In this exciting role, you will play a critical part in implementing innovative biophysical assessment strategies to support a wide range of drug candidate modalities.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li>With supervisory direction and support, conducts biochemical and biophysical characterization experiments on therapeutic protein for late-stage development and regulatory submissions. </li><li>Provide input on experimental design and suggest modifications in protocols or methods to meet the needs of a particular program or molecule. </li><li>Will take on additional responsibilities in advanced method development to support efforts to enrich and characterize size/charge variants, protein-ligand complexes, and high concentration protein solutions of therapeutic protein drug candidates. </li><li>Documents experiments, results and findings in electronic laboratory notebook in a timely manner; presents work at group and department meetings; contributes to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication.</li><li>Maintain instruments, troubleshoot instrumental/experimental problems, and order/maintain supplies. Keen to follow procedures, guidance, and best practices for lab safety.</li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li>You have initiative and drive to complete meaningful tasks and learn new technologies.</li><li>You can work both independently and within a team environment on projects simultaneously</li><li>You contribute to lab equipment maintenance and safety to help create a safe, effective and efficient working environment.</li><li>You possess strong organizational, communication, analytical, computer, and technical writing skills.</li></ul><p>This role requires a BS/MS in Biochemistry/Biophysics, or related field plus 0-3 yrs+ experience. Technical proficiency in automated FPLC and/or HPLC (SEC, IEX, affinity), electrophoresis (capillary or microchip, SDS-PAGE, western blots), spectroscopy and light scattering is recommended. A fundamental understanding of protein structure/function, protein-protein interaction and general biochemistry preferred. Preference will be given to candidates who have experience working in the biopharmaceutical industry. Excellent oral and written communication skills and evidence of teamwork are required.</p><p>The ideal candidate must have strong initiative to complete tasks, learn new technologies, and demonstrate a commitment to continuous learning. This role requires the ability to manage multiple priorities in a fast‑moving R&D environment, operate effectively both independently and within a collaborative team environment, and communicate clearly, transparently, and in a timely manner with key stakeholders.</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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 30 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46271]]></requisitionid>
    <referencenumber><![CDATA[R46271]]></referencenumber>
    <apijobid><![CDATA[r46271]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46271/associate-scientist/]]></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 Scientist </strong><strong>(Tarrytown, NY)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks an Associate Scientist (Tarrytown, NY) to conduct laboratory experiments supporting the design, development, and functional validation of gene therapy platforms, gene editing technologies, novel viral vectors, and nucleic acid therapeutics targeting neurological and neurodegenerative diseases. Support technology development for antibody-based strategies to improve targeted drug delivery across the blood brain barrier (BBB), to the CNS and into specific tissues and cell types of interest. Plan and perform experiments to functionally validate novel targeted drugs (siRNAs, ASOs, shRNAs, CRISPR systems, vectorized antibodies or peptides) and viral vectors in in vitro models. Perform cell culture with immortalized cell lines, iPSC-derived cells and primary cultures, and cell-based assays (ICC, flow cytometry). Plan, initiate, and complete molecular biology and biochemistry assays: molecular cloning, PCR, RT-qPCR, RNA sequencing, ELISAs, IP, WB, CE-western. Perform advanced data analysis (Halo, ImageJ, FlowJo, Prism) and troubleshooting under minimal supervision. Keep up-to-date and well-organized records of experimental protocols and results. Communicate and report experimental findings at group and departmental meetings. Survey current and relevant literature to expand scientific and technical knowledge and optimize and develop new assays.</p><p>SALARY RANGE: $74,838.00 - $110,100.00 per year</p><p><strong>Job Requirements:</strong></p><p>Requires a Bachelor’s degree in Biology, Neuroscience, Clinical Research, or a related field, and 1 year of in vitro lab experience. Must have experience with: Neuroscience, molecular tools for CNS targeting, in vitro models of neurodegenerative disorders; Aseptic technique and culturing various in vitro cell lines such as HEK293T and primary neurons; Working with iPSC-derived cells with knowledge in differentiation protocols to generate iPSC-derived neurons and other CNS cell types; Generating lentivirus and leveraging them to generate stable cell lines in vitro; Cell-based assay techniques, including immunocytochemistry/immunofluorescence (ICC/IF) and flow cytometry; Molecular biology techniques and biochemical assays, including cloning, sequencing, PCR, RT-qPCR, ELISA, immunoprecipitation, and western blot; and Data analysis using ImageJ, Prism, and sequence alignment tools.</p><p>Apply at https://careers.regeneron.com; Reference code: R46271.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Fill/Finish Associate (Internal Fill/Finish MFG)]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46367]]></requisitionid>
    <referencenumber><![CDATA[R46367]]></referencenumber>
    <apijobid><![CDATA[r46367]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>We are currently looking to fill 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><br>As a Fill/Finish Associate, a typical day might include the following:</p><ul><li><p>Produces life-saving therapeutics for various indications developed from a dynamic internal pipeline</p></li><li><p>Works with a team that is accountable for production activities ranging from formulation of drug product to packaging of final drug product, which may include the following process-related responsibilities:</p></li><li><p>Operates highly automated equipment to fill drug product into vials or syringes within isolators or other aseptic environments</p></li><li><p>Assembles filled drug product into syringes and autoinjectors</p></li><li><p>Operates state of the art packaging lines to place assembled and labeled drug product into packaging configurations for distribution</p></li><li><p>Monitors production line for proper operation through process controls including pneumatics, robotics, manual and PLC feedback loop systems</p></li><li><p>Cleans, handles, and installs interchangeable parts for various systems and equipment</p></li><li><p>Collaborates to create and maintain operating procedures to perform routine activities that adhere to regulatory expectations</p></li><li><p>Ensures working spaces and equipment are clean, safe, and ready for processing activities</p></li><li><p>Maintains gowning qualification and adheres to clean room behaviors wherever required</p></li><li><p>Performs environmental sampling using various methods where applicable</p></li><li><p>Records GMP data that is accurate, legible, attributable, and contemporaneous and completes review on those records</p></li><li><p>Maintains and ensures proper documentation of all training</p></li><li><p>Navigates and utilizes electronic systems to support manufacturing operations</p></li><li><p>Travel (domestic and international) may be required.</p></li><li><p>Ensures compliance with applicable procedures while executing activities and escalates any non-conformities during operations</p></li><li><p>Performs reconciliation of product and controlled materials where applicable</p></li></ul><p>This role might be for you if:</p><ul><li><p>Ability to perform basic algebra and geometry</p></li><li><p>Reading/writing skills</p></li><li><p>Must be able to stand for extended periods of time and lift, push and pull at least 50lbs.</p></li><li><p>Knowledge of cGMP and FDA regulated (preferred) manufacturing environment and familiarity with cGMP filling, assembly or packaging processes preferred.</p></li><li><p>Necessary to have keen attention to detail and demonstrate from previous work experiences.</p></li><li><p>Preferred experience with aseptic technique and operating filling equipment or with assembly or packaging of parenteral products in vials, syringes and cartridges using both manual and automated equipment preferred.</p></li><li><p>Basic understanding of Microsoft Office Suite.</p></li><li><p>Demonstrates strong interpersonal, cross-cultural, communication, negotiation and has a high emotional IQ.</p></li><li><p>Exhibits confidence and strong problem-solving skills and demonstrates ingenuity, creativity and resourcefulness.</p></li><li><p>Gains understanding from provided instructions and works towards established goals.</p></li><li><p>Understands and listens to team members and stakeholders’ needs while supporting a positive team environment.</p></li><li><p>Possess a strong and effective communication style among peers and with management team</p></li><li><p>Values and acts with integrity</p></li></ul><p>Shift Requirements: Physical</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours):</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>Gowning and Environment</p><ul><li><p>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><br>To be considered for the Fill/Finish Associate you must have a GED/High School diploma and previous work experience.</p><p><em>Level is figured out based on qualifications relevant to the role. </em></p><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 (hourly)</strong></strong></p>$16.44 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Facilities Maintenance Specialist - EAMS Administrator]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43340]]></requisitionid>
    <referencenumber><![CDATA[R43340]]></referencenumber>
    <apijobid><![CDATA[r43340]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43340/facilities-maintenance-specialist-eams-administrator/]]></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 seeking a Maintenance Specialist - EAMS Administrator to join our Facilities department. This role will serve primarily as the Enterprise Asset Management System (EAMS) Administrator supporting the facilities department.</p><p>As a Maintenance Specialist, a typical day might include:</p><ul><li><p>Maintaining master data (system level data), bulk data updates, and overseeing change control for Maximo configurations and data updates.</p></li><li><p>Supporting new site deployments and updates for Maximo including data preparation, system site setup, data import, and end user training.</p></li><li><p>Working with maintenance teams to develop new, and improve existing, maintenance strategies.</p></li><li><p>Coordinating maintenance activities for GMP and non-GMP equipment.</p></li><li><p>Ensuring completion of all documentation in compliance with site procedures and GDP.</p></li><li><p>Developing and maintaining reports for compliance, maintenance KPIs, and asset performance.</p></li><li><p>Supporting IT in the implementation of EAMS upgrades and configuration changes.</p></li><li><p>Supporting deviation investigations, CAPAs, and change controls related to equipment and maintenance.</p></li><li><p>Regularly interacting with Facilities, Manufacturing, Quality Assurance, Validation, and Engineering teams.</p></li><li><p>Ensuring the safe accomplishment of daily activities within the maintenance department, while following all site and department practices and procedures.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have hands-on experience with IBM Maximo or similar EAM/CMMS.</p></li><li><p>Have experience in EAMS Administration and/or maintenance activities within a GMP regulated environment (preferred).</p></li><li><p>Are adept at collaborating with cross-functional teams and communicating effectively with partners.</p></li><li><p>Are detail-oriented with excellent organizational skills and the ability to manage multiple priorities.</p></li><li><p>Possess strong data management and reporting skills.</p></li></ul><p>To be considered for this position you should have a BS/BA in a relevant field or equivalent combination of education and experience along with the following minimum years of experience in maintenance, facilities, or asset management in a regulated industry for each level.</p><ul><li><p>Maintenance Specialist: 2+ years</p></li><li><p>Senior Maintenance Specialist: 5+ years</p></li></ul><p>Level will be determined based on qualifications relevant to the role</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>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Patient & Channel Data Management]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46284]]></requisitionid>
    <referencenumber><![CDATA[R46284]]></referencenumber>
    <apijobid><![CDATA[r46284]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46284/associate-director-patient-channel-data-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>The Associate Director, Patient and Channel Data Management will report into Director, Patient and Channel Data Management within the Commercial Strategy and Insights and Analytics (CSI&A) department. </p><p><strong>In this role, a typical day might include:</strong></p><p>The Associate Director, Patient and Channel Data management is responsible for the curation, governance, quality and operationalization of patient/specialty data assets that power commercial decision making across therapeutic areas. The ideal candidate brings deep expertise in specialty pharmaceutical data ecosystems, strong problem-solving capabilities, and the ability to influence and drive alignment across a broad set of cross-functional partners.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><ul><li><p>Serve as the subject matter expert and strategic owner for channel and patient support services data assets; develop and maintain data management frameworks, SOPs, data dictionaries, and data maps across all relevant data domains</p></li><li><p>Establish and monitor data quality metrics to ensure accuracy, completeness, and integrity; drive root cause analysis and resolution of data quality issues, including SP/SD/patient-level data reconciliation</p></li></ul><p><em>Develop</em></p><ul><li><p>Support integration of specialty data into commercial reporting, forecasting, and analytics platforms; maintain alignment with enterprise data governance principles in partnership with governance teams</p></li><li><p>Contribute to launch readiness by building data infrastructure and reporting frameworks ahead of new product or indication launches; represent the data management function in commercial operations working groups and leadership reviews</p></li></ul><p><em>Partnership and Collaboration</em></p><ul><li><p>Provide accurate channel-level data inputs to support gross-to-net and revenue deductions modeling in partnership with Trade and Market Access teams</p></li><li><p>Manage relationships with data aggregators, specialty distributors, SP data providers, and PSS vendors, including contract scope, data delivery SLAs, issue escalation, and regular business reviews</p></li><li><p>Serve as a key data management partner across internal stakeholders (PSS, Trade, CIT, I&A Market Access, Advanced Analytics), translating complex data concepts into clear business context for non-technical audiences</p></li></ul><p><em>Execute</em></p><ul><li><p>Manage end-to-end data flows from specialty distributors and specialty pharmacies, including SD 867/852 transaction data, SP inventory and dispense, chargeback, and ex-factory shipment data</p></li><li><p>Build, manage and govern PSS data assets across the full patient journey (patient intake, BI/BV, eBV, PA/ePA, copay enrollment/claims, free goods/PAP/IAP) in strict compliance with HIPAA, PHI requirements, and Regeneron data governance and tokenization standards</p></li><li><p>Maintain working knowledge of and leverage industry-standard commercial datasets (IQVIA LAAD, APLD, Symphony Health, Precision, MMIT); apply data tokenization methodologies to link patient-level data across sources while maintaining PHI compliance</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>BA/BS with 10+ years (or MBA/MS with 7+ years) of experience in commercial data management, analytics, or operations within the pharmaceutical or biotechnology industry</p></li><li><p>Deep expertise in patient/specialty pharmaceutical data ecosystems, including: Deep expertise in specialty pharmaceutical data ecosystems, including channel/trade data (SD 867/852, SP inventory/dispense, chargeback, ex-factory), SP/SD reconciliation and audit controls, and PSS data (patient intake, BI/BV, eBV, PA/ePA, copay enrollment/claims, free goods, IAP/PAP)</p></li><li><p>Strong working knowledge of industry-standard datasets including IQVIA LAAD, APLD, Symphony Health, Precision, and MMIT</p></li><li><p>Experience with data tokenization, PHI handling, and HIPAA compliance requirements</p></li><li><p>Proficiency with data management and analytics tools (e.g., SQL, Snowflake, Databricks, or equivalent)</p></li><li><p>Proven experience managing external data vendors and holding partners accountable to SLAs</p></li><li><p>Demonstrated ability to influence without authority and drive alignment across cross-functional teams</p></li><li><p>Demonstrated flexibility, leadership presence, and emotional intelligence when navigating complex stakeholder environments and competing priorities</p></li><li><p>Strong problem-solving skills with a structured, analytical approach to identifying and resolving data issues</p></li><li><p>Excellent written and verbal communication skills; ability to translate complex data concepts for diverse audiences</p></li><li><p>Experience supporting an ophthalmology, retina, or other specialty/rare disease commercial franchise (Preferred)</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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs Strategy - Immunology & Inflammation]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46317]]></requisitionid>
    <referencenumber><![CDATA[R46317]]></referencenumber>
    <apijobid><![CDATA[r46317]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46317/manager-regulatory-affairs-strategy-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 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><strong>A typical day might include the following:</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 might be for you:</strong> </p><ul><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><p><strong>To be considered for this opportunity</strong>, we expect you must have a MD, PhD or PharmD degree along with 2+ years of regulatory experience. We expect to see individuals have worked on filings, helped with developing regulatory related documents and engaged with external partners and authorities. </p><p>#GDRAJobs</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>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 15:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal GMP Data Governance Business Partner (Data Integrity)]]></title>
    <date><![CDATA[Tue, 20 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R36336]]></requisitionid>
    <referencenumber><![CDATA[R36336]]></referencenumber>
    <apijobid><![CDATA[r36336]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r36336/principal-gmp-data-governance-business-partner-data-integrity/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will be responsible for the implementation of data governance (DG) standards, policies and procedures into business operations. You will be a site expert on Data Governance, supporting the Regeneron IOPS Data Governance and Integrity program.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Implementing the Data Governance standards, policies and procedures within allocated areas of the business</p></li><li><p>Being the allocated business area(s) key DG contact providing support and advice and engage with the allocated business unit on DG priorities and action plans</p></li><li><p>Assessing allocated business unit’s current policies and processes and coordinate the achievement of local KPIs</p></li><li><p>Conducting regular data audits and assessments to identify DG issues and work with business area to prepare for DG auditing and inspections</p></li><li><p>Working with DG Business Partners, Technical Experts, and ECM Experts to deliver the DG plan and provide feedback for continuous improvement</p></li><li><p>Encouraging a culture of quality and Data Governance within the organisation and promoting the importance of DG across all departments</p></li><li><p>Driving communication and collaboration between stakeholders to ensure effective DG practices</p></li><li><p>Encouraging continuous improvement by actively seeking feedback and supporting initiatives designed to improve data quality and governance</p></li><li><p>Leading/supporting initiatives to embed DG principles into the company’s core values and everyday practices</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You have knowledge of relevant regulations and guidelines (e.g., GDPR, FDA, EMA, WHO)</p></li><li><p>You have proven success in implementing and managing policies in regulated environments</p></li><li><p>You bring strong communication and collaboration skills</p></li><li><p>You are skilled in stakeholder management and influence</p></li><li><p>You have experience with quality systems and change management</p></li></ul><p>To be considered for this role you must hold a BA/BS degree and 7+ years of professional experience or equivalent combination of education and experience in pharmaceutical/FDA regulated work areas such as: data management & operations, quality assurance, compliance, manufacturing operations, quality control, or IT.</p><p>#LI-Onsite #JOBSIEST #IRELIM #REGNIRLTO </p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 21 Jan 2026 08:56:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists  - Hematology - Orange County, Duarte, Inland and Empire to San Diego CA]]></title>
    <date><![CDATA[Sun, 25 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44693]]></requisitionid>
    <referencenumber><![CDATA[R44693]]></referencenumber>
    <apijobid><![CDATA[r44693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44693/medical-account-specialists-hematology-orange-county-duarte-inland-and-empire-to-san-diego-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>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>A typical day may include the following:</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 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><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 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><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>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 26 Jan 2026 15:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, AI Engineering (Global Development)]]></title>
    <date><![CDATA[Wed, 04 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44760]]></requisitionid>
    <referencenumber><![CDATA[R44760]]></referencenumber>
    <apijobid><![CDATA[r44760]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44760/director-ai-engineering-global-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>Our Global Development (GD) team is seeking a Director, AI Engineering to embark on a digital transformation incorporating AI, machine learning, and automation. The goal is to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. You will play a key role in developing platforms, processes and technologies across GD. </p><p><strong>A typical day may include the following: </strong><br>• Provide strategic direction and technical leadership to an eventual team of engineers to design, implement, and refine novel algorithms and scalable AI /ML solutions. These will be tailored to applications such as clinical trial design, regulatory intelligence, patient identification and stratification. Oversee the deployment of these solutions into production environments, employing hands-on technical expertise to ensure excellence in execution.<br>• Architect and refine data engineering and data architecture strategies to integrate and optimize diverse data sources. <br>• Partner with the Digital Transformation AI lead and leaders across Global Development to evaluate and implement use cases for implementing AI in the enterprise, including automating manual processes such as protocol review, monitoring, and adverse event review<br>• Provide strategic leadership to initiatives with Global Development IT and enterprise IT to building infrastructure (software and hardware) to support advanced analytics, including vendor evaluation<br>• Collaborate with senior leaders to identify high-value opportunities for AI/ML integration and lead the execution of innovative solutions that address critical business challenges.<br>• Empower colleagues to leverage AI/ML effectively by providing guidance that bridges technical expertise with strategic insights, fostering a culture of innovation and continuous learning.<br>• Establish robust validation frameworks for AI models, ensuring reliability and efficiency<br>• Stay at the forefront of AI/ML advancements, evaluating emerging technologies and methodologies for potential adoption within Regeneron.<br>• Lead initiatives to continuously improve the organization's AI capabilities, fostering a competitive edge. </p><p><strong>This may be for you if you: </strong><br>• Want to be a part of scaling AI in a growing multi-national organization. <br>• Can demonstrate managing cross functional teams. <br>• Demonstrated success bringing transformative change. <br>• Want to have an impact on patient lives<br>T</p><p>o be considered you are to have a PhD in Computer Science, Data Science, AI/ML, Engineering, or related with 10-12 years experience or a Master or Bachelor’s with 12–15+ years experience in AI?ML or software engineering. Your experience must include a deep understanding of generative AI, machine learning, natural language processing, and statistical modeling. Expertise in programming (Python, R, etc.), with a focus on applying advanced technical skills to data analysis, automation, and software development is required. Expertise in database platforms and cloud computing infrastructure. Experience managing and analyzing large-scale clinical datasets Excellent communication skills, including experience presenting to senior leadership, both technical and non-technical. Experience managing multiple projects in parallel. Experience working in and managing cross-functional teams. Have track record of model development, implementation to scale, maintenance, and evaluation in a healthcare of life sciences setting<br> May require travel up to 20%. <br> </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>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Feb 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Animal Production - Velocigene]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44048]]></requisitionid>
    <referencenumber><![CDATA[R44048]]></referencenumber>
    <apijobid><![CDATA[r44048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44048/director-animal-production-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>As a leader, the Director of Animal Production drives strategic growth of VelociGene’s genetically engineered mouse (rodent) models (GEMM), and pursues R&D portfolio support across departments. This role addresses challenges across functional areas of the business and is responsible for the successful operation of activities of major significance to the organization involving GEMM developed by VelociGene.</p><h3>Strategic Impact</h3><p>The Director of Animal Production plays a critical role in advancing Regeneron’s R&D objectives by driving strategic goal setting, portfolio management, and ensuring timely, cross-functional coordination for the delivery of mouse models that enable project progression within the R&D pipeline. An understanding of pharmaceutical R&D portfolio strategy is essential to effectively prioritize vivarium resources and accelerate GEM model development.</p><p>Key priorities include standardizing processes and procedures, proactively identifying and resolving issues, and fostering operational excellence. As Director, you will continue the building of a large, high-performing, quality-focused organization that embraces innovation and continuous improvement. Decisions made in this role directly influence Regeneron’s ability to achieve its research goals, requiring a commitment to change management and to a culture that prioritizes leadership and talent development.</p><p>This position includes supervisory responsibilities,</p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li>Drive operational strategy for model development, ensuring efficiency, compliance, and scientific rigor.</li><li>Manage cross-functional collaborations to optimize timelines and resource allocation for GEM model delivery.</li><li>Implement standardized processes and quality controls to enhance reproducibility and reliability across all operations.</li><li>Champion continuous improvement and innovation, fostering a culture of accountability and adaptability.</li><li>Develop and mentor team members, building leadership capability and sustaining high performance.</li><li>Ensure effective communication and alignment across departments to support strategic objectives and organizational goals.</li><li>Supervise managers and optimizing their plans, policies, and objectives, while monitoring performance against goals</li><li>Interact internally and externally with executive-level management</li><li>Develope and maintain relationships with cross-departmental and functional stakeholders to ensure all operations are aligned with departmental and R&D initiatives.</li></ul><h3>This Role Might Be For You If You:</h3><ul><li>Have a keen understanding of pharmaceutical R&D portfolio strategy</li><li>Effectively prioritize resources and accelerate GEM model development</li><li>Have a track record of standardizing processes and procedures, proactively identifying and resolving issues, and fostering operational excellence</li><li>Embrace innovation and continuous improvement</li></ul><p>This position reports to a Vice President and requires a bachelor degree with 15 or more years of professional experience. A graduate degree (MS or PhD) or equivalent is beneficial/preferred. Experience leading a diverse multi-level team of at least 25 individuals is required. A background in vivarium operations, molecular biology, GEM model generation, and application of data systems to a GEM model pipeline is essential. Demonstrated publication or patent records are considered a plus.</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Nashville/Brentwood/Franklin, TN]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45097]]></requisitionid>
    <referencenumber><![CDATA[R45097]]></referencenumber>
    <apijobid><![CDATA[r45097]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45097/medical-specialist-i-nashvillebrentwoodfranklin-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>Geography: Nashville/Brentwood/Franklin, TN</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44896]]></requisitionid>
    <referencenumber><![CDATA[R44896]]></referencenumber>
    <apijobid><![CDATA[r44896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies.</p><p><strong>In this role, a typical day might include:</strong> ​</p><p>As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in 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. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.</p><p><strong>This role might be for you if can:</strong> ​</p><ul><li>Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. </li><li>Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. </li><li>Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).</li><li>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. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.</li><li>Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</li><li>Participate in department working groups; provide input in development of tools and improvement of processes.</li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>Masters Degree</li><li>SAS, (Base, Stat, Macro, graph). </li><li>3 + Years experience</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - South West England]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45109]]></requisitionid>
    <referencenumber><![CDATA[R45109]]></referencenumber>
    <apijobid><![CDATA[r45109]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Oracle ERP Business Program Lead]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44473]]></requisitionid>
    <referencenumber><![CDATA[R44473]]></referencenumber>
    <apijobid><![CDATA[r44473]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44473/executive-director-oracle-erp-business-program-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>The Business Program Lead is responsible for the overall management, execution, and delivery of Regeneron’s ERP Modernization Program and reports to the Program Sponsors. This role provides strategic leadership, governance, and oversight across all workstreams, ensuring alignment with business objectives and adherence to guiding principles. The Program Lead drives oversight of program planning, execution, risk management, and stakeholder engagement, while championing business-led change and adoption. Operating in a matrix environment, this role partners with Program Managers, Global Process Owners, IT leadership, System Integrators, and functional teams to deliver measurable business outcomes.</p><div></div><p><strong>A typical day in this role might look like: </strong></p><ul><li>Accountable for the integrated program plan, scope, schedule, dependencies, budget as well as alignment to the business case.</li><li>Lead governance forums (SteerCo, Design Review Board) and enforce guiding principles and key design decision (template-first, clean core).</li><li>Accountable for the execution of program deliverables; monitor progress, risks, and issues; implement mitigation plans.</li><li>Serve as primary liaison to executive sponsors; prepare and present status updates and decision requests.</li><li>Oversee vendor and SI performance; ensure deliverables meet scope, timeline, and quality standards.</li><li>Champion change management and readiness; oversee communications, training, and adoption strategies.</li><li>Ensure compliance with SOX, GxP, and audit requirements in all program activities.</li><li>Define and track success metrics; ensure benefit realization and continuous enhancements post-go-live.</li></ul><div></div><p><strong>This role might be for you if: </strong></p><ul><li>Bachelor’s degree in Business, Finance, Engineering, or related field; MBA preferred.</li><li>15+ years of experience in large-scale ERP or business transformation programs; 10+ years in program leadership.</li><li>Proven ability to manage complex, multi-year global programs with cross-functional teams and vendors.</li><li>Strong knowledge of ERP systems (Oracle Fusion preferred) and end-to-end life science business processes.</li><li>Expertise in program governance, risk management, and change leadership.</li><li>PMP or PgMP certification preferred; Iterative methodology delivery experience a plus.</li><li>Exceptional communication, stakeholder management, and leadership skills.</li><li>Willingness to travel up to 25%.</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 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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist-Dermatology-Los Angeles North]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44982]]></requisitionid>
    <referencenumber><![CDATA[R44982]]></referencenumber>
    <apijobid><![CDATA[r44982]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44982/medical-specialist-dermatology-los-angeles-north/]]></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>Medical Specialist, Dermatology- Los Angeles North (MS)</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. 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. We need someone with proven success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Ft. Myers, FL]]></title>
    <date><![CDATA[Tue, 10 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45103]]></requisitionid>
    <referencenumber><![CDATA[R45103]]></referencenumber>
    <apijobid><![CDATA[r45103]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45103/medical-specialist-i-dermatology-ft-myers-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cape Coral]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Ft. Myers, FL</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><p>.</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I- Dermatology- Boise, ID]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44953]]></requisitionid>
    <referencenumber><![CDATA[R44953]]></referencenumber>
    <apijobid><![CDATA[r44953]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44953/medical-specialist-i-dermatology-boise-id/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Boise City]]></city>
    <state><![CDATA[Idaho]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Boise, ID (also covers Spokane WA and Western MT)</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>As a Medical Specialist, a typical day may include the following:</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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety]]></title>
    <date><![CDATA[Sun, 15 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45330]]></requisitionid>
    <referencenumber><![CDATA[R45330]]></referencenumber>
    <apijobid><![CDATA[r45330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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[<p><strong>Position Overview</strong></p><p>Our mission is to safeguard patient safety and lead pharmacovigilance (PV) in Japan.</p><p>The Senior Manager, Global Patient Safety (GPS) reports to the Director, GPS (Safety Management Officer) in Japan and serves as a core leader for safety operations, overseeing the handling of Individual Case Safety Reports (ICSR), Investigation Reports (RR), and Foreign Measures Taken (FSMT) reports. Additionally, this role proactively drives aggregate reporting, vendor management, and GVP-related activities to ensure both quality and compliance.</p><p><strong>What Makes This Role Attractive</strong></p><ul><li>Make meaningful impact in a high-stakes safety function as a key member driving Japan’s PV framework</li><li>Lead vendors and cross-functional teams to design and implement process improvements</li><li>Contribute to pivotal documents directly linked to development and post-approval, including J-RMP and J-NDA</li><li>Collaborate globally and gain experience bridging international standards with Japanese regulations</li><li>Build your career through audits and inspections exposure and by managing complex, high-impact projects</li></ul><p><br><strong>Responsibilities</strong></p><ul><li>Serve as Japan’s point of contact for ICSR, RR, and FSMT handling, ensuring quality and on-time delivery</li><li>Lead local aggregate reporting and ensure submissions meet regulatory requirements</li><li>Monitor and oversee PV service providers, ensuring performance aligns with contracts and project plans</li><li>Review provider-prepared assessments and PMDA reports for accuracy and execute improvement actions</li><li>Design and drive continuous process improvements to enhance quality and compliance</li><li>Lead creation and revision of SOPs and plan/execute related training as needed</li><li>Contribute to Japan Risk Management Plan (J-RMP) development and manage planning, execution, and tracking</li><li>Partner effectively with internal cross-functional teams (Medical Affairs, Regulatory Affairs, Commercial/Marketing, Clinical Development) and license partners to ensure the quality and alignment of PV deliverables</li><li>Contribute to the safety section of the Japan New Drug Application (J-NDA) and lead resolution of PMDA inquiries</li></ul><p><br><strong>Qualifications</strong></p><ul><li>7+ years of hands-on experience in drug safety/pharmacovigilance within the pharma/biotech industry</li><li>Strong knowledge of PMDA/MHLW/ICH guidelines and regulations governing PV in both clinical trials and post-marketing settings</li><li>Proven track record of delivering results through cross-functional collaboration with Medical Affairs, Regulatory Affairs, Commercial, and Clinical Development</li><li>Experience supporting or leading regulatory authority audits/inspections, including PMDA re-examination, MAH license renewal, and GCP reliability inspections</li><li>Project management experience in complex initiatives such as safety database implementations, function/team improvements, and transfers of business authorizations (including safety data migration)</li><li>Experience in contracting and managing external service providers</li><li>Practical experience in global PV</li></ul><p><br><strong>Career Opportunities</strong></p><ul><li>Gain a panoramic view of Japan’s safety operations and participate in high-impact decision-making</li><li>Strengthen both subject-matter expertise and leadership capabilities through global collaboration and Japanese regulatory engagement</li><li>Build a resilient career through deep involvement in key deliverables such as SOPs, J-RMP, and J-NDA</li></ul><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Feb 2026 04:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Data Reporting]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45331]]></requisitionid>
    <referencenumber><![CDATA[R45331]]></referencenumber>
    <apijobid><![CDATA[r45331]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45331/associate-director-clinical-data-reporting/]]></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>The Associated Director of Clinical Data Management Reporting will provide strategic leadership for clinical and external data reporting across clinical development unit (CDU) programs. This role focuses on the creation, standardization, and delivery of clinical data programming, external data reconciliation, and reporting deliverables across portfolio, ensuring alignment with study data review plans (DRP), study milestone needs, operational metrics, and regulatory requirements. The incumbent will be accountable for the oversight and execution of all data management programming deliverables at the portfolio level. Responsibilities include quality and timely delivery of programming outputs such as data review plan listings, exception listings, external data reconciliation reports, operational metrics, and other reports supporting clinical trial quality and risk management. The Director will manage internal teams and external vendors, ensuring study milestones are met while safeguarding data quality, integrity, and compliance with global regulatory standards. The position emphasizes cross-functional collaboration, deep expertise in clinical data programming, external data handling and reconciliation, industry standards, programming methodologies, and clinical data management systems. </div><div><div><div><div><p><strong>As a Associate Director, Clinical Data Reporting, a typical day may include:</strong></p><ul><li><p>Drive strategic leadership with full accountability for the planning, execution, and delivery of high-quality clinical data management programming deliverables across the portfolio of clinical development units. </p></li><li><p>Provide comprehensive oversight of clinical programming and visualization outputs that reveal key insights to support clinical data review, including data review listings, exception listings, external data reconciliation, operational metrics, and other quality reports and ensure accuracy, reliability, and integrity of data supporting clinical studies across the portfolio.</p></li><li><p>Advance operational excellence by establishing robust data reporting standards, implementing scalable programming strategies, optimizing workflows incorporating automation, and ensuring consistent delivery of high-quality outputs in accordance with defined user requirement specifications.</p></li><li><p>Provide subject matter expertise in advanced clinical data programming, data extraction and transformation, visualization, and emerging technologies to enhance and advance internal data reporting capabilities. </p></li><li><p>Collaborate with clinical data management teams, functional line management, and cross-functional teams to align priorities, streamline workflows, optimize resource allocation, and drive successful delivery of clinical data management programming objectives. </p></li><li><p>Apply quality-by-design principles to all clinical data management programming and reporting deliverables ensuring that high-quality outputs are aligned and consistent with risk-based strategies, and inspection readiness.</p></li><li><p>Lead continuous improvement initiatives to modernize clinical data reporting workflows through standardization, process optimization, and automation to improve programming efficiency and scalability. </p></li><li><p>Proactively identify potential risks to data quality, integrity, and delivery timelines and implement mitigation strategies to ensure continuity, compliance, and successful delivery of programming objectives.</p></li><li><p>Ensure inspection readiness and regulatory compliance of programming documentation; contribute to internal audits and health authority inquiries.</p></li><li><p>Establish and monitor KPIs to track performance, conformance with programming standards, and identify opportunities to enhance and/or optimize reporting capabilities.</p></li><li><p>Responsible for line management and performance of Clinical Data Management Reporting staff, development of competencies and assessment of annual performance.</p></li><li><p>Provide leadership and mentorship to programming teams, fostering skill development, knowledge sharing, and operational excellence. </p></li><li><p>Author and contribute to the development of clinical data management programming and reporting SOPs, WIs and departmental training needs.</p></li></ul><p><strong>To be considered for this role, you must meet the following requirements:</strong></p><ul><li><p>Demonstrated ability to oversee the development, validation, and delivery of clinical data management programming and visualization outputs to cross-functional teams across drug development programs.</p></li><li><p>Experience in transforming raw clinical data, external data handling, processing, validation, and reconciliation outputs into actionable insights to ensure data accuracy and quality in compliance with industry standards.</p></li><li><p>Demonstrated ability to function as a clinical data management programming and reporting SME in solving complex issues and guiding internal teams and external vendors for successful outcomes. </p></li><li><p>Demonstrated ability to build relationships and collaborate across diverse business units including Clinical Data Management, Clinical Development, Precision Medicine, Imaging, and GDIT.</p></li><li><p>Expertise in managing and reconciling clinical eCRF and external data types including PK, ADA, Biomarker, Imaging, ECG, etc., to ensure data accuracy, integrity, and regulatory compliance. </p></li><li><p>Proven experience in clinical data operations, clinical data management, reporting, and analytics within a pharmaceutical, biotech, or clinical research organization.</p></li><li><p>Knowledge of clinical data management principles, technologies, data extraction, transformation, and integration, programming methods and techniques, regulations and best practices, including 21 CFR Part 11, ICH-GCP, and CDISC standards -- related to data acquisition, processing, handling, and reporting. </p></li><li><p>Knowledge and expertise in industry standard reporting and data visualization tools including SAS, R, JReview, Spotfire, Tableau, Power BI, and R Shiny to drive operational excellence for clinical data management reporting. </p></li><li><p>Excellent interpersonal, oral, and written communication skills.</p></li><li><p>Ability to adjust in a fast-paced environment.</p></li><li><p>May require up to 25% travel.</p></li><li><p>BS/MS </p></li><li><p>10+ years of clinical data management experience in a pharmaceutical or biotech</p></li><li><p>5+ years of people management, leadership, and mentoring experience.</p></li></ul></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>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Immunology Key Accounts Lead, Mid-West]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45135]]></requisitionid>
    <referencenumber><![CDATA[R45135]]></referencenumber>
    <apijobid><![CDATA[r45135]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45135/director-immunology-key-accounts-lead-mid-west/]]></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[<p>The Respiratory / Immunology Key Account Lead (IKAL) has a critical role in establishing Regeneron as a leader in Respiratory & Immunology spaces by serving as a strategic partner and trusted advisor to high-value Integrated Delivery Network (IDN’s) healthcare accounts. The KAL role will be instrumental to driving long-term engagement, operational excellence, and business growth by serving as the key connection between internal teams and external partners which will enable seamless execution and value delivery within Large Integrated Delivery Networks.</p><p>They Key Account Lead will build strong relationships across account customers including Pharmacy, P&T committee, multiple specialties, as well as operational and executive levels within the Account, establishing themselves as the primary contact for the Integrated Health System. Candidates need to be able to translate customer insights into actionable feedback to inform HQ colleagues; while addressing customer needs, support patient pull through, resolving issues, and ensure satisfaction throughout engagement lifecycle​ KAL’s need to be able to contribute to commercial strategy, product innovation, and market positioning.</p><h3>In this position a typical day may include the following:</h3><ul><li>Develop, establish, and actively lead the IDN / Healthcare account strategic Account Plan.</li><li>Participate in the development of new strategic marketing resources, foster key relationships within each account, work to implement key resources that improve patient diagnosis, timely treatment and outcomes in key Immunological diseases.</li><li>Engage and coordinate with patient support services to properly support pull-through at Health Systems at appropriate steps of engagement process.</li><li>Identify and remove barriers to collaboration to drive efficiency and accountability across teams​</li><li>Own the development of comprehensive account profiles capturing strategic priorities, customer mapping, and growth opportunities.</li><li>Analyze performance metrics, utilization trends, and customer feedback to generate insight.</li><li>Maintain a dynamic view of account engagements, using CRM tools and dashboards to monitor progress and inform future initiatives.</li></ul><p><strong>This May Be the Right Role for You If you:</strong></p><ul><li>You are capable of account profiling, planning, mapping and gap analysis,</li><li>You bring executive presence</li><li>You can effectively build relationships and facilitate Cross-functional Collaboration and influence, IDN / Healthcare System Expertise,</li><li>You are results oriented and customer-centric in approach.</li><li>You have experience in Respiratory / Immunology and leading others is strongly preferred but not required.</li></ul><p>To be considered for this role, will have a bachelor's degree and/or master's degree from an accredited college or university and a minimum of 12+ years of biopharmaceutical experience with primary focus in Field-Facing commercial roles such as Sales, Reimbursement, Account Management, Thought Leader Liaison, Market Access, District Manager, and other Commercial and/or Marketing roles. Strong preference for 3+ years of sales leadership experience and/or prior background in Respiratory / Immunology, Market Access, Account management experience calling on large academic centers, Integrated Health Networks, and C- suite level interactions a plus. . Must be willing to travel 50-70% (including weekend travel as needed). States in Mid-West IKAL geography include Michigan, Indiana and Ohio.</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>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 15:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Commercial Operations Lead]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45302]]></requisitionid>
    <referencenumber><![CDATA[R45302]]></referencenumber>
    <apijobid><![CDATA[r45302]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45302/director-commercial-operations-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Commercial Operations Lead to join our team in Munich, supporting our commercial business across the 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.</p><p>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><h3><strong>A Typical Day:</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 May Be For You:</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 value accuracy and clarity in communications, especially when supporting external teams.</p></li><li><p>You take pride in mentoring others and encouraging team growth.</p></li><li><p>You’re motivated by solving operational challenges that support patient-impacting work.</p></li></ul><p><strong>To be considered</strong></p><p>You’ll need to bring significant leadership experience in Commercial Operations within the German biopharmaceutical industry. A strong grasp of market dynamics, local laws, and reporting requirements is important. You should be confident navigating analytics, experienced with tools like PowerPoint, Excel, Veeva, and WORD, and able to communicate fluently in English. Prior experience supporting field sales in a pharma setting is desirable, along with a Bachelor’s degree and at least 7 years of industry experience, including 5 years in global commercial operations.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Statistical Genetics]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45056]]></requisitionid>
    <referencenumber><![CDATA[R45056]]></referencenumber>
    <apijobid><![CDATA[r45056]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45056/associate-manager-statistical-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[<p>We are seeking a highly motivated and talented Associate Manager, Analytical Genetics and Data Science (AGDS) to join the AGDS team at the Regeneron Genetics Center (RGC). In this individual contributor role, you will conduct analyses of large-scale human genetic and phenotypic datasets for the discovery and validation of new therapeutic targets. Your work will use both in-house and public data resources, and your responsibilities will include integrating genetic data with other multi-omics data, applying state of the art statistical tools and methodologies, performing QC, and identifying and interrogating data driven hypotheses related to analytic and translational genetics. In addition to designing and executing analytic studies, you will collaborate with groups across Regeneron’s R&D functions, including both pre-clinical and clinical development teams.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Demonstrated expertise in genetic association analyses using large-scale genetic data. </p></li><li><p>Strong understanding of multi-omic data integration and its application in therapeutic target discovery. </p></li><li><p>Experience in developing and implementing methods for data harmonization and normalization. </p></li><li><p>Experience with cutting edge genetic analysis approaches, such as genome-wide association analysis, exome-wide association analysis, rare variant analysis, Mendelian randomization, LD Score regression, polygenic risk score modelling, pleiotropy analysis, meta-analysis, and the use of functional data to prioritize variants and genes of interest.</p></li><li><p>Proven ability to independently lead and manage 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></ul><p><strong>This role might be for you if have:</strong></p><ul><li><p>A PhD in a relevant field (e.g., statistical genetics, bioinformatics, computational biology, genetics, or related disciplines). </p></li><li><p>0-2 years of post-PhD experience in analyzing large-scale omics datasets.</p></li><li><p>Outstanding communication skills and an ability to summarize and present the results of human genetic studies to a variety of technical audiences, ranging from specialists in statistical genetics and computation to specialists in biology, drug design, and medicine.</p></li></ul><p>​#RGC</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology - Garden City, NY]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45010]]></requisitionid>
    <referencenumber><![CDATA[R45010]]></referencenumber>
    <apijobid><![CDATA[r45010]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45010/medical-specialist-i-dermatology-garden-city-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[<h3><strong>Geography: Garden City, </strong><strong>NY</strong></h3><br><h3>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.</h3><br><h3><strong>As a Medical Specialist, a typical day may include the following:</strong></h3><ul><li><h3>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</h3></li><li><h3>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</h3></li><li><h3>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</h3></li><li><h3>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</h3></li><li><h3>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</h3></li></ul><br><h3><strong>This role may be for you if:</strong></h3><ul><li><h3>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</h3></li><li><h3>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</h3></li><li><h3>You have a competitive spirit and harness your “grit” to power your approach to sales</h3></li><li><h3>You collaborate effectively with internal and external partners</h3></li><li><h3>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</h3></li><li><h3>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</h3></li></ul><h3>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</h3><br><h3>#derm</h3><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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 08:56:53 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Field Medical Affairs - Respiratory (North Carolina, South Carolina)]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45746]]></requisitionid>
    <referencenumber><![CDATA[R45746]]></referencenumber>
    <apijobid><![CDATA[r45746]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45746/associate-director-field-medical-affairs-respiratory-north-carolina-south-carolina/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within Respiratory to support the clinical and business objectives across the product life cycle. We deliver strategic and operational support by establishing, developing and maintaining scientific exchange with medical specialists, health care professionals, and payers, aligned with our strategic objectives. We provide clinical and health economic information that enhances the value and appropriate use of Regeneron products. You will work with clinical research sites and investigators, and support of research activities as directed by the Global Medical Functional head.</p><p>Responsibilities of this role are to ensure accurate exchange and distribution of clinical and scientific information relevant to in-line and pipeline products in a timely, ethical and customer-focused manner.</p><p><strong>Territory:</strong> North Carolina/South Carolina</p><p><strong>A typical day may include</strong></p><p>•Engage in scientific discussions with medical and scientific specialists, including Healthcare Professionals and population health decision makers (“payers”) consistent with Medical Affairs objectives.</p><p>•Demonstrate deep scientific expertise related to assigned molecules/products and the associated therapeutic area to exchange relevant information and insights with specialists within a region.</p><p>•Build and develop relationships with key external scientific and medical specialists and organizations in a region to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape.</p><p>•Shape and execute local medical strategy based on Global Medical Affairs strategy within planned timelines.</p><p><strong>This may be for you if:</strong></p><p>•Enjoy working independently in the field, while having an impact on the company’s mission.</p><p>•You are passionate about developing knowledge of and sharing clinical scientific data.</p><p>•You like working collaboratively and developing relationships in academic and clinical practice settings.</p><p>•You have the innate ability to balance multiple initiatives, prioritize them and execute them independently, while excelling at keeping all partners advised and engaged.</p><p>To be considered for this position, you must have an advanced Clinical/Science Degree (e.g., MD, PharmD, PhD) with a minimum of 5 years related work experience (clinical, managed care, or industry experience). Experience as an MSL or in a Field Medical Affairs representative with Immunology is required. Respiratory experience is preferred, It is required to have the ability to communicate and disseminate scientific and clinical data. Residency in the territory is required.</p><p>#msl #medicalscienceliaison</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>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Lab Integration Developer]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45570]]></requisitionid>
    <referencenumber><![CDATA[R45570]]></referencenumber>
    <apijobid><![CDATA[r45570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45570/principal-it-lab-integration-developer/]]></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>The Principal IT Lab Integration Developer is responsible for designing, developing, validating, and supporting integrations between laboratory systems, analytical instruments, enterprise platforms (LIMS), and data platforms within a regulated pharmaceutical environment. This role combines application development, system integration, data management, and regulatory compliance within a GMP-regulated laboratory environment.</p><p>As a Principal IT Lab Integration Developer, a typical day might include the following:</p><ul><li>Support the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Design and develop integrations between instruments and the Orchestration Layer.</li><li>Build and support API-based, file-based, and message-based integrations (REST, SOAP, SFTP, JSON, XML).</li><li>Provide level 2/3 support for QC Lab Systems.</li><li>Partner with QC Analysts, QA, IT infrastructure and external vendors.</li><li>Develop instrument data capture and automation workflows.</li><li>Configure and support middleware and integration platforms.</li><li>Ensure all integrations comply with GxP, 21 CFR Part 11, and data integrity (ALCOA+) requirements.</li><li>Participate in Computer System Validation (CSV/CSA) activities (IQ/OQ/PQ documentation).</li><li>Perform impact assessments and change control documentation.</li><li>Monitor and troubleshoot integration issues in production environments.</li><li>Collaborate with QC, R&D, Manufacturing, and QA teams.</li><li>Support audits and regulatory inspections.</li></ul><p>This role may be for you if you have:</p><ul><li>Skill in connecting various lab instruments (e.g., liquid handlers, analyzers) to central platforms like LIMS or ELNs to automate data capture and reduce manual transcription.</li><li>Knowledge of RESTful APIs, web services, and middleware tools used to bridge communication between the orchestration engine and disparate lab hardware.</li><li>Proficiency in languages such as Python or VBA for customizing automated workflows and data parsing.</li><li>Ability to understand data formats across different systems, ensure consistent values/naming conventions, and providing the correct data to the authorized locations </li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology, Math or related field and 8 years of relevant experience or equivalent combination of education and experience.</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>$103,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Project Engineer]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45461]]></requisitionid>
    <referencenumber><![CDATA[R45461]]></referencenumber>
    <apijobid><![CDATA[r45461]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45461/associate-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>We are seeking an Associate Project Engineer who would design, specify and commission new and renovated biopharmaceutical process equipment. This role will provide engineering support and assist with problem solving for existing equipment and manufacturing processes.</p><p><strong>As an Associate Project Engineer, a typical day might include the following: </strong></p><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls</li><li>Managing small projects related to process equipment and manufacturing</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Preparing process and instrument drawings and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting validation department by preparation of design documents and assists in protocol execution</li><li>Assisting in investigations of process equipment and control system anomalies</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations for and executing modification change control documentation</li><li>May supervise mechanical, electrical, and automation contractors</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>Self-starter with high initiative and data-driven approach to problem-solving</li><li>Demonstrated strong interpersonal skills</li><li>You are able to prioritize, re-prioritize as needed and adapt to change</li><li>You have strong analytical and organizational skills</li><li>Demonstrated adaptability and flexibility to working in different environments, teams etc.</li></ul><p>To be considered for this position you should have a BEng or higher in Chemical, Process or Mechanical Engineering.</p><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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager-Dermatology-Columbus, OH]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45962]]></requisitionid>
    <referencenumber><![CDATA[R45962]]></referencenumber>
    <apijobid><![CDATA[r45962]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45962/reimbursement-business-manager-dermatology-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>Field Reimbursement Manager - Dermatology (Columbus, OH)</strong></p><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><p><strong>A typical day may include the following:</strong></p><ul><li><p>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.</p></li><li><p>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</p></li><li><p>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).</p></li><li><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p></li><li><p>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</p></li><li><p>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</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</p></li><li><p>You are an ethical, standout colleague and have can grow in a cross-functional team environment - contributing creative ideas and positive energy to the group.</p></li><li><p>You possess excellent organizational, project management, and communication skills.</p></li><li><p>Experience working with products delivered through a Specialty Pharmacy network is essential.</p></li><li><p>Collaboration and proactive communication skills.</p></li><li><p>Background in leadership and effective cross functional partnership a plus.</p></li><li><p>Established ability to work within an Account Management based structure.</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>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. Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors. Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation System Specialist]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43990]]></requisitionid>
    <referencenumber><![CDATA[R43990]]></referencenumber>
    <apijobid><![CDATA[r43990]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r43990/senior-automation-system-specialist/]]></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>As a Senior Automation System Specialist (Administrator), you will be embedded in a tight-knit team responsible for administration of automated/computerized system software and firmware to meet cGMP and policy requirements. In this critical role our team specifies and maintains software configuration for biopharmaceutical process, monitoring, and testing systems. This involves evaluation of new software for functional equivalence, validation activities to demonstrate suitability of software/process and maintaining the qualified state of systems throughout their lifecycle through change control.</p><p>In this role, a typical day might include:</p><ul><li><p>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</p></li><li><p>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</p></li><li><p>Utilizing configuration management and recipe/method management.</p></li><li><p>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</p></li><li><p>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</p></li><li><p>Conducting system integration with existing systems (e.g. LIMS, Historian).</p></li><li><p>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and/or design specifications, test plans, technical evaluation, and quality risk assessments.</p></li><li><p>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</p></li><li><p>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</p></li><li><p>Leading aspects of the work for contractors and providing guidance as applicable.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</p></li><li><p>Have interest in manufacturing process within a regulated technical environment.</p></li><li><p>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</p></li><li><p>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</p></li><li><p>Understand process control systems and product release testing systems.</p></li><li><p>Are familiar with regulatory and quality policies, procedures, documentation methods.</p></li><li><p>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</p></li><li><p>Enjoy project management and have strong organizational skills.</p></li><li><p>Are motivated to participate in continuous process improvement.</p></li></ul><p>Applicants ideally should have a BS/BA in Science, Engineering or related field and the following minimum relevant experience for each level:</p><ul><li><p>Senior Automation System Specialist (Administrator): 5+ years</p></li><li><p>Principal Automation System Specialist (Administrator): 8+ years</p></li></ul><p>Equivalent combination of education and experience may be considered. Level will be determined based on qualifications relevant to the role.</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>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industriebetrieb & Produktversorgung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Laboratory Assistant II]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45976]]></requisitionid>
    <referencenumber><![CDATA[R45976]]></referencenumber>
    <apijobid><![CDATA[r45976]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45976/laboratory-assistant-ii/]]></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 Lab Assistant to work with the operations team in the Bioreactor Scale Up and Development (BS&D) group, which is part of the Product Analytical and Process Development (PAPD) department. The operations team is primarily responsible for supporting routine laboratory tasks that are essential to BS&D core mission. This role will receive general instruction for routine work and will execute assigned tasks individually and in collaboration with others and will communicate primarily within the subgroup as well as other employees in the department.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><p>With guidance, perform routine tasks such as:</p><ul><li>Supporting lab operations to cultivate mammalian cells producing biologics in bench and pilot-scale bioreactors, including sterilizing, sanitizing, and operating bioreactors</li><li>Preparing media, buffers and feeds</li><li>Performing preventative maintenance activities and maintaining laboratory equipment</li><li>With guidance, troubleshoot bioreactor and equipment issues</li><li>Be flexible to support critical laboratory operations, including occasional weekend and off-hours work, to ensure the timely completion of process development studies and project deliverables.</li><li>Ensure that lab, storage, and hallway spaces are clean and organized to maintain safe working environment</li><li>Willingness to learn and adapt new laboratory practices (SOPs, protocols, procedures etc.) with supervision</li><li>Ability to multitask and prioritize tasks in a fast-paced laboratory environment.</li><li>With guidance, identify key process improvement opportunities and work to implement strategies to increase the speed and efficiency</li><li>Be adaptable to learning and supporting additional activities that may arise to continuously support BS&D and PMPD through future growth and expansion</li></ul><p><strong>This Role Might Be For You If You:</strong></p><ul><li>Possess good organization, communication, and collaboration skills; can work well within a team and individually</li><li>Have a service-oriented mindset and desire to provide quality customer service</li><li>Has an interest in science and strong attention to detail</li><li>Willingness to learn new tasks and responsibilities</li><li>Ability to lift and carry laboratory equipment and supplies as needed</li></ul><p>High School Diploma and 1-2 years of experience, or combination of training and experience. A 2-year college degree may be preferred. Experience in cell culture or media/buffer prep is a plus. </p><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 (hourly)</strong></strong></p>$26.35 - $41.15]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Analytical and Biological Mass Spectrometry]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45927]]></requisitionid>
    <referencenumber><![CDATA[R45927]]></referencenumber>
    <apijobid><![CDATA[r45927]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r45927/senior-scientist-analytical-and-biological-mass-spectrometry/]]></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>Regeneron Pharmaceutical's Analytical and Biological Mass Spectrometry Group (ABMS), located in Tarrytown, NY is seeking a highly motivated Sr. Scientist. In this role, you will work in an innovative mass spectrometry lab and develop LC-MS methods for characterizing biotherapeutic products to support all stages of drug development, from early-stage candidate selections to late-stage regulatory submissions. You will conduct and develop innovative technologies to support a diverse Regeneron's R&D pipeline.</p><p><strong>A Typical Day in This Role Looks Like:</strong></p><ul><li><p>Design, execute, and clearly communicate analytical characterization of biotherapeutics, including monoclonal and bispecific antibodies, Fc-fusion proteins, and other modalities (adeno-associated virus, siRNA, etc.) to support drug development.</p></li><li><p>Lead and execute characterization activities, with an emphasis on intact-mass LC-MS technique to elucidate critical quality attributes such as charge variants, size variants, and post-translational modifications.</p></li><li><p>Provide analytical support for cross-functional teams, including formulation development, upstream/downstream process development, and manufacturing to solve drug development challenges.</p></li><li><p>Advance LC-MS characterization of biotherapeutics by developing innovative techniques that address evolving developmental needs and improve operational efficiency.</p></li><li><p>Independently conduct sample preparation and LC-MS analyses in compliance with SOPs, and document experimental procedures and results in electronic laboratory notebook (ELN).</p></li><li><p>Author and review regulatory submission documents, including IND, comparability, and BLA reports, and contribute to manuscripts for peer-reviewed publications.</p></li><li><p>Represent analytical development on project teams, provide subject matter expertise, and communicate results at internal and external meetings.</p></li></ul><p><strong>This Role May Be for You If:</strong></p><ul><li><p>You thrive in a fast-paced, collaborative environment and consistently deliver results with efficiency and ownership.</p></li><li><p>You quickly learn new technologies, solve complex problems, and demonstrate strong passion for science and innovation.</p></li><li><p>You are self-motivated and proactive, with the ability to prioritize effectively and drive work forward with minimal supervision.</p></li></ul><p><strong>To be considered for this role,</strong> <strong>you must have</strong> an MS (2+ years) or PhD degree (0-2+ years) in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related field. Extensive experience with advanced mass spectrometers (Q Exactive Plus, Q Exactive UHMR, Q-TOF, etc.), liquid chromatography, and data processing software (Skyline, Protein Metrics, etc.) is desired. Experience with extended characterization of monoclonal antibodies by mass spectrometry to support product and process development is a plus. Experience with automated liquid-handling systems (e.g., Bravo, KingFisher) and with experimental design and data analysis (e.g., design of experiments, molecular modeling, graphing, and statistical analysis software such as JMP) is a plus.</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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 19:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Allergy/ENT) - San Antonio, Texas]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46124]]></requisitionid>
    <referencenumber><![CDATA[R46124]]></referencenumber>
    <apijobid><![CDATA[r46124]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46124/medical-specialist-i-allergyent-san-antonio-texas/]]></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>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists as well as 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, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</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>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 may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p><strong>Geography: San Antonio, TX</strong></p><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role<strong>. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories. </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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 12:26:21 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46220]]></requisitionid>
    <referencenumber><![CDATA[R46220]]></referencenumber>
    <apijobid><![CDATA[r46220]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r46220/senior-manager-clinical-scientist-hematology/]]></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>The Senior Manager, Hematology, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>As a Senior Manager in Hematology Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Develops/maintains 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>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Exhibits strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. We are seeking proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements. Considerable organizational awareness, including significant experience working cross-functionally. Other levels considered depending on experience. #Hematology</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>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Globale Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Assoc Scientist- Biomolecular Interactions/Kinetics]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41252]]></requisitionid>
    <referencenumber><![CDATA[R41252]]></referencenumber>
    <apijobid><![CDATA[r41252]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r41252/sr-assoc-scientist-biomolecular-interactionskinetics/]]></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>We are seeking a motivated Sr Assoc Scientist to join the High Throughput Antibody Screening and Biomolecular Interaction Group within the Therapeutic Proteins team.</strong> You will support Therapeutics Protein activities by implementing methods to characterize protein interaction kinetics and biochemical properties using SPR, BLI, ITC, and other analytical technologies in support of our VelocImmune fully-human antibody pipeline.</p><p><strong>As a Sr Assoc Scientist, a typical day might include:</strong></p><ul><li><p>Conducting experiments including antibody characterization, method development, and analytical support for biologics development using biochemical and biophysical methods</p></li><li><p>Troubleshooting established test methods used in development and release testing of screening reagents</p></li><li><p>Tabulating results and writing summary reports of assay development</p></li><li><p>Presenting findings at group and interdepartmental meetings</p></li><li><p>Maintaining lab supplies and equipment</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Can work independently, show initiative to design and carry out experiments based on protocols</p></li><li><p>Manage and organize data independently, as well as have decision-making capabilities but know when to reach out for support</p></li><li><p>Can troubleshoot methodological and technical issues</p></li><li><p>Enjoy working in a fast-paced and deadline driven team environment and are capable of multi-tasking across assignments</p></li><li><p>Have excellent communication skills</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS with 4+ years of relevant lab experience. We need someone with a foundational knowledge in structural biology, biophysics, or chemical biology. Must have experience in protein chemistry techniques (HPLC, FLPC, ion-exchange, affinity, size exclusion chromatography, and protein conjugation chemistry) and protein analysis (SDS-PAGE, Western-blot, ELISA). Knowledge and experience in using biophysical methodologies such as Biacore, Octet, or ITC to study protein/small molecule or protein/protein interactions and binding kinetics is required.</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>$79,100.00 - $129,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Forschung & präklinische Entwicklung]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Canada]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46239]]></requisitionid>
    <referencenumber><![CDATA[R46239]]></referencenumber>
    <apijobid><![CDATA[r46239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/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>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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Unternehmensfunktionen]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology -  Kansas]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44977]]></requisitionid>
    <referencenumber><![CDATA[R44977]]></referencenumber>
    <apijobid><![CDATA[r44977]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/de/stellen/r44977/medical-specialist-i-dermatology-kansas/]]></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[<p><strong>Geography: Kansas</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>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</li><li>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</li><li>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>You have a competitive spirit and harness your “grit” to power your approach to sales</li><li>You collaborate effectively with internal and external partners</li><li>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>You 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. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. 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. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments.This role requires the ability to travel and cover large geographic territories. This role requires the ability to travel and cover large geographic territories. To be considered for this role, candidates must reside within the listed territory.</p><p>#derm</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>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Kommerziell]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
</source>